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        <title>Current Osteoporosis Reports via MedWorm.com</title>
        <description>MedWorm.com provides a medical RSS filtering service. Over 6000 RSS medical sources are combined and output via different filters. This feed contains the latest items from the 'Current Osteoporosis Reports' source.</description>
        <link><![CDATA[http://www.medworm.com/rss/search.php?qu=Current+Osteoporosis+Reports&t=Current+Osteoporosis+Reports&s=Search&f=source]]></link>
        <lastBuildDate>Fri, 19 Mar 2010 16:06:03 +0100</lastBuildDate>
        <item>
            <title>Intravenous Zoledronic Acid: What Are the Indications for Male Osteoporosis?</title>
            <link>http://www.medworm.com/index.php?rid=3361211&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh7n787k45582w30q%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Osteoporosis and fractures are under-recognized and undertreated, both in men and women worldwide. Male osteoporosis is not
 the epidemic problem that female osteoporosis is; however, the National Osteoporosis Foundation estimates that over 14 million
 American men have osteoporosis or low bone mass, and approximately 25% to 30% of all hip fractures occur in male individuals
 who incur greater morbidity and mortality than their female counterparts. Until recently, alendronate, risedronate, and teriparatide
 were the only pharmacologic agents approved by the US Food and Drug Administration for treating male osteoporosis. In December
 2008, zoledronic acid was approved for “treatment to increase bone mass in men with osteoporosis.” In 2009, zoledronic acid
 was also a...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3361211</comments>
            <pubDate>Thu, 11 Mar 2010 02:24:30 +0100</pubDate>
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        <item>
            <title>Atypical Subtrochanteric and Femoral Shaft Fractures and Possible Association with Bisphosphonates</title>
            <link>http://www.medworm.com/index.php?rid=3329320&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj5118q2572108660%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Several case series and multiple individual case reports suggest that some subtrochanteric and femoral shaft fractures might
 occur in patients who have been treated with long-term bisphosphonates. Several unique clinical and radiographic features
 are emerging: prodromal thigh pain prior to the fracture, complete absence of trauma precipitating the fracture, and bilateral
 fractures in some patients. Radiographic features include presence of stress reaction, transverse or short oblique fractures,
 and thick femoral cortices. The overall incidence of subtrochanteric and shaft fractures combined is below 30 per 100,000
 person-years, so this type of fracture is much less common than proximal femur (hip) fracture. Furthermore, the unique “atypical”
 fracture type is a...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3329320</comments>
            <pubDate>Tue, 02 Mar 2010 10:08:05 +0100</pubDate>
            <guid isPermaLink="false">3329320</guid>        </item>
        <item>
            <title>Orthopedic Uses of Teriparatide</title>
            <link>http://www.medworm.com/index.php?rid=3329321&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F9440854572p08182%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Teriparatide is a drug currently approved for treating patients with osteoporosis who are at high risk for future fracture.
 In the treatment of osteoporosis, teriparatide works as an anabolic agent stimulating bone formation throughout the skeleton
 by principally enhancing osteoblast-derived bone formation relative to osteoclast-derived bone resorption. The net effect
 is increased bone mass. For patients with a fracture, a similar process of increased bone formation is required transiently
 at the fracture site for repair. Teriparatide has been investigated in animal models and in patients as a potential agent
 to enhance fracture repair. In addition, evidence that teriparatide enhances chondrogenesis has generated interest in using
 the agent for articular cartilage...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3329321</comments>
            <pubDate>Tue, 02 Mar 2010 10:08:03 +0100</pubDate>
            <guid isPermaLink="false">3329321</guid>        </item>
        <item>
            <title>Is Osteoporosis Disease Management Cost Effective?</title>
            <link>http://www.medworm.com/index.php?rid=3296646&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F9674014257781658%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Can osteoporosis disease management be cost effective? To answer that question, we conducted an extensive review of osteoporosis
 and fragility fracture prevention literature in peer-reviewed scientific journals and evidence-based guidelines from professional
 societies and government health organizations. We explored different strategies suggested by the literature to find how programs
 can be structured to be cost effective and to decrease fracture rates. We focused on ways to cost effectively identify, risk
 stratify, treat, and then track patients at risk for osteoporosis and fragility fractures. Studies have shown that osteoporosis
 management can decrease the hip fracture rate by 25% to 50% and be cost effective at the same time.
 
 
	Content Type Journal ArticleD...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3296646</comments>
            <pubDate>Sat, 20 Feb 2010 06:57:45 +0100</pubDate>
            <guid isPermaLink="false">3296646</guid>        </item>
        <item>
            <title>Glucocorticoid-Induced Osteoporosis: Management Update</title>
            <link>http://www.medworm.com/index.php?rid=3291654&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu821088017355002%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Osteoporosis due to glucocorticoid-induced osteoporosis (GIOP) for inflammatory disorders continues to be a common problem.
 Well-distributed guidelines have provided evidence-based recommendations for management, yet many patients have little attention
 paid to their increased fracture risk. The purpose of this article is to discuss how new treatments for GIOP may improve overall
 management. Intravenous zoledronic acid (ZA), an antiresorptive agent, and teriparatide (TPT), which stimulates osteoblasts,
 have received US Food and Drug Administration (FDA) approval for treating GIOP. ZA is appealing because one 15-min infusion
 covers the patient for a year and potentially will increase the proportion of GIOP patients who are treated. TPT makes physiologic
 sense becaus...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3291654</comments>
            <pubDate>Fri, 19 Feb 2010 06:44:44 +0100</pubDate>
            <guid isPermaLink="false">3291654</guid>        </item>
        <item>
            <title>Benefits and Limitations of Bone Mineral Density and Bone Turnover Markers to Monitor Patients Treated for Osteoporosis</title>
            <link>http://www.medworm.com/index.php?rid=3291653&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc368054401034550%2F</link>
            <description>This article reviews the clinical use and abuse of the two biomarkers most commonly
 used to assess the effectiveness of therapy in clinical practice: bone mineral density testing and measurement of markers
 of bone turnover.
 
 
	Content Type Journal ArticleDOI 10.1007/s11914-010-0004-5Authors
		E. Michael Lewiecki, New Mexico Clinical Research &amp; Osteoporosis Center 300 Oak Street NE Albuquerque NM 87106 USA
	

	
		Journal Current Osteoporosis ReportsOnline ISSN 1544-2241Print ISSN 1544-1873 (Source: Current Osteoporosis Reports)</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3291653</comments>
            <pubDate>Fri, 19 Feb 2010 06:44:44 +0100</pubDate>
            <guid isPermaLink="false">3291653</guid>        </item>
        <item>
            <title>Anabolic Therapies</title>
            <link>http://www.medworm.com/index.php?rid=3289746&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F3015288l71616336%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The striking clinical benefits of intermittent parathyroid hormone in osteoporosis have begun a new era of skeletal anabolic
 agents. Recombinant human parathyroid hormone (rhPTH) (1–34) is the first US Food and Drug Administration–approved anabolic
 therapy. Its use has been limited by the need for subcutaneous injection. Newer delivery systems include transdermal and oral
 preparations. Newer anabolic therapies include monoclonal antibody to sclerostin, a potent inhibitor of osteoblastogenesis;
 and use of bone morphogenetic proteins and parathyroid hormone–related protein PTHrP, a calcium-regulating hormone similar
 to PTH.
 
 
	Content Type Journal ArticleDOI 10.1007/s11914-010-0005-4Authors
		Nancy E. Lane, University of California at Davis Medical Center Agi...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3289746</comments>
            <pubDate>Thu, 18 Feb 2010 06:53:05 +0100</pubDate>
            <guid isPermaLink="false">3289746</guid>        </item>
        <item>
            <title>The Role of Microbial Biofilms in Osteonecrosis of the Jaw Associated with Bisphosphonate Therapy</title>
            <link>http://www.medworm.com/index.php?rid=3289748&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F2100p71804m7t122%2F</link>
            <description>This article explains the role of microbial
 biofilms in BONJ and also discusses associated factors in the disease pathogenesis, which include BP effects on bone remodeling,
 anti-angiogenesis, matrix necrosis, microcracks, soft tissue toxicity, and inflammation and wound healing. Recent findings
 suggest a key role for microbial biofilms in the pathogenesis of BONJ; this has important therapeutic implications because
 biofilm organisms represent a clinical target for prevention and treatment efforts aimed at reducing the significant morbidity
 and costs associated with this condition.
 
 
	Content Type Journal ArticleDOI 10.1007/s11914-010-0008-1Authors
		Satish K. S. Kumar, University of Southern California Clinical Dentistry, Orofacial Pain and Oral Medicine Center, Division of Diagnost...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3289748</comments>
            <pubDate>Thu, 18 Feb 2010 06:53:04 +0100</pubDate>
            <guid isPermaLink="false">3289748</guid>        </item>
        <item>
            <title>Denosumab Reduces the Incidence of New Vertebral Fractures in Men With Prostate Cancer</title>
            <link>http://www.medworm.com/index.php?rid=3289747&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa678n04735856347%2F</link>
            <description>Content Type Journal ArticleCategory CLINICAL TRIAL REPORTDOI 10.1007/s11914-010-0001-8Authors
		David S. Silver, Cedars Sinai Medical Center/UCLA School of Medicine and the OMC Clinical Research Center 8641 Wilshire Boulevard, Suite 301 Beverly Hills CA 90211 USA
	

	
		Journal Current Osteoporosis ReportsOnline ISSN 1544-2241Print ISSN 1544-1873 (Source: Current Osteoporosis Reports)</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3289747</comments>
            <pubDate>Thu, 18 Feb 2010 06:53:04 +0100</pubDate>
            <guid isPermaLink="false">3289747</guid>        </item>
        <item>
            <title>Early life factors in the pathogenesis of osteoporosis</title>
            <link>http://www.medworm.com/index.php?rid=3042263&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl30k38k4wv857t68%2F</link>
            <description>This article describes the latest data in this exciting area of research, including novel epigenetic and translation work,
 which should help to elucidate the underlying mechanisms and give rise to potential public health interventions to reduce
 the burden of osteoporotic fracture in future generations.
 
	Content Type Journal ArticleDOI 10.1007/s11914-009-0024-1Authors
		Chivon WinsloeSusie EarlElaine M. DennisonCyrus CooperNicholas C. Harvey, University of Southampton, School of Medicine, Southampton General Hospital Medical Research Council Epidemiology Resource Centre Southampton SO16 6YD UK
	

	
		Journal Current Osteoporosis ReportsOnline ISSN 1544-2241Print ISSN 1544-1873
	
		Journal Volume Volume 7
	
		Journal Issue Volume 7, Number 4 / December, 2009 (Source: Current Osteoporosis...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3042263</comments>
            <pubDate>Sun, 29 Nov 2009 09:37:08 +0100</pubDate>
            <guid isPermaLink="false">3042263</guid>        </item>
        <item>
            <title>Bone loss or lost bone: Rationale and recommendations for the diagnosis and treatment of early postmenopausal bone loss</title>
            <link>http://www.medworm.com/index.php?rid=3042262&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fvt62n015k318763x%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Recent reports suggest that bone loss begins during late perimenopause at a dramatic rate, even before estrogen levels plummet.
 During the ensuing 5 years, there is evidence of the beginnings of microarchitectural deterioration, which impacts bone strength
 and ultimately enhances its propensity to fracture. The diagnosis of osteoporosis based on T-scores alone, or through stratification
 for a high fracture risk by FRAX, excludes these women who are rapidly losing bone. Because all antiosteoporosis therapies,
 in particular bisphosphonates, reduce bone loss, we propose aggressive, likely short-term therapy with a goal to reduce bone
 loss, stabilize bone density, and prevent microarchitectural deterioration.
 
	Content Type Journal ArticleDOI 10.1007/s11914-009-0021-4...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3042262</comments>
            <pubDate>Sun, 29 Nov 2009 09:37:08 +0100</pubDate>
            <guid isPermaLink="false">3042262</guid>        </item>
        <item>
            <title>Osteoporosis prevention and nutrition</title>
            <link>http://www.medworm.com/index.php?rid=3042265&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F3p173x6326132838%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Although calcium and vitamin D have been the primary focus of nutritional prevention of osteoporosis, recent research has
 clarified the importance of several additional nutrients and food constituents. Further, results of calcium and vitamin D
 supplementation trials have been inconsistent, suggesting that reliance on this intervention may be inadequate. In addition
 to dairy, fruit and vegetable intake has emerged as an important modifiable protective factor for bone health. Several nutrients,
 including magnesium, potassium, vitamin C, vitamin K, several B vitamins, and carotenoids, have been shown to be more important
 than previously realized. Rather than having a negative effect on bone, protein intake appears to benefit bone status, particularly
 in older adults....</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3042265</comments>
            <pubDate>Sun, 29 Nov 2009 09:37:07 +0100</pubDate>
            <guid isPermaLink="false">3042265</guid>        </item>
        <item>
            <title>Proinflammatory cytokines and osteoporosis</title>
            <link>http://www.medworm.com/index.php?rid=3042264&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fbl883u86q08m5523%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Experimental studies indicate that the proinflammatory cytokines interleukin-1, interleukin-6, and tumor necrosis factor-α
 are important regulators of bone resorption and may play an important role in age- and estrogen deficiency-related bone loss.
 Although the observation of accelerated bone loss in patients with inflammatory disorders supports this mechanism, the role
 of cytokines in the etiology of osteoporosis has yet to be determined. Elucidation of this potential relationship could not
 only provide clinicians with an additional tool to identify patients at risk for osteoporosis, but may also inform the development
 of cytokine-blocking therapies as potential interventions to curb bone loss. Although some epidemiologic studies suggest increases
 in proinflamma...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3042264</comments>
            <pubDate>Sun, 29 Nov 2009 09:37:07 +0100</pubDate>
            <guid isPermaLink="false">3042264</guid>        </item>
        <item>
            <title>Variation in risk factors for fractures at different sites</title>
            <link>http://www.medworm.com/index.php?rid=3042266&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fjn200365g6237h6h%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Fractures in older people are important medical problems. Knowledge of risk factors is essential for successful preventive
 measures, but when fracture sites of diverse etiology are combined, risk factors for any one site are difficult to identify
 and may be missed entirely. Among older people, incidence rates of hip, proximal humerus, and vertebral fractures increase
 with age, but not rates of distal forearm and foot fractures. Low bone mineral density is strongly associated with hip, distal
 forearm, vertebral, and proximal humerus fractures, but not foot fracture. Most fractures of the hip, distal forearm, and
 proximal humerus result from a fall, whereas smaller proportions of fractures of the foot and vertebrae follow a fall. Frail
 people are likely to fracture ...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3042266</comments>
            <pubDate>Sun, 29 Nov 2009 09:37:06 +0100</pubDate>
            <guid isPermaLink="false">3042266</guid>        </item>
        <item>
            <title>Beneficial effects of denosumab for reducing risk of vertebral and nonvertebral fractures</title>
            <link>http://www.medworm.com/index.php?rid=3042267&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F2t08288763828050%2F</link>
            <description>Content Type Journal ArticleDOI 10.1007/s11914-009-0025-0Authors
		Chin Lee, Northwestern Feinberg School of Medicine and Abbott Laboratories Chicago USA
	

	
		Journal Current Osteoporosis ReportsOnline ISSN 1544-2241Print ISSN 1544-1873
	
		Journal Volume Volume 7
	
		Journal Issue Volume 7, Number 4 / December, 2009 (Source: Current Osteoporosis Reports)</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3042267</comments>
            <pubDate>Sun, 29 Nov 2009 09:37:05 +0100</pubDate>
            <guid isPermaLink="false">3042267</guid>        </item>
        <item>
            <title>New therapies for osteoporosis: Zoledronic acid, bazedoxifene, and denosumab</title>
            <link>http://www.medworm.com/index.php?rid=2767703&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fph6142240mg7m3k7%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Intravenous (IV) zoledronic acid, a new once-yearly bisphosphonate therapy, is approved by the US Food and Drug Administration
 for treatment of postmenopausal osteoporosis, glucocorticoid-induced osteoporosis, and osteoporosis in men. IV zoledronic
 acid significantly reduced the risk of vertebral, nonvertebral, and hip fractures in postmenopausal women and decreased risk
 of clinical fracture and clinical vertebral fracture in men and women with hip fracture. Two promising new therapies are in
 late clinical development. Denosumab is a monoclonal receptor activator of nuclear factor-κB ligand (RANKL) antibody given
 by subcutaneous injection every 6 months that has been shown to significantly reduce risk of vertebral-, nonvertebral-, and
 hip fracture in postmenopaus...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2767703</comments>
            <pubDate>Thu, 03 Sep 2009 06:07:53 +0100</pubDate>
            <guid isPermaLink="false">2767703</guid>        </item>
        <item>
            <title>From relative risk to absolute fracture risk calculation: The FRAX algorithm</title>
            <link>http://www.medworm.com/index.php?rid=2767705&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F6838265u44451337%2F</link>
            <description>This article describes the steps undertaken
 in the development of FRAX.
 
