Reviews in Endocrine & Metabolic Disorders
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Identification and treatment of metabolic complications in pediatric obesity
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Abstract Metabolic consequences of obesity including insulin resistance, type 2 diabetes mellitus, hyperlipidemia, hypertension, polycystic
ovarian syndrome, and non-alcoholic fatty liver infiltration are rapidly emerging in the pediatric population. Identifying
effective strategies for identifying and treating these obesity related co-morbidities in children are crucial to the prevention
of future cardiovascular disease and poor health outcomes. This review discusses the pathophysiologic connections between
obesity, metabolic disease and cardiovascular risk. Current evidence and recommendations for screenin...
Source: Reviews in Endocrine & Metabolic Disorders - October 7, 2009 Category: Endocrinology Tags: Reviews in Endocrine & Metabolic Disorders Source Type: journals
Fracture risk assessment in postmenopausal women
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Abstract Patients with osteoporosis have an increased risk of sustaining fractures because of the low bone mineral density (BMD) and
altered bone micro-architecture which are characteristic features of the disease. Although a good correlation exists between
BMD and fracture risks, many other factors influence this relationship. While there is consensus that patients with osteoporosis
should be investigated and treated, the issue is much less clear for patients with osteopenia. Because osteopenia is so prevalent,
it would be unrealistic to treat all patients with this condition. Therefore, there is a need to ...
Source: Reviews in Endocrine & Metabolic Disorders - October 1, 2009 Category: Endocrinology Tags: Reviews in Endocrine & Metabolic Disorders Source Type: journals
Role of biological rhythms in gastrointestinal health and disease
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Abstract The molecular basis for biological rhythms is formed by clock genes. Clock genes are functional in the liver, within gastrointestinal
epithelial cells and neurons of the enteric nervous system. These observations suggest a possible role for clock genes in
various circadian functions of the liver and the gastrointestinal tract through the modulation of organ specific clock-controlled
genes. Consequently, disruptions in circadian rhythmicity may lead to adverse health consequences. This review will focus
on the current understanding of the role of circadian rhythms in the pathogenesis of gastrointesti...
Source: Reviews in Endocrine & Metabolic Disorders - October 1, 2009 Category: Endocrinology Tags: Reviews in Endocrine & Metabolic Disorders Source Type: journals
Effects of circadian disruption on the cardiometabolic system
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Abstract The presence of day–night variations in cardiovascular and metabolic functioning is well known. However, only recently it
has been shown that cardiovascular and metabolic processes are not only affected by the behavioral sleep/wake cycle but are
partly under direct control of the master circadian pacemaker located in the suprachiasmatic nucleus (SCN). Heart rate, cardiac
autonomic activity, glucose metabolism and leptin—involved in appetite control—all show circadian variation (i.e., under constant
behavioral and environmental conditions). This knowledge of behavioral vs. circadian modulation ...
Source: Reviews in Endocrine & Metabolic Disorders - September 29, 2009 Category: Endocrinology Tags: Reviews in Endocrine & Metabolic Disorders Source Type: journals
Expression of clock genes in the suprachiasmatic nucleus: Effect of environmental lighting conditions
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Abstract The suprachiasmatic nucleus (SCN) is the anatomical substrate for the principal circadian clock coordinating daily rhythms
in a vast array of behavioral and physiological responses. Individual SCN neurons are cellular oscillators and are organized
into a multi-oscillator network following unique spatiotemporal patterns. The rhythms generated in the SCN are generally entrained
to the environmental light dark cycle, which is the most salient cue influencing the network organization of the SCN. The
neural network in the SCN is a heterogeneous structure, containing two major compartments identified by a...