	Content Type Journal ArticleDOI 10.1007/s11914-009-0013-4Authors
		Eugene V. McCloskey, University of Sheffield, Sorby Wing, Northern General Hospital World Health Organization Collaborating Centre for Metabolic Bone Diseases Herries Road Sheffield S5 7AU UKHelena JohanssonAnders OdenJohn A. Kanis
	

	
		Journal Current Osteoporosis ReportsOnline ISSN 1544-2241Print ISSN 1544-1873
	
		Journal Volume Volume 7
	
		Journal Issue Volume 7, Number 3 / September, 2009 (Source: Current Osteoporosis Reports)</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2767705</comments>
            <pubDate>Thu, 03 Sep 2009 06:07:52 +0100</pubDate>
            <guid isPermaLink="false">2767705</guid>        </item>
        <item>
            <title>Strontium ranelate: New data on fracture prevention and mechanisms of action</title>
            <link>http://www.medworm.com/index.php?rid=2767704&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fnh86870645g8w145%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Osteoporosis treatments need to combine an unequivocally demonstrated reduction of fractures, at various skeletal sites, long-term
 safety, and a user-friendly profile that optimizes therapeutic adherence. Strontium ranelate is the first compound to simultaneously
 decrease bone resorption and stimulate bone formation. Its anti-fracture efficacy at various skeletal sites has been established
 for as long as 5 years through studies of the highest methodological standards. Increases in bone mineral density observed
 after 1 year of treatment are predictive of the long-term fracture efficacy, suggesting for the first time in osteoporosis
 that bone densitometry can be used as a monitoring tool. Due to a positive risk/benefit ratio, strontium ranelate is now considered
 as ...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2767704</comments>
            <pubDate>Thu, 03 Sep 2009 06:07:52 +0100</pubDate>
            <guid isPermaLink="false">2767704</guid>        </item>
        <item>
            <title>Glucocorticoid-induced osteoporosis: An indication for anabolic therapy</title>
            <link>http://www.medworm.com/index.php?rid=2767707&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fd7236n2606316rg5%2F</link>
            <description>Content Type Journal ArticleCategory Clinical Trials ReportDOI 10.1007/s11914-009-0018-zAuthors
		Piet Geusens, University Hasselt Biomedical Research Institute Hasselt Belgium
	

	
		Journal Current Osteoporosis ReportsOnline ISSN 1544-2241Print ISSN 1544-1873
	
		Journal Volume Volume 7
	
		Journal Issue Volume 7, Number 3 / September, 2009 (Source: Current Osteoporosis Reports)</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2767707</comments>
            <pubDate>Thu, 03 Sep 2009 06:07:51 +0100</pubDate>
            <guid isPermaLink="false">2767707</guid>        </item>
        <item>
            <title>Clinical relevance of diagnosing vertebral fractures by vertebral fracture assessment</title>
            <link>http://www.medworm.com/index.php?rid=2767706&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm722704813m82951%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Low bone mineral density and the presence of vertebral fractures are independent predictors for future vertebral and non-vertebral
 fractures. Combining the conventional measurement of bone mineral density of spine and hips with the morphometry of the thoracal
 and lumbar vertebrae on lateral images using dual energy x-ray absorptiometry scanners, a technique called vertebral fracture
 assessment, facilitates detection of vertebral fractures in those patients at older age and with clinical risk factors for
 osteoporosis. Particularly, the finding of one or more vertebral deformities in patients with osteopenia is clinically important,
 because this might prompt the start of anti-osteoporotic treatment.
 
	Content Type Journal ArticleDOI 10.1007/s11914-009-0017-0Authors
...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2767706</comments>
            <pubDate>Thu, 03 Sep 2009 06:07:51 +0100</pubDate>
            <guid isPermaLink="false">2767706</guid>        </item>
        <item>
            <title>Bone markers in osteoporosis</title>
            <link>http://www.medworm.com/index.php?rid=2767708&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv732673305416qu3%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Current biological markers of bone turnover have proven useful in improving fracture risk assessment and monitoring treatment
 efficacy in postmenopausal osteoporosis. Recent developments in the field of bone markers include 1) identification of new
 biochemical markers providing additional information on the complex pathways leading to bone fragility; 2) application of
 novel technologies such as proteomics for the discovery of novel markers; 3) automation and multiplexing for improving analytical
 performance and convenience; and 4) refinement of the clinical interpretation of markers. Currently, however, for the management
 of individual patients, their most established application is to monitor treatment efficacy and possibly to improve fracture
 risk assessment. Th...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2767708</comments>
            <pubDate>Thu, 03 Sep 2009 06:07:49 +0100</pubDate>
            <guid isPermaLink="false">2767708</guid>        </item>
        <item>
            <title>Can healthy, older, nonosteoporotic men benefit from calcium supplementation?</title>
            <link>http://www.medworm.com/index.php?rid=2767709&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc4057821766606g4%2F</link>
            <description>Content Type Journal ArticleCategory Clinical Trials ReportDOI 10.1007/s11914-009-0019-yAuthors
		Chin Lee, 200 Abbott Park Road Department NJ44, Building AP6C-6 Abbott Park IL 60064 USA
	

	
		Journal Current Osteoporosis ReportsOnline ISSN 1544-2241Print ISSN 1544-1873
	
		Journal Volume Volume 7
	
		Journal Issue Volume 7, Number 3 / September, 2009 (Source: Current Osteoporosis Reports)</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2767709</comments>
            <pubDate>Thu, 03 Sep 2009 06:07:48 +0100</pubDate>
            <guid isPermaLink="false">2767709</guid>        </item>
        <item>
            <title>Wnt signaling during fracture repair</title>
            <link>http://www.medworm.com/index.php?rid=2643396&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F285n866631230710%2F</link>
            <description>This article reviews
 recent data demonstrating that Wnt pathways are active during fracture repair and that increasing the activities of Wnt pathway
 components accelerates bone regeneration.
 
	Content Type Journal ArticleDOI 10.1007/s11914-009-0012-5Authors
		Frank J. SecretoLuke H. HoeppnerJennifer J. Westendorf, Mayo Clinic Departments of Orthopedic Surgery and Biochemistry &amp; Molecular Biology 200 First Street SW Rochester MN 55905 USA
	

	
		Journal Current Osteoporosis ReportsOnline ISSN 1544-2241Print ISSN 1544-1873
	
		Journal Volume Volume 7
	
		Journal Issue Volume 7, Number 2 / July, 2009 (Source: Current Osteoporosis Reports)</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2643396</comments>
            <pubDate>Sat, 25 Jul 2009 03:57:11 +0100</pubDate>
            <guid isPermaLink="false">2643396</guid>        </item>
        <item>
            <title>Assessment of material, structural, and functional properties of the human skeleton by pQCT systems</title>
            <link>http://www.medworm.com/index.php?rid=2643398&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F1p1587h734716856%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Peripheral quantitative computed tomography (pQCT) systems measure bone parameters noninvasively using low radiation doses.
 This limits image resolution but is practical for the diagnosis and quantitative monitoring of the properties of the peripheral
 human skeleton. pQCT determines volumetric bone mineral density separately in trabecular and cortical bone. It may combine
 densitometry determinations with geometric estimates and use strain-stress indexes, and it may be used to analyze muscle variables
 in some areas, allowing the study of regional fragility. Experimental and clinical ex vivo studies show that pQCT variables
 correlate with biomechanical predictors of fragility and/or fractures. Since pQCT was approved by the US Food and Drug Administration
 in 1997, n...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2643398</comments>
            <pubDate>Sat, 25 Jul 2009 03:57:09 +0100</pubDate>
            <guid isPermaLink="false">2643398</guid>        </item>
        <item>
            <title>Mechanisms linking osteoporosis with cardiovascular calcification</title>
            <link>http://www.medworm.com/index.php?rid=2643397&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F9l513k0485036603%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Cardiovascular calcium deposition is associated with osteoporosis through various potential mechanisms involving molecular
 regulatory factors at the nanoscale level that govern skeletal bone and cardiovascular tissues. In this article, several possible
 mechanisms linking cardiovascular calcification and osteoporosis are discussed, including aging, tissue-specific responses
 to chronic inflammation, flow-limiting atherosclerosis of skeletal end arteries causing ischemic abnormalities in metabolism,
 shared endogenous regulatory factors that affect the two tissues in a reciprocal manner, and changes in a cysteine protease
 inhibitor, fetuin. Any or all of these factors and phenomena may contribute to the association.
 
	Content Type Journal ArticleDOI 10.1007/s11914-009...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2643397</comments>
            <pubDate>Sat, 25 Jul 2009 03:57:09 +0100</pubDate>
            <guid isPermaLink="false">2643397</guid>        </item>
        <item>
            <title>Vitamin D and immune function: Understanding common pathways</title>
            <link>http://www.medworm.com/index.php?rid=2643399&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg71577r612263824%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Vitamin D, acting through its active metabolite 1,25(OH)2D3, exerts its influence on many physiologic processes in addition to the regulation of calcium and phosphate homeostasis. These
 processes include the immune system. Both the adaptive and innate immune systems are affected by 1,25(OH)2D3 and its receptor, and the cells involved express not only the vitamin D receptor but also, in most cases, the enzyme CYP27B1,
 which produces 1,25(OH)2D3. Both the vitamin D receptor and CYP27B1 can be constitutive or induced by the ligands that activate the immune processes
 in these cells, providing feedback loops that help regulate the immune response. In general, 1,25(OH)2D3 suppresses most elements of the adaptive immune system while inducing most elements of the innate immu...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2643399</comments>
            <pubDate>Sat, 25 Jul 2009 03:57:08 +0100</pubDate>
            <guid isPermaLink="false">2643399</guid>        </item>
        <item>
            <title>The influence of parathyroid hormone on the adult hematopoietic stem cell niche</title>
            <link>http://www.medworm.com/index.php?rid=2643401&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fpu488318765064h8%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Adult hematopoietic stem cells (HSCs) reside in the bone marrow in stable microenvironments known as the stem cell niche.
 One key component of the stem cell niche is cells of the osteoblastic lineage. Factors that are known to affect osteoblast
 activity, such as parathyroid hormone (PTH), have also been shown to affect the HSCs. Treatment of mice with PTH has led to
 beneficial effects on the HSC pool, which have led to clinical trials of PTH treatment to enhance HSC-based therapies.
 
	Content Type Journal ArticleDOI 10.1007/s11914-009-0010-7Authors
		Narges RashidiGregor B. Adams, University of Southern California Eli and Edythe Broad Center for Regenerative Medicine and Stem Cell Research at University of Southern California, Keck School of Medicine 1450 Biggy Stre...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2643401</comments>
            <pubDate>Sat, 25 Jul 2009 03:57:06 +0100</pubDate>
            <guid isPermaLink="false">2643401</guid>        </item>
        <item>
            <title>Thyroid-stimulating hormone, thyroid hormones, and bone loss</title>
            <link>http://www.medworm.com/index.php?rid=2643400&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fpwq81868w9657455%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;It has become accepted by virtue of rich anecdotal experience and clinical research that thyrotoxicosis is associated with
 high-turnover osteoporosis. The bone loss, primarily due to accelerated resorption that is not compensated by a coupled increase
 in bone formation, has been attributed solely to elevated thyroid hormone levels. Evidence using mice lacking the thyroid
 hormone receptors α and β establishes a role for thyroid hormones in regulating bone remodeling but does not exclude an independent
 action of thyroid-stimulating hormone (TSH), levels of which are low in hyperthyroid states, even when thyroid hormones are
 normal, as after thyroxine supplementation and in subclinical hyperthyroidism. We show that TSH directly suppresses bone remodeling
 and that T...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2643400</comments>
            <pubDate>Sat, 25 Jul 2009 03:57:06 +0100</pubDate>
            <guid isPermaLink="false">2643400</guid>        </item>
        <item>
            <title>B vitamins, homocysteine, and bone disease: Epidemiology and pathophysiology</title>
            <link>http://www.medworm.com/index.php?rid=2371860&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F0576n58k730111q4%2F</link>
            <description>This article reviews the connections of homocysteine and
 B vitamins to measures of bone quality and osteoporotic fracture. Although the literature suggests that these factors may
 be associated with bone health, most of the epidemiologic studies are observational, limiting conclusions regarding causality.
 More controlled trials are needed to determine whether treatment with B vitamins would reduce fracture rates among community-dwelling
 cohorts.
 
	Content Type Journal ArticleDOI 10.1007/s11914-007-0026-9Authors
		Robert R. McLean, Hebrew SeniorLife Institute for Aging Research 1200 Centre Street Boston MA 02131 USAMarian T. Hannan
	

	
		Journal Current Osteoporosis ReportsOnline ISSN 1544-2241Print ISSN 1544-1873
	
		Journal Volume Volume 5
	
		Journal Issue Volume 5, Number 3 / Septe...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2371860</comments>
            <pubDate>Sun, 26 Apr 2009 05:56:15 +0100</pubDate>
            <guid isPermaLink="false">2371860</guid>        </item>
        <item>
            <title>The RANKL/RANK/OPG pathway</title>
            <link>http://www.medworm.com/index.php?rid=2371859&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F8v472k3k8l738806%2F</link>
            <description>This article reviews the roles of the RANKL/RANK/OPG system in bone and other tissues.
 
	Content Type Journal ArticleDOI 10.1007/s11914-007-0024-yAuthors
		Brendan F. Boyce, University of Rochester Medical Center Department of Pathology and Laboratory Medicine 601 Elmwood Avenue Box 626 Rochester NY 14642 USALianping Xing
	

	
		Journal Current Osteoporosis ReportsOnline ISSN 1544-2241Print ISSN 1544-1873
	
		Journal Volume Volume 5
	
		Journal Issue Volume 5, Number 3 / September, 2007 (Source: Current Osteoporosis Reports)</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2371859</comments>
            <pubDate>Sun, 26 Apr 2009 05:56:15 +0100</pubDate>
            <guid isPermaLink="false">2371859</guid>        </item>
        <item>
            <title>Cancer-associated bone disease</title>
            <link>http://www.medworm.com/index.php?rid=2371858&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F8l6p78pu00087041%2F</link>
            <description>This article reviews risk factors and mechanisms associated with cancer-related
 bone loss and metastases as well as strategies for the detection of bone-related complications of cancer and therapies to
 treat these complications. This article focuses on the more common cancers with adverse skeletal effects: breast cancer, prostate
 cancer, and multiple myeloma.
 
	Content Type Journal ArticleDOI 10.1007/s11914-007-0027-8Authors
		Sue A. Brown, University of Virginia Department of Medicine P.O. Box 801420 Charlottesville VA 22908 USATheresa A. Guise
	

	
		Journal Current Osteoporosis ReportsOnline ISSN 1544-2241Print ISSN 1544-1873
	
		Journal Volume Volume 5
	
		Journal Issue Volume 5, Number 3 / September, 2007 (Source: Current Osteoporosis Reports)</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2371858</comments>
            <pubDate>Sun, 26 Apr 2009 05:56:15 +0100</pubDate>
            <guid isPermaLink="false">2371858</guid>        </item>
        <item>
            <title>Web alert</title>
            <link>http://www.medworm.com/index.php?rid=2371857&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq553308t29r7rt87%2F</link>
            <description>Content Type Journal ArticleDOI 10.1007/s11914-007-0022-0

	
		Journal Current Osteoporosis ReportsOnline ISSN 1544-2241Print ISSN 1544-1873
	
		Journal Volume Volume 5
	
		Journal Issue Volume 5, Number 3 / September, 2007 (Source: Current Osteoporosis Reports)</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2371857</comments>
            <pubDate>Sun, 26 Apr 2009 05:56:15 +0100</pubDate>
            <guid isPermaLink="false">2371857</guid>        </item>
        <item>
            <title>Osteogenesis imperfecta: Epidemiology and pathophysiology</title>
            <link>http://www.medworm.com/index.php?rid=2371856&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F918585t2235162h3%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Osteogenesis imperfecta (OI) is the most common of the inherited connective tissue disorders that primarily affect bone. However,
 it is a systemic disorder, as evidenced by the occurrence of ocular complications, dentinogenesis imperfecta, hearing loss,
 joint laxity, restrictive pulmonary disease, and short stature. The OI classification initially included four phenotypes (I–IV)
 involving COL1A1 and COL1A2 mutations. Three new phenotypes have been added, of which one, type VII, is the result of mutations of the cartilage-associated
 protein (CRTAP) gene. Investigation of recessive forms of OI particularly reported among South African blacks have revealed mutations involving
 both the CRTAP gene and the leucine proline-enriched proteoglycan 1 (LEPRE1) gene, each inv...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2371856</comments>
            <pubDate>Sun, 26 Apr 2009 05:56:15 +0100</pubDate>
            <guid isPermaLink="false">2371856</guid>        </item>
        <item>
            <title>Pediatric bone density and fracture</title>
            <link>http://www.medworm.com/index.php?rid=2371855&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh8j03228v7708230%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;As children grow, they accumulate bone mineral, which serves as a “bone bank” for the future. Any condition that interferes
 with normal bone mineral accrual during childhood has the potential to reduce peak bone mass and subsequently increase future
 risk for fracture. In contrast to adults, for whom dual-energy x-ray absorptiometry (DXA) has become the standard clinical
 instrument for assessing bone mineral density and criteria have been developed to define osteopenia and osteoporosis, information
 for children is still limited. Numerous issues confound the interpretation of DXA-derived bone mineral density measurements
 in children, and clinicians often find themselves caught between the limitations of these methods and the practical issue
 of taking care of the...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2371855</comments>
            <pubDate>Sun, 26 Apr 2009 05:56:15 +0100</pubDate>
            <guid isPermaLink="false">2371855</guid>        </item>
        <item>
            <title>Etidronate: What is its place in treatment of primary osteoporosis and other demineralizing diseases today?</title>
            <link>http://www.medworm.com/index.php?rid=2371862&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm7346248j38g0846%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Bisphosphonate drugs are the major treatment options for primary and secondary osteoporosis and other demineralizing bone
 diseases. This class of drugs was presaged over a decade ago when etidronate disodium, the “mother compound” for modern-day
 bisphosphonates, was first used in the treatment of osteoporosis. The cyclic use of etidronate in therapy, which is known
 mainly to specialists in the field, is not approved in the United States. The drug does, however, have a worldwide reputation
 as a relatively inexpensive, efficacious, and highly tolerable treatment for osteoporosis. Many studies still describe its
 use for primary osteoporosis and some have described use in immobilization bone loss, periprosthetic bone loss, and even glucocorticoid-induced
 osteoporo...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2371862</comments>
            <pubDate>Sun, 26 Apr 2009 05:56:07 +0100</pubDate>
            <guid isPermaLink="false">2371862</guid>        </item>
        <item>
            <title>Diabetes, fracture, and bone fragility</title>
            <link>http://www.medworm.com/index.php?rid=2371861&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw264j3m6w3525655%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Recent studies have added to the evidence that type 1 and type 2 diabetes are associated with increased risk of hip fracture
 and other fractures. More frequent falls probably account for some of this increased risk, but reduced bone strength may also
 play a role. Although type 1 diabetes is associated with lower bone density, those with type 2 diabetes usually have elevated
 bone density. Yet for both types of diabetes, bone appears to be more fragile for a given density. Diabetes can affect bone
 through multiple pathways—some with contradictory effects—including obesity, insulin levels, hyperglycemia, and advanced glycation
 end products in collagen. Treatment with thiazolidinediones may increase fracture risk, at least in older women. Clinicians
 need to be awa...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2371861</comments>
            <pubDate>Sun, 26 Apr 2009 05:56:07 +0100</pubDate>
            <guid isPermaLink="false">2371861</guid>        </item>
        <item>
            <title>Bone biopsy in patients with osteoporosis</title>
            <link>http://www.medworm.com/index.php?rid=2371864&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F5068325013g287x3%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Although rarely used to diagnose and manage patients with osteoporosis, bone biopsies are performed to establish bone quality,
 including degree of mineralization and microarchitecture; to assess bone turnover and bone loss mechanisms; and to analyze
 treatment effects on bone structure and bone turnover. Bone biopsies are also the only method to diagnose mineralization defect
 or frank osteomalacia. Due to the availability of antiresorptive agents and anabolic drugs, determining bone turnover and
 bone-loss mechanisms is critical to appropriate treatment regimen selection. Bone biopsies establish the safety and efficacy
 of new therapeutic modalities. Further, new techniques such as molecular morphometry (in situ hybridization and immunohistochemistry)
 and analysis of...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2371864</comments>
            <pubDate>Sun, 26 Apr 2009 05:56:06 +0100</pubDate>
            <guid isPermaLink="false">2371864</guid>        </item>
        <item>
            <title>Over-suppression of bone turnover: Does it exist?</title>
            <link>http://www.medworm.com/index.php?rid=2371863&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F59362j8515531611%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Bone-turnover suppression is central to the therapeutic benefit of many interventions used to prevent osteoporotic fractures.
 There are theoretical concerns that long-term suppression may have adverse effects on bone strength, although at present no
 direct evidence exists that this happens. Nevertheless, further research is required to establish the optimal duration of
 treatment with antiresorptive agents.
 
	Content Type Journal ArticleDOI 10.1007/s11914-007-0014-0Authors
		Juliet Compston, Addenbrooke’s Hospital Department of Medicine Box 157 Cambridge CB2 2QQ UK
	

	
		Journal Current Osteoporosis ReportsOnline ISSN 1544-2241Print ISSN 1544-1873
	
		Journal Volume Volume 5
	
		Journal Issue Volume 5, Number 4 / December, 2007 (Source: Current Osteoporosis Report...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2371863</comments>
            <pubDate>Sun, 26 Apr 2009 05:56:06 +0100</pubDate>
            <guid isPermaLink="false">2371863</guid>        </item>
        <item>
            <title>Anorexia, bulimia, and the athletic triad: Evaluation and management</title>
            <link>http://www.medworm.com/index.php?rid=2371866&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl23u22685762532r%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Caloric restriction caused by undernutrition or overexercise is increasingly common and has significant health consequences
 such as hypothalamic amenorrhea, infertility, attainment of low peak bone mass, and bone loss leading to fracture. In these
 patients, the pathophysiology of amenorrhea and bone loss is multifactorial, involving hormones that integrate the nutritional
 state with the hypothalamic-pituitary-ovarian axis, including leptin and possibly ghrelin. The pathophysiology of bone loss
 includes nutritional deficiencies, possibly estrogen deficiency, and direct and indirect effects of leptin on bone. Identifying
 patients at risk for low bone mineral density and fracture is important, as is screening with dual energy radiograph absorptiometry.
 Treatment has ...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2371866</comments>
            <pubDate>Sun, 26 Apr 2009 05:56:05 +0100</pubDate>
            <guid isPermaLink="false">2371866</guid>        </item>
        <item>
            <title>Bone loss in patients with breast or prostate cancer</title>
            <link>http://www.medworm.com/index.php?rid=2371865&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fvtp06158g6684345%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Cancers of the breast and prostate are very common in the general population, with breast cancer accounting worldwide for
 23% of cancer cases in women and prostate cancer accounting for 12% of cases in men. During the past decade, the survival
 rates of patients with estrogen-dependent breast cancer and testoster-one-dependent prostate cancer have improved. This improvement
 has been possible thanks to the introduction of hormone treatments that suppress the synthesis or antagonize the actions of
 gonadal steroids. However, estrogen and testosterone deficiencies are associated with excessive bone resorption that translates
 into damage of the bone microarchitecture, loss of bone mineral density, and predisposition to osteoporosis and fractures.
 Herein, we review the m...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2371865</comments>
            <pubDate>Sun, 26 Apr 2009 05:56:05 +0100</pubDate>
            <guid isPermaLink="false">2371865</guid>        </item>
        <item>
            <title>The role of hormone therapy and calcium plus vitamin D for reduction of bone loss and risk for fractures: Lessons learned from the women’s health initiative</title>
            <link>http://www.medworm.com/index.php?rid=2371868&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F47u566w5363w2246%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Osteoporosis, a major public health problem, is characterized by increased risk for fracture. To reduce the morbidity and
 excess loss of life associated with this common disease, we need to understand the efficacy of treatment strategies for fracture
 reduction. The Women’s Health Initiative Clinical Trials have extended our understanding of the effect of hormone therapy
 and calcium plus vitamin D supplements on risk for hip and total fractures. Although estrogen, with or without progestin,
 significantly decreases fracture risk at all skeletal sites—almost irrespective of underlying risk for osteoporosis—its risks
 outweigh its benefits, negating its general use for fracture reduction. For calcium-replete women, calcium plus vitamin D
 supplementation has a non...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2371868</comments>
            <pubDate>Sun, 26 Apr 2009 05:56:04 +0100</pubDate>
            <guid isPermaLink="false">2371868</guid>        </item>
        <item>
            <title>Medication-induced osteoporosis</title>
            <link>http://www.medworm.com/index.php?rid=2371867&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc73263m733837wx7%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Osteoporosis, a condition of low bone mass and microarchitectural deterioration, results in fractures with minimal trauma.
 Secondary osteoporosis is defined as bone loss resulting from either specific clinical disorders or medications. Some medications
 that can induce osteoporosis are discussed. Specifically, this article reviews the pathogenesis of glucocorticoid-induced
 bone loss and demonstrates the means to successfully manage the condition with a combination of calcium and vitamin D supplementation
 and, depending on the severity of the bone loss, bisphosphonates or parathyroid hormone. In addition, the pathphysiology of
 bone loss from aromatase inhibitors in women, gonadotropin-releasing hormone agonists in men, anticonvulsant medications,
 and proton pump inh...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2371867</comments>
            <pubDate>Sun, 26 Apr 2009 05:56:04 +0100</pubDate>
            <guid isPermaLink="false">2371867</guid>        </item>
        <item>
            <title>Web alert</title>
            <link>http://www.medworm.com/index.php?rid=2371869&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh4582m466u350176%2F</link>
            <description>Content Type Journal ArticleDOI 10.1007/s11914-007-0015-z

	
		Journal Current Osteoporosis ReportsOnline ISSN 1544-2241Print ISSN 1544-1873
	
		Journal Volume Volume 5
	
		Journal Issue Volume 5, Number 4 / December, 2007 (Source: Current Osteoporosis Reports)</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2371869</comments>
            <pubDate>Sun, 26 Apr 2009 05:55:59 +0100</pubDate>
            <guid isPermaLink="false">2371869</guid>        </item>
        <item>
            <title>Glucocorticoid-induced osteoporosis</title>
            <link>http://www.medworm.com/index.php?rid=2253285&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw62868391h443563%2F</link>
            <description>This article reviews current information
 on the epidemiology, pathophysiology, and clinical studies that support using bone-active agents to prevent and treat GIO.
 
	Content Type Journal ArticleDOI 10.1007/s11914-009-0005-4Authors
		Stuart L. Silverman, Cedars-Sinai/UCLA and OMC Clinical Research Center 8641 Wilshire Boulevard, Suite 301 Beverly Hills CA 90211 USANancy E. Lane
	

	
		Journal Current Osteoporosis ReportsOnline ISSN 1544-2241Print ISSN 1544-1873
	
		Journal Volume Volume 7
	
		Journal Issue Volume 7, Number 1 / March, 2009 (Source: Current Osteoporosis Reports)</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2253285</comments>
            <pubDate>Tue, 10 Mar 2009 08:12:16 +0100</pubDate>
            <guid isPermaLink="false">2253285</guid>        </item>
        <item>
            <title>Denosumab: Anti-RANKL antibody</title>
            <link>http://www.medworm.com/index.php?rid=2253287&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fdxxm083843n65026%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Denosumab (anti-receptor activator of nuclear factorκB ligand [RANKL] antibody) is a novel agent, a fully human monoclonal
 antibody that inhibits osteoclastic-medicated bone resorption by binding to osteoblast-produced RANKL. By reducing RANKL binding
 to the osteoclast receptor RANK, bone resorption and turnover decrease. In phase 2 dose-ranging studies, denosumab had a rapid
 onset and offset effect. Also, in patients who had received 2 years of denosumab and were discontinued for the third year,
 rechallenge with denosumab during the fourth year demonstrated a return of responsiveness to denosumab that mimicked the initial
 treatment. Phase 3 pivotal fracture data were recently presented with positive outcome data; denosumab (60 mg subcutaneously
 every 6 months) s...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2253287</comments>
            <pubDate>Tue, 10 Mar 2009 08:12:15 +0100</pubDate>
            <guid isPermaLink="false">2253287</guid>        </item>
        <item>
            <title>Bisphosphonates for postmenopausal osteoporosis: Determining duration of treatment</title>
            <link>http://www.medworm.com/index.php?rid=2253289&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl43gq71002936g81%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Doctors who treat patients with osteoporosis are increasingly confronted with the question of how long to continue treatment
 with bisphosphonates (BPs), which have the unique characteristic of accumulating in the skeleton. Limited available long-term
 data suggest that such decisions should be made on a case-by-case approach and guided by an individual re-evaluation of clinical
 fracture risks and bone mineral density, efficacy, and safety issues. In patients who still have a high fracture risk after
 5 years of treatment with BPs, continuing treatment could be considered, but stopping BPs could be appropriate in those with
 a low fracture risk after 5 years of treatment. Switching to recombinant human parathyroid hormone 1–34 or 1–84 is indicated
 when recurrent i...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2253289</comments>
            <pubDate>Tue, 10 Mar 2009 08:12:14 +0100</pubDate>
            <guid isPermaLink="false">2253289</guid>        </item>
        <item>
            <title>Nutritional therapies (including fosteum)</title>
            <link>http://www.medworm.com/index.php?rid=2253293&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu8213633h4726750%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Nutrition is important in promoting bone health and in managing an individual with low bone mass or osteoporosis. In adult
 women and men, known losses of bone mass and microarchitecture occur, and nutrition can help minimize these losses. In every
 patient, a healthy diet with adequate protein, fruits, vegetables, calcium, and vitamin D is required to maintain bone health.
 Recent reports on nutritional remedies for osteoporosis have highlighted the importance of calcium in youth and continued
 importance in conjunction with vitamin D as the population ages. It is likely that a calcium intake of 1200 mg/d is ideal,
 and there are some concerns about excessive calcium intakes. However, vitamin D intake needs to be increased in most populations.
 The ability of soy produ...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2253293</comments>
            <pubDate>Tue, 10 Mar 2009 08:12:13 +0100</pubDate>
            <guid isPermaLink="false">2253293</guid>        </item>
        <item>
            <title>Zoledronic acid reduces recurrent clinical fracture in patients with hip fracture</title>
            <link>http://www.medworm.com/index.php?rid=2253291&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F4428x63266701297%2F</link>
            <description>Content Type Journal ArticleCategory Clinical Trials ReportDOI 10.1007/s11914-009-0001-8Authors
		Stuart L. Silverman
	