Source: Reviews in Endocrine & Metabolic Disorders - September 24, 2009 Category: Endocrinology Tags: Reviews in Endocrine & Metabolic Disorders Source Type: journals
The current state of pediatric obesity treatment
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Content Type Journal ArticleDOI 10.1007/s11154-009-9114-8Authors
Brandon M. Nathan, University of Minnesota Division of Pediatric Endocrinology 420 Delaware Street SE, MMC 404 Minneapolis MN 55455 USA
Journal Reviews in Endocrine & Metabolic DisordersOnline ISSN 1573-2606Print ISSN 1389-9155
Source: Reviews in Endocrine & Metabolic Disorders - September 24, 2009 Category: Endocrinology Tags: Reviews in Endocrine & Metabolic Disorders Source Type: journals
The role of retinal photoreceptors in the regulation of circadian rhythms
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Abstract The circadian clock is an evolutionarily, highly conserved feature of most organisms. This internal timing mechanism coordinates
biochemical, physiological and behavioral processes to maintain synchrony with the environmental cycles of light, temperature
and nutrients. Several studies have shown that light is the most potent cue used by most organisms (humans included) to synchronize
daily activities. In mammals, light perception occurs only in the retina; three different types of photoreceptors are present
within this tissue: cones, rods and the newly discovered intrinsically photosensitive retinal...
Source: Reviews in Endocrine & Metabolic Disorders - September 24, 2009 Category: Endocrinology Tags: Reviews in Endocrine & Metabolic Disorders Source Type: journals
Physiological responses of the circadian clock to acute light exposure at night
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Abstract Circadian rhythms in physiological, endocrine and metabolic functioning are controlled by a neural clock located in the suprachiasmatic
nucleus (SCN). This structure is endogenously rhythmic and the phase of this rhythm can be reset by light information from
the eye. A key feature of the SCN is that while it is a small structure containing on the order of about 20,000 cells, it
is amazingly heterogeneous. It is likely that anatomical heterogeneity reflects an underlying functional heterogeneity. In
this review, we examine the physiological responses of cells in the SCN to light stimuli that reset th...
Source: Reviews in Endocrine & Metabolic Disorders - September 18, 2009 Category: Endocrinology Tags: Reviews in Endocrine & Metabolic Disorders Source Type: journals
The surgical approach to management of pediatric obesity: When to refer and what to expect
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Abstract Weight loss surgery is recommended for adult patients with morbid obesity and has been used on a case by case basis in the
pediatric population. Surgery, however, is just a tool added to the two mainstays of therapy for obesity: 1.) controlled dietary
intake and 2.) increases in activity and exercise behaviors. For the pediatric population, the health consequences of obesity
are profound with increased cardiovascular risk during adolescence and increased mortality in adulthood. Currently accepted
guidelines for weight loss surgery referral use BMI cut points that are the same as for adults: BMI ...
Source: Reviews in Endocrine & Metabolic Disorders - September 3, 2009 Category: Endocrinology Tags: Reviews in Endocrine & Metabolic Disorders Source Type: journals
Effective dietary therapies for pediatric obesity treatment
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Abstract Dietary changes combined with behavioral management techniques, such as short term attainable goal setting, is effective for
treating pediatric obesity. Dietary interventions combined with increasing physical activity are essential for weight loss.
We review the basic nutrition concepts that should be employed to treat pediatric obesity and summarize the available literature
on effective dietary interventions that have been studied to date.
Content Type Journal ArticleDOI 10.1007/s11154-009-9113-9Authors
Angela Fitch, University of Minnesota Internal Medicine and Pediatrics, Pediatric Weight Man...
Source: Reviews in Endocrine & Metabolic Disorders - August 25, 2009 Category: Endocrinology Tags: Reviews in Endocrine & Metabolic Disorders Source Type: journals
Pharmacotherapy in pediatric obesity: Current agents and future directions
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Abstract Childhood obesity is emerging as a major public health threat, with adverse implications on the health of individuals and
long-term costs to society. Family-based lifestyle interventions with behavioral modification, diet and exercise form the
mainstay of treatment. Pharmacologic treatment may be considered in selected subjects, especially in the presence of significant
and severe comorbidities, when lifestyle intervention has failed to achieve weight reduction. Orlistat and sibutramine are
FDA-approved for treatment of pediatric obesity; metformin may be considered in the presence of clinically sig...