	
		Journal Current Osteoporosis ReportsOnline ISSN 1544-2241Print ISSN 1544-1873
	
		Journal Volume Volume 7
	
		Journal Issue Volume 7, Number 1 / March, 2009 (Source: Current Osteoporosis Reports)</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2253291</comments>
            <pubDate>Tue, 10 Mar 2009 08:12:13 +0100</pubDate>
            <guid isPermaLink="false">2253291</guid>        </item>
        <item>
            <title>Quality health care gaps in osteoporosis: How can patients, providers, and the health system do a better job?</title>
            <link>http://www.medworm.com/index.php?rid=2253295&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa372g6628mk60854%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A significant gap exists between evidence-based advances and real-world clinical practice in the diagnosis and prevention
 of osteoporosis. The goal of osteoporosis care is to prevent fractures and improve health-related quality of life, and ideally
 lower mortality. Despite recent advances in osteoporosis detection and treatment options, studies suggest underdiagnosis and
 undertreatment of osteoporosis, even among those who have already sustained fractures. The challenges in translating knowledge
 into practice are multifaceted, with efforts directed at the patient, provider, and health care system levels achieving variable
 success at the population level. Methods to improve quality of care in osteoporosis need to be multipronged, with emphasis
 on clinical process i...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2253295</comments>
            <pubDate>Tue, 10 Mar 2009 08:12:10 +0100</pubDate>
            <guid isPermaLink="false">2253295</guid>        </item>
        <item>
            <title>Web alert</title>
            <link>http://www.medworm.com/index.php?rid=2183033&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fwv2kt22132835725%2F</link>
            <description>Content Type Journal ArticleDOI 10.1007/s11914-007-0001-5

	
		Journal Current Osteoporosis ReportsOnline ISSN 1544-2241Print ISSN 1544-1873
	
		Journal Volume Volume 5
	
		Journal Issue Volume 5, Number 2 / June, 2007 (Source: Current Osteoporosis Reports)</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2183033</comments>
            <pubDate>Wed, 11 Feb 2009 07:20:16 +0100</pubDate>
            <guid isPermaLink="false">2183033</guid>        </item>
        <item>
            <title>Novel osteoclast signaling mechanisms</title>
            <link>http://www.medworm.com/index.php?rid=2183032&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F6446n58560198h32%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Osteoclasts are cells of monocyte/macrophage origin that degrade bone matrix. Receptor activator of NF-κB ligand (RANKL) induces
 osteoclast differentiation in the presence of macrophage colony-stimulating factor. RANKL activates the tumor necrosis factor
 receptor-associated factor 6, c-Fos, and calcium signaling pathways, all of which are indispensable for the induction and
 activation of nuclear factor of activated T cells (NFAT) c1. NFATc1 is the master transcription factor for osteoclast differentiation,
 which regulates many osteoclast-specific genes. Multiple immunoglobulin-like receptors associated with immunoreceptor tyrosine-based
 activation motif (ITAM)-harboring adapters, Fc receptor common γ subunit (FcRγ), and DNAX-activating protein (DAP) 12 mediate
 ...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2183032</comments>
            <pubDate>Wed, 11 Feb 2009 07:20:16 +0100</pubDate>
            <guid isPermaLink="false">2183032</guid>        </item>
        <item>
            <title>Wnt signaling and the regulation of bone mass</title>
            <link>http://www.medworm.com/index.php?rid=2183031&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn827238101112q04%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Human genetic studies have firmly established a link between bone mass in humans and gain-of-function or loss-of-function
 mutations in a Wnt coreceptor, low-density lipoprotein receptor-related protein 5 (LRP5), or in the Wnt antagonist sclerostin,
 and several molecular genetic studies in mice have consistently confirmed the critical importance of the Wnt signaling pathway
 in skeletal biology and disease. In what may be a novel paradigm, the ubiquitous nature of LRP5/6 and Wnt signaling is counterbalanced
 by the bone-restricted and regulated expression of Wnt antagonists such as sclerostin and Dickkopf-1 (Dkk1) in adult tissues,
 offering new and potentially safe therapeutic means of intervention to stimulate bone formation.
 
	Content Type Journal ArticleDOI 10.100...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2183031</comments>
            <pubDate>Wed, 11 Feb 2009 07:20:16 +0100</pubDate>
            <guid isPermaLink="false">2183031</guid>        </item>
        <item>
            <title>The role of the collagen matrix in skeletal fragility</title>
            <link>http://www.medworm.com/index.php?rid=2183034&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F52g43380007wm22h%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The collagen network in bone provides resistance against fracture and may be susceptible to changes with aging and disease.
 This review identifies the changes in quality of collagen matrix as contributors to bone fragility. With aging and in diabetes,
 cross-links accumulate in bone collagen as a result of nonenzymatic glycation and consequently impair matrix properties, increasing
 bone fragility. Cell-culture and animal studies suggest that the accumulation of cross-links induced by nonenzymatic glycation
 may be related to a reduction in bone turnover resulting from the altered responses of osteoblasts and osteoclasts to advanced
 glycation end products.
 
	Content Type Journal ArticleDOI 10.1007/s11914-007-0004-2Authors
		Deepak Vashishth, Rensselaer Polytechnic In...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2183034</comments>
            <pubDate>Wed, 11 Feb 2009 07:20:14 +0100</pubDate>
            <guid isPermaLink="false">2183034</guid>        </item>
        <item>
            <title>Effects of microarchitecture on bone strength</title>
            <link>http://www.medworm.com/index.php?rid=2183036&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk5055k50p7724382%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Bone strength and stiffness depend strongly on bone mass, but they also depend on the microarchitecture and tissue quality
 of both cancellous and cortical bone. All these aspects differ between individuals and between anatomic sites. This review
 discusses ways to characterize the three-dimensional cancellous architecture as well as changes in architecture and bone composition
 caused by bone remodeling. The methods used range from detailed descriptions of sizes and distances in cancellous bone to
 coarser texture analysis methods using clinical data. As the resolution of clinical images increases, it may become possible
 to use knowledge of the relationship between bone microarchitecture and strength to predict fracture risk clinically.
 
	Content Type Journal Article...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2183036</comments>
            <pubDate>Wed, 11 Feb 2009 07:20:11 +0100</pubDate>
            <guid isPermaLink="false">2183036</guid>        </item>
        <item>
            <title>The biology of osteocytes</title>
            <link>http://www.medworm.com/index.php?rid=2183035&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F452x861r74gv6081%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Osteocytes, the most abundant cell type in bone, remain the least characterized. Several theories have been proposed regarding
 their function, including osteolysis, sensing the strains produced in response to mechanical loading of bones, and producing
 signals that affect the function of osteoblasts and osteoclasts and hence, bone turnover. This review also discusses the role
 of osteocyte apoptosis in targeted bone remodeling and proposes that the occurrence of osteocyte apoptosis is consistent with
 the description of apoptosis as an essential homeostatic mechanism for the healthy maintenance of tissues.
 
	Content Type Journal ArticleDOI 10.1007/s11914-007-0007-zAuthors
		Giolanta KogianniBrendon S. Noble, University of Edinburgh Medical School Musculoskeletal Tissu...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2183035</comments>
            <pubDate>Wed, 11 Feb 2009 07:20:11 +0100</pubDate>
            <guid isPermaLink="false">2183035</guid>        </item>
        <item>
            <title>Extending DXA beyond bone mineral density: Understanding hip structure analysis</title>
            <link>http://www.medworm.com/index.php?rid=2183037&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F21251208547m4p82%2F</link>
            <description>This article reviews the factors that govern the strength of an object, how they are used in
 engineering simulations, and how those properties can be extracted from DXA data. It is important to recognize that that although
 DXA scanners can be used to measure geometric strength, they were not designed to do so. The current HSA method is fundamentally
 limited to evaluating bending strength in the plane of the image, so precision is sensitive to consistent femur positioning.
 The positioning issue and other limitations of the HSA method are discussed, as well as the critical importance of body-size
 scaling when interpreting bone geometry. Also discussed is how current HSA limitations could be ameliorated in a “next-generation”
 DXA scanner that is optimized for the purpose.
 
	Content...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2183037</comments>
            <pubDate>Wed, 11 Feb 2009 07:20:10 +0100</pubDate>
            <guid isPermaLink="false">2183037</guid>        </item>
        <item>
            <title>Paget’s disease: Epidemiology and pathophysiology</title>
            <link>http://www.medworm.com/index.php?rid=1996734&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F415175346651n1h8%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Paget’s disease of bone is a focal disorder of aging bone. The classic late-onset Paget’s disease is often caused by a P392L
 mutation in the gene SQSTM1, which disturbs signaling pathways in osteoclasts on cell activation. This prevalent mutation is neither necessary nor sufficient
 to cause Paget’s disease. Its identification, along with the elucidation of other mutations underlying early-onset Paget’s
 and Paget’s disease seen in association with inclusion body myopathy and frontotemporal dementia, have redefined our understanding
 of genetic disorders of bone remodeling by emphasizing the importance of environmental determinants in their pathophysiology.
 
	Content Type Journal ArticleDOI 10.1007/s11914-008-0022-8Authors
		Margaret Seton, Massachusetts Gen...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1996734</comments>
            <pubDate>Thu, 27 Nov 2008 09:16:24 +0100</pubDate>
            <guid isPermaLink="false">1996734</guid>        </item>
        <item>
            <title>The skeleton: Endocrine regulator of phosphate homeostasis</title>
            <link>http://www.medworm.com/index.php?rid=1996733&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv7t33m2102625075%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Phosphorus is an essential element in skeletal development, bone mineralization, membrane composition, nucleotide structure,
 and cellular signaling. Phosphate, the principal form in which phosphorus is found in the body, is regulated by the complex
 interplay of the hormones parathyroid hormone (PTH), calcitriol (1,25[OH]2 vitamin D3), and fibroblast growth factor 23 (FGF23). These collectively govern bone mineralization, absorption of phosphorus by the
 intestine, and renal tubular reabsorption of phosphate. The skeleton is the major storage pool for phosphate and the principal
 production site for FGF23, a major phosphate regulatory hormone. Recent advances in understanding the molecular basis of disorders
 of phosphate metabolism have revealed new phosphate-regulato...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1996733</comments>
            <pubDate>Thu, 27 Nov 2008 09:16:24 +0100</pubDate>
            <guid isPermaLink="false">1996733</guid>        </item>
        <item>
            <title>Targeting the Wnt signaling pathway to augment bone formation</title>
            <link>http://www.medworm.com/index.php?rid=1996737&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F3731458212h81m07%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Recent discoveries in humans and mice have revealed that the Wnt (Wingless and Int-1) signaling pathway is responsible for
 a complex array of functions in maintaining bone homeostasis. The Wnt proteins are key modulators of mesenchymal lineage specification
 and regulate most aspects of osteoblast physiology and postnatal bone acquisition by controlling the differentiation and activity
 of osteoblasts and osteoclasts. Initial reports have indicated that activators of Wnt signaling are potent promoters of osteogenesis;
 however, systemic hyperactivation of the canonical Wnt pathway could potentially accelerate neoplastic transformation and
 subsequent tumor growth. Alternatively, recent investigations of natural soluble antagonists of Wnt signaling in bone suggest
 the ...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1996737</comments>
            <pubDate>Thu, 27 Nov 2008 09:16:23 +0100</pubDate>
            <guid isPermaLink="false">1996737</guid>        </item>
        <item>
            <title>Osteomalacia</title>
            <link>http://www.medworm.com/index.php?rid=1996736&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb2n1m63011031785%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The finding of low bone mineral density with a T-score of −2.5 or below on dual energy x-ray absorptiometry is usually reported
 as indicating that the patient has “osteoporosis” according to the World Health Organization classification, and, in postmenopausal
 women, it is often assumed that this is due to estrogen deficiency. However, up to one third of postmenopausal women have
 a secondary cause of low density, including osteomalacia. Osteomalacia is defined as a mineralization defect caused by disorders
 that lead to decreased mineralization of bone. Clues from the history, physical examination, laboratory tests, and radiographs
 may indicate that the patient suffers from a form of osteomalacia rather than postmenopausal estrogen deficiency alone. Establishin...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1996736</comments>
            <pubDate>Thu, 27 Nov 2008 09:16:23 +0100</pubDate>
            <guid isPermaLink="false">1996736</guid>        </item>
        <item>
            <title>Web alert</title>
            <link>http://www.medworm.com/index.php?rid=1996735&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fkv0733m71462uq12%2F</link>
            <description>Content Type Journal ArticleDOI 10.1007/s11914-008-0021-9

	
		Journal Current Osteoporosis ReportsOnline ISSN 1544-2241Print ISSN 1544-1873
	
		Journal Volume Volume 6
	
		Journal Issue Volume 6, Number 4 / December, 2008 (Source: Current Osteoporosis Reports)</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1996735</comments>
            <pubDate>Thu, 27 Nov 2008 09:16:23 +0100</pubDate>
            <guid isPermaLink="false">1996735</guid>        </item>
        <item>
            <title>Falls: Epidemiology, pathophysiology, and relationship to fracture</title>
            <link>http://www.medworm.com/index.php?rid=1996738&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ft4464883n101rk42%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Falls are common in the elderly, and frequently result in injury and disability. Most falls result from an interaction between
 individual characteristics that increase an individual’s propensity to fall and acute mediating risk factors that provide
 the opportunity to fall. Predisposing risk factors include age-associated changes in strength and balance, comorbidities such
 as osteoarthritis, visual impairment and dementia, psychotropic medications, and certain types of footwear. Fewer studies
 have focused on acute precipitating factors, but environmental and situational factors are clearly important to fall risk.
 Approximately 30% of falls result in an injury that requires medical attention, with fractures occurring in approximately
 10%. In addition to the risk f...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1996738</comments>
            <pubDate>Thu, 27 Nov 2008 09:16:22 +0100</pubDate>
            <guid isPermaLink="false">1996738</guid>        </item>
        <item>
            <title>Epidemiology of fracture risk in the Women’s Health Initiative</title>
            <link>http://www.medworm.com/index.php?rid=1996739&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa53244q6l755h13g%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Osteoporosis is one of the most disabling consequences of aging in women. Strategies that permit earlier identification of
 women at risk for fracture are needed. The Women’s Health Initiative has extended our knowledge of clinical risk factors and
 biomarkers of fracture risk in postmenopausal women. Based upon 11 clinically available risk factors (age, race/ethnicity,
 self-reported health, weight, height, physical activity, parental hip fracture, fracture history after age 54, current smoking,
 corticosteroid use, and history of treated diabetes), an algorithm has been developed to predict 5-year hip fracture risk.
 Biomarkers including low vitamin D or bioavailable testosterone and/or high cystatin C or sex hormone-binding globulin also
 predict risk for hip fract...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1996739</comments>
            <pubDate>Thu, 27 Nov 2008 09:16:20 +0100</pubDate>
            <guid isPermaLink="false">1996739</guid>        </item>
        <item>
            <title>Osteoporotic fractures: A brain or bone disease?</title>
            <link>http://www.medworm.com/index.php?rid=1901929&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe60thp6q3024886n%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Osteoporosis is a skeletal disorder that predisposes individuals to increased risk of fracture. However, most osteoporotic
 fractures occur in women who do not meet criteria for osteoporosis. Hence, bone density, by itself, is a relatively poor predictor
 of fracture. Age and age-related factors are now recognized as increasingly important in determining fracture risk. Osteoporotic
 fractures are associated with increased disability and mortality, suggesting that osteoporosis may be a clinical manifestation
 of an underlying disease process affecting multiple systems. The systems affected, the musculoskeletal system and the central
 nervous system, are shared in many respects with the frailty syndrome. Vitamin D deficiency is a major contributor to the
 frailty syndrome...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1901929</comments>
            <pubDate>Tue, 21 Oct 2008 05:44:12 +0100</pubDate>
            <guid isPermaLink="false">1901929</guid>        </item>
        <item>
            <title>Inhibin and the regulation of bone mass</title>
            <link>http://www.medworm.com/index.php?rid=1901931&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F53365l2rxn750736%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Inhibins A and B are gonadal peptide members of the transforming growth factor-β superfamily that serve as negative feedback
 regulators of pituitary follicle-stimulating hormone (FSH). Accumulating evidence suggests that bone turnover and bone loss
 increase in women before menopause and the decrease in serum estradiol levels. Increased FSH levels have been correlated with
 some of these perimenopausal changes, whereas decreased inhibins strongly correlate with increases in bone formation and resorption
 across the menopause transition, and predict lumbar bone mass in perimenopausal women, likely resulting from the direct inhibin
 suppression of osteoblast and osteoclast development. Interestingly, continuous exposure of mice to inhibin A in vivo is anabolic
 and prot...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1901931</comments>
            <pubDate>Tue, 21 Oct 2008 05:44:10 +0100</pubDate>
            <guid isPermaLink="false">1901931</guid>        </item>
        <item>
            <title>Web alert</title>
            <link>http://www.medworm.com/index.php?rid=1901930&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fd352274802558618%2F</link>
            <description>Content Type Journal ArticleDOI 10.1007/s11914-008-0008-6

	
		Journal Current Osteoporosis ReportsOnline ISSN 1544-2241Print ISSN 1544-1873
	
		Journal Volume Volume 6
	
		Journal Issue Volume 6, Number 2 / June, 2008 (Source: Current Osteoporosis Reports)</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1901930</comments>
            <pubDate>Tue, 21 Oct 2008 05:44:10 +0100</pubDate>
            <guid isPermaLink="false">1901930</guid>        </item>
        <item>
            <title>The osteogenic-angiogenic interface: Novel insights into the biology of bone formation and fracture repair</title>
            <link>http://www.medworm.com/index.php?rid=1901933&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F4689wu55k370018h%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;
 Bone never forms without vascular interactions. Although this is a very simple and obvious statement, the biological, clinical, and pharmacologic implications are incompletely
 appreciated. The vasculature is not only the conduit for nutrient-metabolite exchange and the rate-limiting “point-of-reference”
 for Haversian bone formation, but also provides the sustentacular niche for the self-renewing osteoprogenitor. This past year,
 significant advances have been made in our understanding of the osteogenic-angiogenic interface that are immediately germane
 to osteoporosis disease biology and fracture management. The critical contributions of the osteoblast oxygen-sensing machinery,
 paracrine vascular endothelial growth factor and placental growth factor signaling, ...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1901933</comments>
            <pubDate>Tue, 21 Oct 2008 05:44:09 +0100</pubDate>
            <guid isPermaLink="false">1901933</guid>        </item>
        <item>
            <title>Leptin as an endocrine signal in bone</title>
            <link>http://www.medworm.com/index.php?rid=1901932&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fcj31317hk2730507%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Leptin and its actions in bone came to prominence in 2000, with the publication of two landmark articles identifying a novel
 interaction between energy and bone homeostasis, as well as a novel hypothalamic circuit to the skeleton. However, they also
 revealed the dichotomous nature of leptin’s effect on the skeleton. Subsequent research has increased understanding of the
 factors critical to interpretation of the leptin-bone signaling. These include opposing effects in cortical and cancellous
 bone, central and peripheral effects, involvement of other neural and endocrine factors, and leptin receptor polymorphisms
 in human populations. It is clear that leptin can markedly influence the regulation of bone mass, and that study of this pathway
 continues to increase ou...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1901932</comments>
            <pubDate>Tue, 21 Oct 2008 05:44:09 +0100</pubDate>
            <guid isPermaLink="false">1901932</guid>        </item>
        <item>
            <title>Parathyroid hormone and the cardiovascular system</title>
            <link>http://www.medworm.com/index.php?rid=1901935&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F3434243p2079574x%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The classical actions of parathyroid hormone (PTH) are well recognized, but its effects on other target tissues, such as the
 cardiovascular system, are less appreciated. Several studies have evaluated the effects of PTH in patients with primary hyperparathyroidism
 in order to understand potential cardiovascular effects in terms of hypertension, cardiovascular mortality, left ventricular
 function, and endothelial function. We review these studies and evaluate the cellular mechanisms that may affect these outcomes.
 
	Content Type Journal ArticleDOI 10.1007/s11914-008-0014-8Authors
		Lorraine A. Fitzpatrick, Musculoskeletal Diseases, GlaxoSmithKline Research and Development 2301 Renaissance Boulevard, RN0420 King of Prussia PA 19406 USAJohn P. BilezikianShonni J. Silve...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1901935</comments>
            <pubDate>Tue, 21 Oct 2008 05:44:08 +0100</pubDate>
            <guid isPermaLink="false">1901935</guid>        </item>
        <item>
            <title>The cell biology of parathyroid hormone in osteoblasts</title>
            <link>http://www.medworm.com/index.php?rid=1901934&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fbl14874332405212%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Continuous exposure to parathyroid hormone (PTH) is associated with catabolic effects, whereas intermittent exposure to low
 doses of PTH is associated with anabolic effects. By controlling osteoblast function, PTH increases bone formation on cancellous,
 endocortical, and periosteal bone surfaces. In general, PTH does not affect the replication of uncommitted osteoblast progenitors
 but suppresses proliferation of committed osteoprogenitors. Intermittent PTH promotes osteoblast differentiation, in part,
 by its ability to promote exit from the cell cycle, to activate Wnt signaling in osteoblasts, and to inhibit the Wnt antagonist
 sclerostin in osteocytes. Insulin-like growth factor-1 is also required for the actions of PTH to increase osteoblast numbers.
 Intermittent...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1901934</comments>
            <pubDate>Tue, 21 Oct 2008 05:44:08 +0100</pubDate>
            <guid isPermaLink="false">1901934</guid>        </item>
        <item>
            <title>Vertebroplasty and kyphoplasty update</title>
            <link>http://www.medworm.com/index.php?rid=1895550&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe02g88138119j824%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Vertebroplasty and kyphoplasty are minimally invasive vertebral augmentation procedures in which a filler material is percutaneously
 injected into a vertebral body for the treatment of vertebral fractures associated with osteoporosis, malignant conditions,
 hemangiomas, and osteonecrosis. In vertebroplasty, the filler is injected directly into the bone, whereas in kyphoplasty,
 the filler is injected into a cavity created by inflation of a balloon tamp. The goals of treatment include pain relief, fracture
 stabilization, restoration of vertebral height, and strengthening of the vertebral body to reduce the risk of a future fracture
 at the same level. When performed by a well-trained physician in appropriately selected patients, vertebral augmentation is
 usually effec...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1895550</comments>
            <pubDate>Sat, 18 Oct 2008 11:08:32 +0100</pubDate>
            <guid isPermaLink="false">1895550</guid>        </item>
        <item>
            <title>Nonvertebral fracture risk reduction with nitrogen-containing bisphosphonates</title>
            <link>http://www.medworm.com/index.php?rid=1895549&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx866660222312153%2F</link>
            <description>This article summarizes the most currently available
 data relative to nonvertebral and hip fracture risk reduction for the N-containing bisphosphonates alendronate, ibandronate,
 risedronate, and zoledronic acid, and presents results of an analysis of comparative efficacy of these compounds using the
 technique of adjusted indirect comparisons.
 
	Content Type Journal ArticleDOI 10.1007/s11914-008-0016-6Authors
		Marc C. Hochberg, University of Maryland School of Medicine 10 South Pine Street, MSTF 8-34 Baltimore MD 21201 USA
	

	
		Journal Current Osteoporosis ReportsOnline ISSN 1544-2241Print ISSN 1544-1873
	
		Journal Volume Volume 6
	
		Journal Issue Volume 6, Number 3 / September, 2008 (Source: Current Osteoporosis Reports)</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1895549</comments>
            <pubDate>Sat, 18 Oct 2008 11:08:32 +0100</pubDate>
            <guid isPermaLink="false">1895549</guid>        </item>
        <item>
            <title>New thoughts about estrogen therapy from the Women’s Health Initiative</title>
            <link>http://www.medworm.com/index.php?rid=1895548&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx7n0776kx5r31750%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Since the introduction of hormone replacement therapy (HRT) in 1942, the availability of scientific information regarding
 the physiologic action of estrogen alone and in combination with progesterone has grown substantially. The specific physiology
 of changes in endogenous estrogen as a causal factor in bone loss that occurs as the result of menopause is now better understood.
 Accumulating evidence regarding the benefit of estrogen in protecting against bone loss at the time of menopause made it the
 first choice for prevention and treatment of osteoporosis, until the findings of the Women’s Health Initiative (WHI) were
 announced in 2002. Fortunately, the availability of multiple alternative agents for prevention and treatment of osteoporosis
 in menopausal women ...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1895548</comments>
            <pubDate>Sat, 18 Oct 2008 11:08:32 +0100</pubDate>
            <guid isPermaLink="false">1895548</guid>        </item>
        <item>
            <title>Evaluation and correction of low vitamin D status</title>
            <link>http://www.medworm.com/index.php?rid=1895547&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fyu455081334jw067%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Low vitamin D status, which is endemic due to inadequate oral intake combined with sun avoidance, contributes to musculoskeletal
 and other pathologies. Although controversial, it is increasingly recommended that serum 25-hydroxyvitamin D (25[OH]D) concentrations
 less than 30 ng/mL be considered suboptimal. Clinicians should appreciate that 25(OH)D measurements, like all quantitative
 laboratory tests, are subject to assay and biologic variability. Additionally, international standardized calibrators do not
 exist for 25(OH)D measurement. As such, a single 25(OH)D value of “30 ng/mL” may have substantial variability surrounding
 it, thereby making 25(OH)D levels of approximately 35 to 40 ng/mL a reasonable therapeutic goal to assure vitamin D adequacy.
 Achieving s...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1895547</comments>
            <pubDate>Sat, 18 Oct 2008 11:08:32 +0100</pubDate>
            <guid isPermaLink="false">1895547</guid>        </item>
        <item>
            <title>Management of osteoporosis in geriatric populations</title>
            <link>http://www.medworm.com/index.php?rid=1895546&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F82u172031r74145k%2F</link>
            <description>This article reviews recent research findings of general measures and pharmacologic therapy
 that are applicable to managing osteoporosis in the elderly.
 
	Content Type Journal ArticleDOI 10.1007/s11914-008-0018-4Authors
		Diane L. Schneider, University of California San Diego, La Jolla CA 92093 USA
	

	
		Journal Current Osteoporosis ReportsOnline ISSN 1544-2241Print ISSN 1544-1873
	
		Journal Volume Volume 6
	
		Journal Issue Volume 6, Number 3 / September, 2008 (Source: Current Osteoporosis Reports)</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1895546</comments>
            <pubDate>Sat, 18 Oct 2008 11:08:32 +0100</pubDate>
            <guid isPermaLink="false">1895546</guid>        </item>
        <item>
            <title>Web alert</title>
            <link>http://www.medworm.com/index.php?rid=1895545&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F8r382775705764x6%2F</link>
            <description>Content Type Journal ArticleDOI 10.1007/s11914-008-0015-7

	
		Journal Current Osteoporosis ReportsOnline ISSN 1544-2241Print ISSN 1544-1873
	
		Journal Volume Volume 6
	
		Journal Issue Volume 6, Number 3 / September, 2008 (Source: Current Osteoporosis Reports)</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1895545</comments>
            <pubDate>Sat, 18 Oct 2008 11:08:32 +0100</pubDate>
            <guid isPermaLink="false">1895545</guid>        </item>
        <item>
            <title>Osteoporosis in Men: Pathophysiology and treatment</title>
            <link>http://www.medworm.com/index.php?rid=1720534&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb487778t67032537%2F</link>
            <description>This article reviews what is known
 about the factors in men that lead to acquisition, maintenance, and loss of bone, as well as new insights into causes, pathogenesis,
 and treatment of osteoporosis in men.
 
	Content Type Journal ArticleCategory TherapeuticsDOI 10.1007/BF02938619Authors
		Luigi GennariJohn P. Bilezikian, College of Physicians and Surgeons 630 W. 168th Street 10032 New York NY USA
	