Source: Reviews in Endocrine & Metabolic Disorders - August 17, 2009 Category: Endocrinology Tags: Reviews in Endocrine & Metabolic Disorders Source Type: journals
Designing and implementing an effective pediatric weight management program
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Abstract In order to successfully address the problem of childhood obesity, effective weight management programs must be established
by a variety of clinicians to treat the increasing numbers of overweight and obese children and adolescents. An effective
program will: 1) identify children and adolescents with health risks related to excess fat, 2) help families make permanent
healthy lifestyle changes, and 3) provide ongoing care to optimize long-term health. Building a pediatric weight management
program which achieves these goals requires attention to several aspects, including location, personnel, equipme...
Source: Reviews in Endocrine & Metabolic Disorders - June 25, 2009 Category: Endocrinology Tags: Reviews in Endocrine & Metabolic Disorders Source Type: journals
The influence of fitness on insulin resistance in obese children
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Abstract An increasingly pervasive environment of reduced activity and easy access to high caloric food is leading to an epidemic of
poor cardiovascular fitness, obesity, insulin resistance and type 2 diabetes (T2DM) in children. Studies have shown that insulin
resistance (IR) to be an independent predictor for morbidity as well as mortality. These serve as a strong stimulus for public
health strategies to improve fitness in children and adolescents. Methods to assess IR, improve IR and understand complications
are increasingly important in children.
Content Type Journal ArticleDOI 10.1007/s11154-009-9109...
Source: Reviews in Endocrine & Metabolic Disorders - May 29, 2009 Category: Endocrinology Tags: Reviews in Endocrine & Metabolic Disorders Source Type: journals
Adrenarche
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Content Type Journal ArticleDOI 10.1007/s11154-009-9108-6Authors
Sharon E. Oberfield, NewYork-Presbyterian Hospital/Columbia University Medical Center 630 West 168th Street New York NY 10032 USAPerrin C. White, UT Southwestern Medical Center 5323 Harry Hines Boulevard Dallas TX 75390-9063 USA
Journal Reviews in Endocrine & Metabolic DisordersOnline ISSN 1573-2606Print ISSN 1389-9155
Source: Reviews in Endocrine & Metabolic Disorders - February 24, 2009 Category: Endocrinology Tags: Reviews in Endocrine & Metabolic Disorders Source Type: journals
Androgen synthesis in adrenarche
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Abstract The enzymes and pathways of steroidogenesis are central to an understanding of adrenarche. The quantitative regulation of
steroidogenesis occurs at the first step, the conversion of cholesterol to pregnenolone. Chronic quantitative regulation is
principally at the level of transcription of the CYP11A1 gene encoding P450scc, which is the enzymatically rate-limiting step.
Acute regulation is mediated by the steroidogenic acute regulatory protein (StAR), which facilitates the rapid influx of cholesterol
into mitochondria, where P450scc resides. Qualitative regulation, which determines the type of stero...
Source: Reviews in Endocrine & Metabolic Disorders - September 27, 2008 Category: Endocrinology Tags: Reviews in Endocrine & Metabolic Disorders Source Type: journals
Adrenal changes associated with adrenarche
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This article reviews the intra-adrenal changes of the adrenal cortex associated with
adrenarche.
Content Type Journal ArticleDOI 10.1007/s11154-008-9092-2Authors
Yasuhiro Nakamura, Medical College of Georgia Department of Physiology 1120 15th Street Augusta GA 30912 USAHui Xiao Gang, Tohoku University Graduate School of Medicine Department of Pathology Sendai 980-8575 JapanTakashi Suzuki, Tohoku University Graduate School of Medicine Department of Pathology Sendai 980-8575 JapanHironobu Sasano, Tohoku University Graduate School of Medicine Department of Pathology Sendai 980-8575 JapanWilliam E. Rainey, Medical Colleg...
Source: Reviews in Endocrine & Metabolic Disorders - September 27, 2008 Category: Endocrinology Tags: Reviews in Endocrine & Metabolic Disorders Source Type: journals
Expression of the IGF and the aromatase/estrogen receptor systems in human adrenal tissues from early infancy to late puberty: Implications for the development of adrenarche
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Abstract Adrenarche is a process of postnatal sexual maturation occurring in higher primates, in which there is an increase in the
secretion of adrenal androgens. It is the consequence of a process of postnatal organogenesis characterized by the development
of a new zone in the adrenal cortex, the zona reticularis (ZR). The mechanism of this phenomenon remains poorly understood,
suggesting that it might be a multifactorial event. A relationship between circulating IGF-I, insulin sensitivity, and adrenal
androgens has been postulated. Boys and girls have different patterns of changes in insulin sensitivity at...
Source: Reviews in Endocrine & Metabolic Disorders - September 16, 2008 Category: Endocrinology Tags: Reviews in Endocrine & Metabolic Disorders Source Type: journals
Medical therapy of pituitary adenomas: Effects on tumor shrinkage
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Abstract The efficacy of dopamine-agonists (DA) in patients with prolactinomas and that of somatostatin analogues (SSA) in those with
GH- and TSH-secreting adenomas is well established. More recently, data are accumulating suggesting a potential therapeutic
role of DA also in patients with ACTH-secreting and clinically non-functioning (NFA) pituitary adenomas. This review aims
at summarizing published results of DA and SSA on tumor shrinkage in patients with different histotypes of pituitary adenomas.
Results of tumor shrinkage are of clinical relevance as tumor size is the one of the most important determin...
Source: Reviews in Endocrine & Metabolic Disorders - September 13, 2008 Category: Endocrinology Tags: Reviews in Endocrine & Metabolic Disorders Source Type: journals
Modern techniques for pituitary radiotherapy
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Abstract Radiotherapy (RT) remains an effective treatment for residual or recurrent pituitary adenomas with excellent rates of tumour
control and normalisation of excess hormone secretion. The main late toxicity is hypopituitarism: other side effects are rare.
We discuss technical developments in the delivery of radiotherapy (stereotactic conformal radiotherapy (SCRT) and stereotactic
radiosurgery (SRS)), all aiming to reduce the amount of normal brain receiving significant doses of radiation. We provide
a comprehensive review of published data on outcome of conventional fractionated radiotherapy and modern ...
Source: Reviews in Endocrine & Metabolic Disorders - September 12, 2008 Category: Endocrinology Tags: Reviews in Endocrine & Metabolic Disorders Source Type: journals
β
-cell failure as a complication of diabetes
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Abstract Type 2 diabetes mellitus is a complex disease characterized by β-cell failure in the setting of insulin resistance. In early stages of the disease, pancreatic β-cells adapt to insulin resistance by increasing mass and function. As nutrient excess persists, hyperglycemia and elevated
free fatty acids negatively impact β-cell function. This happens by numerous mechanisms, including the generation of reactive oxygen species, alterations in metabolic
pathways, increases in intracellular calcium and the activation of endoplasmic reticulum stress. These processes adversely
affect β-cells by impairing i...
Source: Reviews in Endocrine & Metabolic Disorders - September 8, 2008 Category: Endocrinology Tags: Reviews in Endocrine & Metabolic Disorders Source Type: journals
Mass spectrometric quantification of amino acid oxidation products identifies oxidative mechanisms of diabetic end-organ damage
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Abstract Diabetes mellitus is increasingly prevalent worldwide. Diabetic individuals are at markedly increased risk for premature death
due to cardiovascular disease. Furthermore, substantial morbidity results from microvascular complications which include retinopathy,
nephropathy, and neuropathy. Clinical studies involving diabetic patients have suggested that degree of diabetic hyperglycemia
correlates with risk of complications. Recent evidence implicates a central role for oxidative stress and vascular inflammation
in all forms of insulin resistance, obesity, diabetes and its complications. Although, glu...