	
		Journal Current Osteoporosis ReportsOnline ISSN 1544-2241Print ISSN 1544-1873
	
		Journal Volume Volume 5
	
		Journal Issue Volume 5, Number 1 / March, 2007 (Source: Current Osteoporosis Reports)</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1720534</comments>
            <pubDate>Tue, 19 Aug 2008 17:21:45 +0100</pubDate>
            <guid isPermaLink="false">1720534</guid>        </item>
        <item>
            <title>Do estrogen or selective estrogen receptor modulators improve quality of life for women with postmenopausal osteoporosis?</title>
            <link>http://www.medworm.com/index.php?rid=1720536&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F26267810x0x05tnt%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Osteoporotic fractures result in significant deficits in health-related quality of life (HRQOL). The accumulation of deficits
 resulting from osteoporosis and fractures is now recognized as a major cause of reduced HRQOL in women after the menopause
 and in later life. Some of these same postmenopausal women may also have deficits in HRQOL related to vasomotor symptoms during
 the menopausal transition. Although estrogen therapy has not been shown to improve overall HRQOL in late postmenopausal women
 in randomized, controlled trials, it may improve menopausal symptoms. In contrast, selective estrogen receptor modulators
 (SERMs) such as raloxifene may increase vasomotor symptoms. Although estrogen is not indicated for the primary prevention
 of osteoporosis, estrogen t...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1720536</comments>
            <pubDate>Tue, 19 Aug 2008 17:21:42 +0100</pubDate>
            <guid isPermaLink="false">1720536</guid>        </item>
        <item>
            <title>Use of intravenous bisphosphonates in osteoporosis</title>
            <link>http://www.medworm.com/index.php?rid=1720535&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj46xq2771860t405%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Bisphosphonates, which are potent bone resorption inhibitors, currently are the mainstay of treatment for osteoporosis. Antifracture
 efficacy has been demonstrated for at least three nitrogen-containing bisphosphonates in oral formulations that are designed
 to be administered in weekly or monthly dosing regimens. Frequent reports of adverse events, primarily related to the upper
 gastrointestinal tract, and the strict dosing schedule necessary for oral bisphosphonate therapy are considered the major
 reasons for disappointing adherence to therapy. New intravenous formulations have been developed that allow dosing at very
 long intervals, thus avoiding the gastrointestinal complications associated with oral bisphosphonates and, it is hoped, improving
 compliance, parti...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1720535</comments>
            <pubDate>Tue, 19 Aug 2008 17:21:42 +0100</pubDate>
            <guid isPermaLink="false">1720535</guid>        </item>
        <item>
            <title>Monitoring osteoporosis therapies</title>
            <link>http://www.medworm.com/index.php?rid=1720539&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq361377223250h38%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Postmenopausal osteoporosis (PMO) is a progressive disease of bone loss, fractures, or both. The progression of osteoporosis
 leads to increased mortality and morbidity and impairs quality of life. There are effective treatments that prevent bone loss,
 increase bone strength, and reduce fracture risk. Improvement in persistence and adherence to therapy leads to better clinical
 outcomes. The management of PMO is facilitated by measuring surrogate markers of the efficacy of PMO treatments: 1) bone mineral
 density, 2) bone turnover markers, and 3) assessment of spinal integrity by vertebral fracture assessment by dual-energy x-ray
 absorptiometry. Appropriate use of markers measures the patient’s baseline fracture risk and monitors response to treatments.
 Clinicians ...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1720539</comments>
            <pubDate>Tue, 19 Aug 2008 17:21:41 +0100</pubDate>
            <guid isPermaLink="false">1720539</guid>        </item>
        <item>
            <title>Transplantation osteoporosis</title>
            <link>http://www.medworm.com/index.php?rid=1720538&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F10068362j6x6g004%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Transplantation is an established therapy for end-stage diseases of the kidney, endocrine pancreas, heart, liver, and lung,
 and for many hematologic disorders. Improved survival rates have been accompanied by increased recognition of previously neglected
 longterm complications of transplantation such as fractures and osteoporosis. Pretransplantation bone disease and immunosuppressive
 therapy result in rapid bone loss and increased fracture rates early after transplantation. Patients should be assessed and
 pretransplantation bone disease should be treated. Preventive therapy initiated in the immediate posttransplantation period
 is indicated in patients with osteopenia or osteoporosis, as further bone loss will occur in the first several months after
 transplantation...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1720538</comments>
            <pubDate>Tue, 19 Aug 2008 17:21:41 +0100</pubDate>
            <guid isPermaLink="false">1720538</guid>        </item>
        <item>
            <title>Prevention and treatment of glucocorticoid-induced osteoporosis</title>
            <link>http://www.medworm.com/index.php?rid=1720537&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F980q387745055437%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Glucocorticoids continue to be used for many inflammatory diseases, and glucocorticoid-induced osteoporosis (GIOP) remains
 the most common secondary form of metabolic bone disease. Recent meta-analyses suggest that both active and native vitamin
 D can help maintain lumbar spine bone mineral density (BMD), particularly in patients receiving lower-dose glucocorticoid
 therapy. Recent randomized, controlled clinical trials have shown that oral bisphosphonates are superior to vitamin D in maintaining
 BMD and should be continued for as long as a person receives glucocorticoid treatment. Similar to the oral bisphosphonates,
 intravenous ibandronate has been shown to preserve BMD and also to significantly reduce vertebral fracture risk. Increasing
 evidence supports a role ...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1720537</comments>
            <pubDate>Tue, 19 Aug 2008 17:21:41 +0100</pubDate>
            <guid isPermaLink="false">1720537</guid>        </item>
        <item>
            <title>Vitamin D therapy</title>
            <link>http://www.medworm.com/index.php?rid=1340892&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu3072p7u17q66235%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The fat-soluble vitamin D prohormones, ergocalciferol (vitamin D2) and cholecalciferol (vitamin D3), are essential for the efficient intestinal absorption of calcium and phosphate and the subsequent mineralization of bone.
 Inadequate vitamin D leads to chronic secondary hyperparathyroidism and osteoporosis. The increasing prevalence of osteoporosis
 has paralleled a pandemic of vitamin D insufficiency. Based on observational and prospective trials with clinical end points,
 the standards for vitamin D sufficiency have been recently revised. All patients with osteopenia or osteoporosis should be
 monitored with a reliable assay to maintain serum 25-hydroxyvitamin D levels more than 32 ng/dL. Patients who are taking bisphosphonates
 and those with coexisting primary hype...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1340892</comments>
            <pubDate>Sat, 29 Mar 2008 09:11:42 +0100</pubDate>
            <guid isPermaLink="false">1340892</guid>        </item>
        <item>
            <title>Web alert</title>
            <link>http://www.medworm.com/index.php?rid=1340891&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F47146x7l73637432%2F</link>
            <description>Content Type Journal ArticleDOI 10.1007/s11914-008-0001-0

	
		Journal Current Osteoporosis ReportsOnline ISSN 1544-2241Print ISSN 1544-1873
	
		Journal Volume Volume 6
	
		Journal Issue Volume 6, Number 1 / March, 2008 (Source: Current Osteoporosis Reports)</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1340891</comments>
            <pubDate>Sat, 29 Mar 2008 09:11:42 +0100</pubDate>
            <guid isPermaLink="false">1340891</guid>        </item>
        <item>
            <title>Osteonecrosis of the jaws and bisphosphonates</title>
            <link>http://www.medworm.com/index.php?rid=1340890&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc481127u521p0324%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Osteonecrosis of the jaws associated with bisphosphonate therapy was first identified in 2003 as a condition typified by exposed
 bone that does not heal after 8 weeks. Other signs and symptoms, such as pain and infection, may or may not be present. There
 is a strong need for consensus on a case definition for this condition. This condition has occurred primarily among cancer
 patients treated with the aminobisphosphonates zoledronic acid and pamidronate. The etiology of this condition remains unknown;
 however, oral disease and trauma appear to be important risk factors. This condition appears to be rare in metabolic bone
 disease and Paget’s disease, with an estimated prevalence of approximately 1 per 100,000 person-years. Thus, the benefits
 of bisphosphonate ther...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1340890</comments>
            <pubDate>Sat, 29 Mar 2008 09:11:42 +0100</pubDate>
            <guid isPermaLink="false">1340890</guid>        </item>
        <item>
            <title>Intravenous zoledronic acid for the treatment of osteoporosis</title>
            <link>http://www.medworm.com/index.php?rid=1340894&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb536p46p448184r5%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Osteoporosis is a preventable disease characterized by loss of bone mineral density, progression to diminished skeletal integrity,
 extensive bone fragility, and an increased risk of fracture. Morbidity and mortality from osteoporosis are significant, and
 the public health costs are substantial. Although safe and effective therapy is available, the disease remains underdiagnosed
 and undertreated. Oral bisphosphonates such as alendronate, risedronate, and ibandronate are the current first-line therapy;
 however, adherence to treatment is suboptimal, largely because the treatment regimen is difficult to follow. The bisphosphonate
 zoledronic acid (zoledronate), 5 mg, is administered as an annual 15-minute intravenous infusion for the treatment of postmenopausal
 osteopo...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1340894</comments>
            <pubDate>Sat, 29 Mar 2008 09:11:41 +0100</pubDate>
            <guid isPermaLink="false">1340894</guid>        </item>
        <item>
            <title>Combination anabolic and antiresorptive therapy for osteoporosis: Opening the anabolic window</title>
            <link>http://www.medworm.com/index.php?rid=1340893&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk004527136223646%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Antiresorptive agents for osteoporosis are a cornerstone of therapy, but anabolic drugs have recently increased our options.
 By stimulating bone formation, anabolic agents reduce fracture incidence by improving bone qualities in addition to increasing
 bone mass. The only anabolic agent currently approved for osteoporosis by the US Food and Drug Administration, teriparatide
 (recombinant human parathyroid hormone [1–34]), has emerged as a major approach to selected patients with osteoporosis. Recombinant
 human parathyroid hormone (1–84) is also available in Europe. Teriparatide increases bone density and bone turnover, improves
 microarchitecture, and changes bone size. The incidence of vertebral and nonvertebral fractures is reduced. A current concept
 in the mec...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1340893</comments>
            <pubDate>Sat, 29 Mar 2008 09:11:41 +0100</pubDate>
            <guid isPermaLink="false">1340893</guid>        </item>
        <item>
            <title>Safety of parathyroid hormone for the treatment of osteoporosis</title>
            <link>http://www.medworm.com/index.php?rid=1340895&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F3165336h16814241%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Teriparatide (recombinant human 1-34 parathyroid hormone) has been registered for the treatment of postmenopausal osteoporosis
 and osteoporosis in men for more than 5 years, whereas 1-84 parathyroid hormone has just recently been registered in Europe
 for osteoporosis management. Therefore, more data are available regarding the long-term safety of teriparatide. The issues
 to be considered are the effects of the registered dose of teriparatide (20 µg/day) on the incidence of hypercalcemia, hypercalciuria,
 and hyperuricemia, and the US Food and Drug Administration’s “black-box” warning regarding osteogenic sarcoma in the rat model.
 This review discusses these issues and provides the author’s extensive clinical experience and advice on the use of teriparatide
...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1340895</comments>
            <pubDate>Sat, 29 Mar 2008 09:11:40 +0100</pubDate>
            <guid isPermaLink="false">1340895</guid>        </item>
        <item>
            <title>Treatment of premenopausal women with low bone mineral density</title>
            <link>http://www.medworm.com/index.php?rid=1340896&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ft555737417636756%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Interpretation of bone mineral density (BMD) results in premenopausal women is particularly challenging, because the relationship
 between BMD and fracture risk is not the same as for postmenopausal women. Z scores rather than T scores should be used to
 define “low BMD” in premenopausal women. The finding of low BMD in a premenopausal woman should prompt an evaluation for secondary
 causes of bone loss. If a secondary cause is found, management should focus on treatment of this condition. In some cases
 in which the secondary cause cannot be addressed, such as glucocorticoid therapy or cancer chemotherapy, treatment with a
 bone-active agent to prevent bone loss should be considered. In women with no fractures and no known secondary cause, low
 BMD may not signify ...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1340896</comments>
            <pubDate>Sat, 29 Mar 2008 09:11:39 +0100</pubDate>
            <guid isPermaLink="false">1340896</guid>        </item>
        <item>
            <title>Treatment of children with osteogenesis imperfecta</title>
            <link>http://www.medworm.com/index.php?rid=853243&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu71u23323667g377%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Children with moderate to severe forms of osteogenesis imperfecta (OI) require adequate physiotherapy, rehabilitation and
 orthopedic surgery. Supportive treatment with bisphosphonates can improve the effects of these nonmedicinal treatment modalities.
 Benefits of bisphosphonate treatment include decreased pain, lower fracture incidence, and better mobility. Among the various
 bisphosphonates, intravenous pamidronate has been studied in most detail. However, the optimal treatment regimen and the long-term
 consequences of pamidronate treatment in children are currently unknown. Given these uncertainties, treatment with bisphosphonates
 during growth should be reserved for patients who have significant clinical problems, such as vertebral compression fractures
 or long-...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=853243</comments>
            <pubDate>Sat, 08 Sep 2007 04:34:51 +0100</pubDate>
            <guid isPermaLink="false">853243</guid>        </item>
        <item>
            <title>Prescreening tools to determine who needs DXA</title>
            <link>http://www.medworm.com/index.php?rid=853239&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb27031t863257k06%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Clinical decision rules (CDRs) are designed to help physicians practice better. A number of CDRs to assist in identifying
 women with low bone mass have been developed since the mid 1990s, including SCORE, OST (OSTA), OSIRIS, SOFSURF, NOF, ABONE,
 pBW, ORAI, and weight-only-EPIDOS (which we have termed WO-E). This review discusses these CDRs in terms of development and
 validation cohorts and their sensitivity and specificity. The sensitivities of the available CDRs exceed 80% and specificities
 are about 50%. After much analysis, it appears that most experts prefer OST for its simplicity and SCORE for its flexibility,
 but there is no consensus on what risk factors to use in the CDRs and what regions of interest (spine, total hip, femoral
 neck, or a combination) to te...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=853239</comments>
            <pubDate>Sat, 08 Sep 2007 04:34:51 +0100</pubDate>
            <guid isPermaLink="false">853239</guid>        </item>
        <item>
            <title>Osteoporosis and depression: A historical perspective</title>
            <link>http://www.medworm.com/index.php?rid=853232&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj48545w743334765%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;In the early 1980s, researchers studying osteoporosis noted that depression was one of the major negative consequences of
 bone loss and fractures. These researchers believed that osteoporosis and fractures occurred first, causing a reactive depression.
 Meanwhile, a similar but distinct psychiatry literature noted that osteoporosis or bone loss appeared to be an undesirable
 consequence of major depression. Here, depression was seen as the causal factor, and osteoporosis was the outcome. The psychiatric
 perspective is more biological, based on the presence of hypercorticoidism in depressed individuals. Those who believe that
 osteoporosis leads to depression point out that depression is a consequence of many chronic illnesses. Regardless of the correct
 causal order, ...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=853232</comments>
            <pubDate>Sat, 08 Sep 2007 04:34:51 +0100</pubDate>
            <guid isPermaLink="false">853232</guid>        </item>
        <item>
            <title>Exercise for people with osteoporosis: Translating the science into clinical practice</title>
            <link>http://www.medworm.com/index.php?rid=853231&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ft3051626142q782r%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The &quot;holy grail&quot; of inquiry regarding exercise and osteoporosis has been identifying a type of exercise that builds bone.
 Investigation using animal models has provided many insights into how bone responds to mechanical loading, but translating
 these findings into an exercise prescription for patients with osteoporosis is difficult. Patients expect bone to respond
 to exercise in a linear fashion, such as they are accustomed to experiencing with muscles in response to progressive strength
 training or with the cardiopulmonary system in response to endurance training. If the skeleton accrued greater mass in response
 to increasing intensity and duration of mechanical strain, our bones would weigh so much that we could not move. A unique
 requirement of bone is that ada...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=853231</comments>
            <pubDate>Sat, 08 Sep 2007 04:34:51 +0100</pubDate>
            <guid isPermaLink="false">853231</guid>        </item>
        <item>
            <title>Noninvasive assessment of bone microarchitecture by MRI</title>
            <link>http://www.medworm.com/index.php?rid=853229&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F360103237n87u631%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;In determining fracture risk, it has become apparent that bone mineral density accounts for only a portion of bone strength,
 with the remainder being determined by the material and structural properties of the bone tissue. Over the past 15 years,
 high-resolution MRI has provided a window into the structural nature of bone disease. Cross-sectional studies imaging the
 trabecular bone in patients with conditions ranging from postmenopausal osteoporosis to organ transplantation to renal osteodystrophy
 have all demonstrated a correlation of microarchitecture with fracture burden and have done so at a variety of anatomic sites.
 Recently, the utility of longitudinal studies for monitoring treatment in vivo has been demonstrated. This technique is noninvasive,
 involving n...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=853229</comments>
            <pubDate>Sat, 08 Sep 2007 04:34:51 +0100</pubDate>
            <guid isPermaLink="false">853229</guid>        </item>
        <item>
            <title>Stress fractures: Pathophysiology, epidemiology, and risk factors</title>
            <link>http://www.medworm.com/index.php?rid=853240&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh3240200h03n1873%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A stress fracture represents the inability of the skeleton to withstand repetitive bouts of mechanical loading, which results
 in structural fatigue and resultant signs and symptoms of localized pain and tenderness. To prevent stress fractures, an appreciation
 of their risk factors is required. These are typically grouped into extrinsic and intrinsic risk factors. Extrinsic risk factors
 for stress fractures are those in the environment or external to the individual, including the type of activity and factors
 involving training, equipment, and the environment. Intrinsic risk factors for stress fractures refer to characteristics within
 the individual, including skeletal, muscle, joint, and biomechanical factors, as well as physical fitness and gender. This
 article di...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=853240</comments>
            <pubDate>Sat, 08 Sep 2007 04:34:50 +0100</pubDate>
            <guid isPermaLink="false">853240</guid>        </item>
        <item>
            <title>Epidemiology and pathophysiology of osteoporosis in men</title>
            <link>http://www.medworm.com/index.php?rid=853235&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F26m023q6940u7407%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Osteoporosis in men is an unrecognized but growing problem as the number of men who live to old age increases. The 10-year
 fracture risk at age 50 quadruples by age 80, and in general the incidence rate of osteoporotic fracture in men is about half
 that of women. Of note, the mortality and morbidity after hip fracture are much greater in men. There are many men whose osteoporosis
 is the result of specific causes such as oral glucocorticoid therapy, hypogonadism, or androgen withdrawal therapy for prostate
 cancer. In addition there are several interesting syndromes of osteoporosis in middle-aged men; these men usually present
 with vertebral fractures. As knowledge about the prevalence and etiology of osteoporosis in men increases, it will be recognized
 and treated ...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=853235</comments>
            <pubDate>Sat, 08 Sep 2007 04:34:50 +0100</pubDate>
            <guid isPermaLink="false">853235</guid>        </item>
        <item>
            <title>Oral antiresorptive therapy</title>
            <link>http://www.medworm.com/index.php?rid=853241&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F051468218v577086%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Oral antiresorptive agents play a pivotal role in the management of osteoporosis. This paper discusses the effects and potential
 future role of newer agents such as ibandronate. Alternative dosing schedules and routes of administration have become available
 and may improve fracture protection, compliance, and tolerability for the long term treatment of a chronic condition such
 as osteoporosis. Increasingly these agents are being used to reduce bone loss in other diseases associated with high risk
 for osteoporosis such as organ transplantation and cystic fibrosis. Such studies may act as prototypes for the extended use
 of this class of drugs in other chronic inflammatory disease states. The innovative, yet disappointing results from combining
 an antiresorptive agen...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=853241</comments>
            <pubDate>Sat, 08 Sep 2007 04:34:49 +0100</pubDate>
            <guid isPermaLink="false">853241</guid>        </item>
        <item>
            <title>Web alert</title>
            <link>http://www.medworm.com/index.php?rid=853233&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq248p7272w043r10%2F</link>
            <description>Content TypeJournal Article