Source: Reviews in Endocrine & Metabolic Disorders - August 28, 2008 Category: Endocrinology Tags: Reviews in Endocrine & Metabolic Disorders Source Type: journals
Clinical spectrum of premature pubarche: Links to metabolic syndrome and ovarian hyperandrogenism
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Abstract Premature pubarche—defined as the appearance of pubic hair before age 8 years in girls and 9 years in boys—has been traditionally
considered a benign entity. However, recent evidence supports the notion that premature pubarche in girls may be a forerunner
of the metabolic syndrome, and may precede the development of clinical ovarian androgen excess in adolescence. This sequence
seems to occur more frequently when premature pubarche was preceded by reduced fetal growth and followed by excessive postnatal
catch-up in height and particularly in weight; hyperinsulinemia appears to be a key...
Source: Reviews in Endocrine & Metabolic Disorders - August 26, 2008 Category: Endocrinology Tags: Reviews in Endocrine & Metabolic Disorders Source Type: journals
New insights into the mechanisms of fibrosis and sclerosis in diabetic nephropathy
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Abstract Progression of diabetic nephropathy (DN) is manifested by gradual scarring of both the renal glomerulus and tubulointerstitial
region. Over the past several years, the general understanding of the pathogenic factors that lead to renal fibrosis in DN
has expanded considerably. In this review, some of the important factors that appear to be involved in driving this fibrosing
process are discussed, with special emphasis on newer findings and insights. It is now clear that multiple cell types in the
kidney contribute to progressive fibrosis in DN. New concepts about bradykinin, TGF-β and eNOS signaling...
Source: Reviews in Endocrine & Metabolic Disorders - August 24, 2008 Category: Endocrinology Tags: Reviews in Endocrine & Metabolic Disorders Source Type: journals
Non-traditional metabolic pathways of adrenal steroids
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Abstract Metabolic pathways are reconstructed from biochemical evidence to conceptualize the predominant route to important biomolecules.
Pathways have heuristic value in their capacity to explain the metabolic derangements in genetic diseases of enzyme deficiencies
and during pharmacologic inhibition of these enzymes. Implicit in the description of these pathways is the potential existence
of alternate routes, variable order of reactions, and the inevitable by-products generated by incomplete efficiencies and
competing enzymes. This chapter will consider alternate fates encountered by steroid hormone precur...
Source: Reviews in Endocrine & Metabolic Disorders - August 22, 2008 Category: Endocrinology Tags: Reviews in Endocrine & Metabolic Disorders Source Type: journals
Mechanisms of disease: The oxidative stress theory of diabetic neuropathy
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Abstract Diabetic neuropathy is the most common complication of diabetes, affecting 50% of diabetic patients. Currently, the only treatment
for diabetic neuropathy is glucose control and careful foot care. In this review, we discuss the idea that excess glucose
overloads the electron transport chain, leading to the production of superoxides and subsequent mitochondrial and cytosolic
oxidative stress. Defects in metabolic and vascular pathways intersect with oxidative stress to produce the onset and progression
of nerve injury present in diabetic neuropathy. These pathways include the production of advanced g...
Source: Reviews in Endocrine & Metabolic Disorders - August 16, 2008 Category: Endocrinology Tags: Reviews in Endocrine & Metabolic Disorders Source Type: journals
Defining human diabetic nephropathy on the molecular level: Integration of transcriptomic profiles with biological knowledge
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Abstract Diabetic nephropathy (DN) is the most common cause for end stage renal disease (ESRD). Next to environmental factors, genetic
predispositions determine the susceptibility for DN and its rate of progression to ESRD. With the availability of genome wide
expression profiling we have the opportunity to define relevant pathways activated in the individual diabetic patient, integrating
both environmental exposure and genetic background. In this review we summarize current understanding of how to link comprehensive
gene expression data sets with biomedical knowledge and present strategies to build a transc...
Source: Reviews in Endocrine & Metabolic Disorders - August 15, 2008 Category: Endocrinology Tags: Reviews in Endocrine & Metabolic Disorders Source Type: journals
Nonclassic adrenal hyperplasia
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This article will review relevant clinical, hormonal and genetic aspects of nonclassic adrenal hyperplasia.