	
		JournalCurrent Osteoporosis ReportsOnline ISSN 1544-2241Print ISSN 1544-1873
	
		Journal VolumeVolume 4
	
		Journal IssueVolume 4, Number 3 / September, 2006 (Source: Current Osteoporosis Reports)</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=853233</comments>
            <pubDate>Sat, 08 Sep 2007 04:34:49 +0100</pubDate>
            <guid isPermaLink="false">853233</guid>        </item>
        <item>
            <title>Combination/sequential therapy in osteoporosis</title>
            <link>http://www.medworm.com/index.php?rid=853230&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy661585065r37nk3%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Combination therapy includes the concomitant or sequential use of compounds sharing the same mode of action (eg, two or more
 inhibitors of bone resorption) or with distinct pathways of activity (eg, an inhibitor of resorption plus an anabolic agent).
 Combination use of antiresorptive agents may generate concerns, because of the risk of inducing oversuppression of bone turnover.
 However, if low doses of estrogen, used for the management of climacteric symptoms, are insufficient to normalize bone turnover,
 the addition of a bisphosphonate to hormone therapy may prove to be useful to achieve this objective. Patients pretreated
 with inhibitors of resorption, who have not achieved a full therapeutic response, are good candidates for treatment with anabolic
 agents. The ...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=853230</comments>
            <pubDate>Sat, 08 Sep 2007 04:34:49 +0100</pubDate>
            <guid isPermaLink="false">853230</guid>        </item>
        <item>
            <title>Vertebroplasty and kyphoplasty: Rapid pain relief for vertebral compression fractures</title>
            <link>http://www.medworm.com/index.php?rid=853226&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp3052v74l0w0v216%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Vertebroplasty and kyphoplasty are minimally invasive procedures aimed at relieving symptoms associated with vertebral compression
 fractures. They have become accepted, highly effective, safe procedures, and are known for their high patient satisfaction
 rates. Although they are image-guided percutaneous spine therapies, differences do exist. They have each arisen from different
 backgrounds and are championed by different subspecialties and each involves slightly different techniques. In addition, a
 prospective, randomized trial comparing the two techniques has yet to be performed. This lack of objective data allows market
 forces and opinions to have a large influence on utilization and patient referral.
 
	Content TypeJournal Article

	
		JournalCurrent Osteoporosi...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=853226</comments>
            <pubDate>Sat, 08 Sep 2007 04:34:49 +0100</pubDate>
            <guid isPermaLink="false">853226</guid>        </item>
        <item>
            <title>Current technologies in the evaluation of bone architecture</title>
            <link>http://www.medworm.com/index.php?rid=853242&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw126220855618r51%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;In the context of osteoporosis, bone quality (which encompasses trabecular bone and cortical bone architecture), bone mineralization,
 turnover, and microdamage are all important, as are bone density and total content. Noninvasive assessment of bone quality
 has recently received considerable attention because bone density alone is not a surrogate for fracture prevalence and occurrence,
 and does not completely explain the therapeutic efficacy of emerging treatments. This paper focuses on the assessment of trabecular
 bone architecture, one of the factors that governs bone strength and may be categorized as a contributor to bone quality.
 The methodologies described include micro-computed tomography, magnetic resonance imaging, and computerized analysis of radiographic
...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=853242</comments>
            <pubDate>Sat, 08 Sep 2007 04:34:48 +0100</pubDate>
            <guid isPermaLink="false">853242</guid>        </item>
        <item>
            <title>Detection of vertebral fractures</title>
            <link>http://www.medworm.com/index.php?rid=853234&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F675v780g85tj1327%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Despite the importance of vertebral compression fractures, there is much that remains uncertain. There is no “gold standard“
 for the definition which has led to epidemiologic and study differences. Height loss is a way to suspect vertebral fractures
 but it has its own issues. There are multiple radiographic systems for defining vertebral fractures, both prevalent and incident;
 risk factors for prevalent fractures have already been delineated. Recent studies have elucidated the risk factors for incident
 vertebral fractures including age, low weight, late menarche, lower bone mineral density, history of vertebral and nonvertebral
 fractures, smoking, and use of a walking aid. Fan beam densitometers have had improving ability to image the spine, a procedure
 now kn...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=853234</comments>
            <pubDate>Sat, 08 Sep 2007 04:34:48 +0100</pubDate>
            <guid isPermaLink="false">853234</guid>        </item>
        <item>
            <title>Osteoprotegerin as a potential therapy for osteoporosis</title>
            <link>http://www.medworm.com/index.php?rid=853225&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn7515607831l7374%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The discovery and characterization of the RANKL/RANK/ OPG signaling pathway and the identification of its role in the pathogenesis
 of bone loss have provided the rationale for the development of drugs with the ability to modulate RANK-induced osteoclastogenesis.
 In vivo studies have identified interfering with the RANKL/RANK interaction as a potential therapeutic target in the management
 of osteoporosis. Two agents capable of blocking the binding of RANKL to RANK have been so far tested in clinical studies—osteoprotegerin
 (Fc-OPG fusion molecule) and the RANKL-antibody (AMG 162). Both have been found to have profound inhibitory effects on bone
 resorption, with AMG 162 appearing to be overall superior to OPG. Data are still very scarce, however, and much remains t...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=853225</comments>
            <pubDate>Sat, 08 Sep 2007 04:34:48 +0100</pubDate>
            <guid isPermaLink="false">853225</guid>        </item>
        <item>
            <title>Web alert</title>
            <link>http://www.medworm.com/index.php?rid=853224&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx284761011224k37%2F</link>
            <description>Content TypeJournal Article

	
		JournalCurrent Osteoporosis ReportsOnline ISSN 1544-2241Print ISSN 1544-1873
	
		Journal VolumeVolume 3
	
		Journal IssueVolume 3, Number 4 / December, 2005 (Source: Current Osteoporosis Reports)</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=853224</comments>
            <pubDate>Sat, 08 Sep 2007 04:34:48 +0100</pubDate>
            <guid isPermaLink="false">853224</guid>        </item>
        <item>
            <title>Use of highly potent bisphosphonates in the treatment of osteoporosis</title>
            <link>http://www.medworm.com/index.php?rid=853238&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl872638781t164w5%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Bisphosphonates are effective inhibitors of bone remodeling. In the clinical setting, these agents prevent bone loss, preserve
 bone architecture, and improve bone strength. Clinically significant reduction in the risk of spine and nonspine fractures
 is observed in patients known to be at risk for fracture. When administered appropriately, these drugs are well tolerated
 and have an excellent safety profile. Potent bisphosphonates are now the preferred treatment option to reduce the fracture
 risk in men and women with involutional and glucocorticoid-induced osteoporosis.
 
	Content TypeJournal Article

	
		JournalCurrent Osteoporosis ReportsOnline ISSN 1544-2241Print ISSN 1544-1873
	
		Journal VolumeVolume 1
	
		Journal IssueVolume 1, Number 3 / December, 2003 (Source...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=853238</comments>
            <pubDate>Sat, 08 Sep 2007 04:34:47 +0100</pubDate>
            <guid isPermaLink="false">853238</guid>        </item>
        <item>
            <title>Management of vitamin D depletion in postmenopausal women</title>
            <link>http://www.medworm.com/index.php?rid=853237&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc65h2jh166402454%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;In the United States, the impact regarding the routine fortification of milk and other dairy products has been less than satisfactory
 in preventing vitamin D depletion in adults. As more individuals are being evaluated and treated for osteoporosis, it has
 become necessary to exclude vitamin D depletion as a cause, because of the likelihood that differences in vitamin D and calcium
 nutrition may modify the individual response to therapy. Increased prevalence of subclinical vitamin D depletion among vertebral
 and hip fracture patients and the beneficial effect of vitamin D therapy and calcium supplementation in preventing such fractures
 lend credence to this assumption. The prevalence of vitamin D depletion is increasing again, especially among older adults,
 precise...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=853237</comments>
            <pubDate>Sat, 08 Sep 2007 04:34:47 +0100</pubDate>
            <guid isPermaLink="false">853237</guid>        </item>
        <item>
            <title>Web alert</title>
            <link>http://www.medworm.com/index.php?rid=853236&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fdpq325656w888125%2F</link>
            <description>Content TypeJournal Article

	
		JournalCurrent Osteoporosis ReportsOnline ISSN 1544-2241Print ISSN 1544-1873
	
		Journal VolumeVolume 1
	
		Journal IssueVolume 1, Number 3 / December, 2003 (Source: Current Osteoporosis Reports)</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=853236</comments>
            <pubDate>Sat, 08 Sep 2007 04:34:47 +0100</pubDate>
            <guid isPermaLink="false">853236</guid>        </item>
        <item>
            <title>Quantitative ultrasound: Use in the detection of fractures and in the assessment of bone composition</title>
            <link>http://www.medworm.com/index.php?rid=853228&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F580120328gh7701g%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Quantitative ultrasound (QUS) techniques have found widespread clinical use, but their specific role in clinical practice
 needs further refinement. This review discusses the ability of QUS approaches to predict the risk for prevalent vertebral
 fractures and the risk for future fractures. QUS approaches perform as well as central dual x-ray absorptiometry devices but
 with some disadvantages (at least for older QUS approaches) with regard to the predictive power for hip fractures. Technologic
 diversity of QUS approaches may lead to differences in performance. QUS also has the potential for assessing bone mineral
 density-independent aspects of bone composition that are relevant for bone strength. For measurements at the calcaneus, it
 is evident that bone microstructu...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=853228</comments>
            <pubDate>Sat, 08 Sep 2007 04:34:47 +0100</pubDate>
            <guid isPermaLink="false">853228</guid>        </item>
        <item>
            <title>Skeletal and nonskeletal effects of raloxifene</title>
            <link>http://www.medworm.com/index.php?rid=853227&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv75m101422v185q1%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Raloxifene, a selective estrogen receptor modulator, is approved for the prevention and treatment of postmenopausal osteoporosis.
 Prevention studies with raloxifene have demonstrated preservation of bone density and suppression of bone turnover markers
 in young postmenopausal women. The Multiple Outcomes of Raloxifene Evaluation study was the pivotal treatment trial for raloxifene.
 It demonstrated significant reduction in the risk for vertebral fractures after 1 and 3 years. Significant reduction of nonvertebral
 fractures with raloxifene has not yet been demonstrated. In addition to the effects of raloxifene on bone, potentially beneficial
 effects on the cardiovascular system, breast, and uterus have been described. Most of these nonskeletal effects have been
 repo...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=853227</comments>
            <pubDate>Sat, 08 Sep 2007 04:34:47 +0100</pubDate>
            <guid isPermaLink="false">853227</guid>        </item>
        <item>
            <title>Web alert</title>
            <link>http://www.medworm.com/index.php?rid=779059&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh37467q3l20qj716%2F</link>
            <description>Content TypeJournal Article

	
		JournalCurrent Osteoporosis ReportsOnline ISSN 1544-2241Print ISSN 1544-1873
	
		Journal VolumeVolume 4
	
		Journal IssueVolume 4, Number 3 / September, 1996 (Source: Current Osteoporosis Reports)</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=779059</comments>
            <pubDate>Mon, 11 Jun 2007 05:35:01 +0100</pubDate>
            <guid isPermaLink="false">779059</guid>        </item>
        <item>
            <title>The role of vitamin D for bone health and fracture prevention</title>
            <link>http://www.medworm.com/index.php?rid=779057&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F94527255626jh5k3%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Vitamin D inadequacy is pandemic in adults. Vitamin D deficiency causes osteopenia, precipitates and exacerbates osteoporosis,
 causes the painful bone disease osteomalacia, and increases muscle weakness, which worsens the risk of falls and fractures.
 Vitamin D deficiency can be prevented by sensible sun exposure and adequate supplementation. Monitoring serum 25-hydroxyvitamin
 D is the only way to determine vitamin D status. Recent recommendations suggest that in the absence of sun exposure, adults
 should ingest 1000 IU of vitamin D3 per day. The ideal healthy blood level of 25-hydroxyvitamin D should be 30 to 60 ng/mL. Vitamin D intoxication occurs when
 25-hydroxyvitamin D levels are greater than 150 ng/mL. Three recent reports suggesting that vitamin D and calcium...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=779057</comments>
            <pubDate>Mon, 11 Jun 2007 05:35:00 +0100</pubDate>
            <guid isPermaLink="false">779057</guid>        </item>
        <item>
            <title>Selecting patients for osteoporosis therapy</title>
            <link>http://www.medworm.com/index.php?rid=779055&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F111qkj046011587h%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;There is a global need to identify individuals at risk for osteoporotic fracture so that those at high risk can be treated
 and unnecessary treatment for those at low risk can be avoided. Bone mineral density (BMD) information is not sufficient to
 identify patients at high risk; approximately half of patients in the community with fractures do not have osteoporosis by
 the 1994 World Health Organization BMD criteria. Furthermore, BMD information is not easily accessible worldwide. The use
 of clinical risk factors with or without BMD information will improve our ability to identify patients at high risk for fracture.
 These risk factors can be integrated to predict a 10-year absolute risk or probability of fracture. Intervention thresholds
 based on absolute risk will ...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=779055</comments>
            <pubDate>Mon, 11 Jun 2007 05:34:59 +0100</pubDate>
            <guid isPermaLink="false">779055</guid>        </item>
        <item>
            <title>Stress fractures: Pathophysiology, epidemiology, and risk factors</title>
            <link>http://www.medworm.com/index.php?rid=779060&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq4g4g866252kk861%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A stress fracture represents the inability of the skeleton to withstand repetitive bouts of mechanical loading, which results
 in structural fatigue and resultant signs and symptoms of localized pain and tenderness. To prevent stress fractures, an appreciation
 of their risk factors is required. These are typically grouped into extrinsic and intrinsic risk factors. Extrinsic risk factors
 for stress fractures are those in the environment or external to the individual, including the type of activity and factors
 involving training, equipment, and the environment. Intrinsic risk factors for stress fractures refer to characteristics within
 the individual, including skeletal, muscle, joint, and biomechanical factors, as well as physical fitness and gender. This
 article di...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=779060</comments>
            <pubDate>Mon, 11 Jun 2007 05:34:58 +0100</pubDate>
            <guid isPermaLink="false">779060</guid>        </item>
        <item>
            <title>Epidemiology and pathophysiology of osteoporosis in men</title>
            <link>http://www.medworm.com/index.php?rid=779056&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg844141q83541037%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Osteoporosis in men is an unrecognized but growing problem as the number of men who live to old age increases. The 10-year
 fracture risk at age 50 quadruples by age 80, and in general the incidence rate of osteoporotic fracture in men is about half
 that of women. Of note, the mortality and morbidity after hip fracture are much greater in men. There are many men whose osteoporosis
 is the result of specific causes such as oral glucocorticoid therapy, hypogonadism, or androgen withdrawal therapy for prostate
 cancer. In addition there are several interesting syndromes of osteoporosis in middle-aged men; these men usually present
 with vertebral fractures. As knowledge about the prevalence and etiology of osteoporosis in men increases, it will be recognized
 and treated ...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=779056</comments>
            <pubDate>Mon, 11 Jun 2007 05:34:56 +0100</pubDate>
            <guid isPermaLink="false">779056</guid>        </item>
        <item>
            <title>Inflammatory bowel diseases as secondary causes of osteoporosis</title>
            <link>http://www.medworm.com/index.php?rid=779058&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F8vl26861831006t4%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Inflammatory bowel disease (IBD), comprising Crohn’s disease and ulcerative colitis, is associated with an increased risk
 of osteoporosis and bone fractures. Initial studies suggested very high rates of osteoporosis in IBD, but more recent studies
 have suggested that bone mineral density (BMD) is often normal in patients with IBD and typically changes little over time.
 Nonetheless, IBD is associated with an increased risk of fractures. Doctors managing patients with IBD must consider a variety
 of risk factors, not just BMD measurements, in assessing fracture risk. Advances have been made in exploring the pathogenesis
 of osteoporosis in IBD. The evolution of knowledge regarding receptor for activated factor of nuclear factor κB (RANK), its
 ligand RANKL, and oste...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=779058</comments>
            <pubDate>Mon, 11 Jun 2007 05:34:55 +0100</pubDate>
            <guid isPermaLink="false">779058</guid>        </item>
        <item>
            <title>Ibandronate treatment for osteoporosis: Rationale, preclinical and clinical development of extended dosing regimens</title>
            <link>http://www.medworm.com/index.php?rid=779067&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj5x787puxm364566%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Ibandronate is a potent nitrogen-containing bisphosphonate available as a once-monthly oral formulation for the treatment
 and prevention of osteoporosis. Preclinical experiments with estrogen-depleted rats, dogs, and monkeys demonstrated the efficacy
 of daily and intermittent ibandronate dosing. Initial clinical trials explored the optimal dosing regimens for oral administration
 in humans. The Oral Ibandronate Osteoporosis Vertebral Fracture Trial in North America and Europe (BONE) and Monthly Oral
 Ibandronate in Ladies (MOBILE) trials demonstrated that long-term daily and intermittent administration of ibandronate was
 efficacious for increasing bone mineral density, reducing markers of bone turnover, and preventing fractures, while maintaining
 bone quality. These...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=779067</comments>
            <pubDate>Sun, 03 Jun 2007 07:29:07 +0100</pubDate>
            <guid isPermaLink="false">779067</guid>        </item>
        <item>
            <title>Review of adherence to medications for the treatment of osteoporosis</title>
            <link>http://www.medworm.com/index.php?rid=779066&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa487137434wtw21t%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;One of the major challenges of successful osteoporosis management is poor patient adherence to current therapies. Individuals
 who are nonadherent have significant consequences of reduced bone mineral density response, reduced bone marker suppression,
 and increased risk for fracture compared with individuals who are adherent. Although reducing the dosing interval from daily
 to weekly oral bisphosphonates has improved adherence, adherence with weekly bisphosphonates remains suboptimal. Barriers
 to adherence include patient health beliefs, inadequate patient education and age. Potential solutions include increased health
 care provider-patient interaction, and longer times between doses of medications.
 
	Content TypeJournal Article

	
		JournalCurrent Osteoporosis Rep...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=779066</comments>
            <pubDate>Sun, 03 Jun 2007 07:29:06 +0100</pubDate>
            <guid isPermaLink="false">779066</guid>        </item>
        <item>
            <title>Web alert</title>
            <link>http://www.medworm.com/index.php?rid=779065&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F2r1758374233k013%2F</link>
            <description>Content TypeJournal Article

	
		JournalCurrent Osteoporosis ReportsOnline ISSN 1544-2241Print ISSN 1544-1873
	
		Journal VolumeVolume 4
	
		Journal IssueVolume 4, Number 1 / March, 2006 (Source: Current Osteoporosis Reports)</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=779065</comments>
            <pubDate>Sun, 03 Jun 2007 07:29:06 +0100</pubDate>
            <guid isPermaLink="false">779065</guid>        </item>
        <item>
            <title>The use of zoledronic acid for paget’s disease of bone</title>
            <link>http://www.medworm.com/index.php?rid=779061&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr707868905840781%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Paget’s disease of bone is a common skeletal disorder of the elderly that often results in significant morbidity and disability.
 Although there are a number of oral bisphosphonates currently available for treatment, normalization of biochemical markers
 of bone turnover with these agents is rarely accomplished due to difficulty with administration, adherence, and possibly resistance
 to individual bisphosphonates. This paper will focus on zoledronic acid, a potent and easily administered intravenous bisphosphonate
 that appears to result in a higher percentage of patients with normalization of markers of bone turnover and results in improvements
 in quality of life in patients with Paget’s disease of bone.
 
	Content TypeJournal Article

	
		JournalCurrent Osteopor...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=779061</comments>
            <pubDate>Sun, 03 Jun 2007 07:29:05 +0100</pubDate>
            <guid isPermaLink="false">779061</guid>        </item>
        <item>
            <title>Inhibition of RANKL as a treatment for osteoporosis: Preclinical and early clinical studies</title>
            <link>http://www.medworm.com/index.php?rid=779063&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh355n25886p616k4%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Osteoporosis and several other bone disorders occur when there is an imbalance between the resorption and formation components
 of bone remodeling activity. Therapies available for some of these conditions modulate the activity of osteoclasts and/or
 osteoblasts. The recent discoveries of receptor activator of NF-кB ligand (RANKL), an endogenous activator of osteoclastogenenesis
 and osteoclast activity and its inhibitor, osteoprotegerin (OPG) as pivotal regulatory factors in the pathogenesis of bone
 diseases like osteoporosis provide unique targets for therapeutic agents. In laboratory animals and now in humans, administering
 forms of OPG markedly inhibits osteoclast activity and improves bone strength, documenting that the strategy of inhibiting
 RANKL activity has...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=779063</comments>
            <pubDate>Sun, 03 Jun 2007 07:29:04 +0100</pubDate>
            <guid isPermaLink="false">779063</guid>        </item>
        <item>
            <title>Strontium ranelate—Data on vertebral and nonvertebral fracture efficacy and safety: Mechanism of action</title>
            <link>http://www.medworm.com/index.php?rid=779062&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F90526up67h6hn7t5%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Strontium ranelate is a novel therapy for the treatment of postmenopausal osteoporosis with actions to reduce bone resorption
 and increase bone formation. In vitro, strontium ranelate has anabolic and antiresorptive activity, increasing collagen and
 non-collagen protein synthesis, enhancing pre-osteoblast differentiation, inhibiting osteoclast differentiation, and reducing
 osteoclast function. In animal models, the increase in bone density is closely correlated with increases in biomechanical
 bone strength. Histomorphometry demonstrates reduced osteoclast surfaces with increased bone formation. Clinical trials in
 postmenopausal women have demonstrated 3-year fracture efficacy. Reductions in vertebral fracture were seen in patients with
 and without prevalent verteb...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=779062</comments>
            <pubDate>Sun, 03 Jun 2007 07:29:02 +0100</pubDate>
            <guid isPermaLink="false">779062</guid>        </item>
        <item>
            <title>Combination/sequential therapies for anabolic and antiresorptive skeletal agents for osteoporosis</title>
            <link>http://www.medworm.com/index.php?rid=779064&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F114l41150g7g8505%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;In this paper, we focus upon the use of anabolic skeletal therapy for the treatment of postmenopausal and other forms of osteoporosis.
 The only anabolic skeletal agent currently available is a recombinant bioactive fragment of parathyroid hormone, PTH(1-34),
 known as teriparatide. The full length molecule, human PTH(1-84) is being investigated at this time as are other PTH molecules.
 Teriparatide improves bone quality by actions on bone turnover, bone density, bone size, and microarchitecture. In postmenopausal
 women with osteoporosis, teriparatide reduces the incidence for vertebral and nonvertebral fractures. In individuals who have
 been treated previously with an antiresorptive agent, the subsequent actions of teriparatide on bone density are delayed transiently...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=779064</comments>
            <pubDate>Sun, 03 Jun 2007 07:29:00 +0100</pubDate>
            <guid isPermaLink="false">779064</guid>        </item>
        <item>
            <title>Bone density and markers of bone turnover in predicting fracture risk and how changes in these measures predict fracture risk reduction</title>
            <link>http://www.medworm.com/index.php?rid=779073&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fbrvv2543m0014657%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Surrogate markers in clinical medicine provide a useful means to assess therapeutic response to pharmacologic therapy in a
 wide range of chronic disease states. In the area of osteoporosis, the surrogate markers of change in bone mineral density
 (BMD) and bone turnover markers (BTM) provide the clinician with a means of assessing the biologic response to osteoporosis-specific
 pharmacologic agents. Increases in BMD and/or reductions in BTM can independently be correlated to reductions in vertebral
 and nonvertebral fracture risk. In managing osteoporosis patients, the BTM change at an earlier point of time after initiation
 of therapy and a change in BTM can provide earlier feed-back to the patient and clinician regarding issues such as compliance
 and a bone biologic...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=779073</comments>
            <pubDate>Sat, 02 Jun 2007 08:03:04 +0100</pubDate>
            <guid isPermaLink="false">779073</guid>        </item>
        <item>
            <title>Mechanisms of glucocorticoid action in bone</title>
            <link>http://www.medworm.com/index.php?rid=779071&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F3g1t503560021888%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Glucocorticoids induce rapid bone loss and increase the risk for osteoporotic fractures. The mechanisms include a phase of
 increased bone resorption, probably a result of the increased expression of receptor activator of nuclear factor-κ-B ligand
 and colony stimulating factor-1, followed-up by a decrease in bone formation. This effect is central to the actions of glucocorticoids
 in bone and it is secondary to the loss of bone forming cells, caused by an inhibition of cell differentiation and an increase
 in the apoptosis of mature osteoblasts and osteocytes. Glucocorticoids also inhibit the function of mature osteoblasts and
 suppress the synthesis of insulin-like growth factor-I, an agent that enhances bone formation. Glucocorticoids alter the growth
 hormone/insul...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=779071</comments>
            <pubDate>Sat, 02 Jun 2007 08:03:02 +0100</pubDate>
            <guid isPermaLink="false">779071</guid>        </item>
        <item>
            <title>Review of guidelines for bone mineral density testing and treatment of osteoporosis</title>
            <link>http://www.medworm.com/index.php?rid=779069&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fak737755042h2711%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Clinical practice guidelines (CPGs) are systematically developed statements intended to influence the behavior of health care
 providers and improve patient care. There are many CPGs with recommendations for selection of patients for bone mineral density
 testing and pharmacologic treatment of osteoporosis. Health care provider adherence rates for these CPGs are low. The multiplicity
 of osteoporosis CPGs directed to the same health care providers may play a role in their limited utilization in clinical practice.
 Similarities, differences, and conflicts in osteoporosis CPGs with wide distribution in the United States were examined. The
 analysis showed similarities as well as substantial variation in the patient populations addressed, inconsistency of some
 recommendat...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=779069</comments>
            <pubDate>Sat, 02 Jun 2007 08:02:57 +0100</pubDate>
            <guid isPermaLink="false">779069</guid>        </item>
        <item>
            <title>Osteoprotegerin as a potential therapy for osteoporosis</title>
            <link>http://www.medworm.com/index.php?rid=779074&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq0505837482v413g%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The discovery and characterization of the RANKL/RANK/ OPG signaling pathway and the identification of its role in the pathogenesis
 of bone loss have provided the rationale for the development of drugs with the ability to modulate RANK-induced osteoclastogenesis.
 In vivo studies have identified interfering with the RANKL/RANK interaction as a potential therapeutic target in the management
 of osteoporosis. Two agents capable of blocking the binding of RANKL to RANK have been so far tested in clinical studies—osteoprotegerin
 (Fc-OPG fusion molecule) and the RANKL-antibody (AMG 162). Both have been found to have profound inhibitory effects on bone
 resorption, with AMG 162 appearing to be overall superior to OPG. Data are still very scarce, however, and much remains t...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=779074</comments>
            <pubDate>Sat, 02 Jun 2007 08:02:47 +0100</pubDate>
            <guid isPermaLink="false">779074</guid>        </item>
        <item>
            <title>Treatment of children with osteogenesis imperfecta</title>
            <link>http://www.medworm.com/index.php?rid=779070&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F8248323144k8m4u8%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Children with moderate to severe forms of osteogenesis imperfecta (OI) require adequate physiotherapy, rehabilitation and
 orthopedic surgery. Supportive treatment with bisphosphonates can improve the effects of these nonmedicinal treatment modalities.
 Benefits of bisphosphonate treatment include decreased pain, lower fracture incidence, and better mobility. Among the various
 bisphosphonates, intravenous pamidronate has been studied in most detail. However, the optimal treatment regimen and the long-term
 consequences of pamidronate treatment in children are currently unknown. Given these uncertainties, treatment with bisphosphonates
 during growth should be reserved for patients who have significant clinical problems, such as vertebral compression fractures
 or long-...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=779070</comments>
            <pubDate>Sat, 02 Jun 2007 08:02:46 +0100</pubDate>
            <guid isPermaLink="false">779070</guid>        </item>
        <item>
            <title>Prescreening tools to determine who needs DXA</title>
            <link>http://www.medworm.com/index.php?rid=779072&amp;cid=s_35942_31_f&amp;fid=35942&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy14581331608h64t%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Clinical decision rules (CDRs) are designed to help physicians practice better. A number of CDRs to assist in identifying
 women with low bone mass have been developed since the mid 1990s, including SCORE, OST (OSTA), OSIRIS, SOFSURF, NOF, ABONE,
 pBW, ORAI, and weight-only-EPIDOS (which we have termed WO-E). This review discusses these CDRs in terms of development and
 validation cohorts and their sensitivity and specificity. The sensitivities of the available CDRs exceed 80% and specificities
 are about 50%. After much analysis, it appears that most experts prefer OST for its simplicity and SCORE for its flexibility,
 but there is no consensus on what risk factors to use in the CDRs and what regions of interest (spine, total hip, femoral
 neck, or a combination) to te...</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=779072</comments>
            <pubDate>Sat, 02 Jun 2007 08:02:42 +0100</pubDate>
            <guid isPermaLink="false">779072</guid>        </item>
        <item>
            <title>Web alert</title>
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            <description>Content TypeJournal Article

	
		JournalCurrent Osteoporosis ReportsOnline ISSN 1544-2241Print ISSN 1544-1873
	
		Journal VolumeVolume 4
	
		Journal IssueVolume 4, Number 4 / December, 1996 (Source: Current Osteoporosis Reports)</description>
            <author>Current Osteoporosis Reports</author>
            <type>journals</type>
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            <pubDate>Sat, 02 Jun 2007 08:02:32 +0100</pubDate>
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