Content Type Journal ArticleDOI 10.1007/s11154-008-9097-xAuthors
Phyllis W. Speiser, Schneider Children’s Hospital 269-01 76th Ave. New Hyde Park NY 11040 USA
Journal Reviews in Endocrine & Metabolic DisordersOnline ISSN 1573-2606Print ISSN 1389-9155
Source: Reviews in Endocrine & Metabolic Disorders - August 9, 2008 Category: Endocrinology Tags: Reviews in Endocrine & Metabolic Disorders Source Type: journals
Nonhuman primates as models for human adrenal androgen production: Function and dysfunction
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Abstract The origin of circulating DHEA and adrenal-derived androgens in humans and nonhuman primates is largely distinct from other
mammalian species. In humans and many Old world primates, the fetal adrenal gland and adult zona reticularis (ZR) are known
to be the source for production of DHEA (and DHEAS) in mg quantities. In spite of similarities there are also some differences.
Herein, we take a comparative endocrine approach to the diversity of adrenal androgen biosynthesis and its developmental timing
in three primate species to illustrate how understanding such differences may provide unique insight i...
Source: Reviews in Endocrine & Metabolic Disorders - August 6, 2008 Category: Endocrinology Tags: Reviews in Endocrine & Metabolic Disorders Source Type: journals
The adrenal cortex and sexual differentiation during early human development
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Abstract Human sexual differentiation is a critical process whereby a strict dimorphism is established that enables future reproductive
success as phenotypic males and females. Significant components of this differentiation pathway unfold during the first three
months of gestation when they are sensitive to disruption by abnormal hormonal influences. Excessive exposure of female development
to androgens in conditions such as congenital adrenal hyperplasia causes virilization. However, recently we have suggested
that female development normally takes place in the presence of low, yet significant, levels of an...
Source: Reviews in Endocrine & Metabolic Disorders - August 1, 2008 Category: Endocrinology Tags: Reviews in Endocrine & Metabolic Disorders Source Type: journals
Iodine deficiency disorders and their prevention in India
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Abstract New insights on the high prevalence of functional decompensation of the thyroid among newborn and children from several states
of India as well as neighbouring countries of Nepal and Bhutan helped to prevent nutritional iodine deficiency and iodine
deficiency disorders through country-wide iodized salt prophylaxis. Presently on the basis of scientific studies, salt iodization
in India is saving millions of children from neonatal hypothyroidism related psycho-physical retardation.
Content Type Journal ArticleDOI 10.1007/s11154-008-9094-0Authors
N. Kochupillai, M. S. Ramaiah Medical College and Ho...
Source: Reviews in Endocrine & Metabolic Disorders - July 29, 2008 Category: Endocrinology Tags: Reviews in Endocrine & Metabolic Disorders Source Type: journals
Maternal nutrition, intrauterine programming and consequential risks in the offspring
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Abstract It is traditionally believed that genetic susceptibility and adult faulty lifestyle lead to type 2 diabetes, a chronic non-communicable
disease. The “Developmental Origins of Health and Disease” (DOHaD) model proposes that the susceptibility to type 2 diabetes
originates in the intrauterine life by environmental fetal programming, further exaggerated by rapid childhood growth, i.e.
a biphasic nutritional insult. Both fetal under nutrition (sometimes manifested as low birth weight) and over nutrition (the
baby of a diabetic mother) increase the risk of future diabetes. The common characteristic o...
Source: Reviews in Endocrine & Metabolic Disorders - July 26, 2008 Category: Endocrinology Tags: Reviews in Endocrine & Metabolic Disorders Source Type: journals
Oxidative stress and diabetic retinopathy: Pathophysiological mechanisms and treatment perspectives
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Abstract Retinopathy is one of the most severe ocular complications of diabetes and is a leading cause of acquired blindness in young
adults. The cellular components of the retina are highly coordinated but very susceptible to the hyperglycemic environment.
The microvasculature of the retina responds to hyperglycemic milieu through a number of biochemical changes, including increased
oxidative stress and polyol pathway, PKC activation and advanced glycation end product formation. Oxidative stress is considered
as one of the crucial contributors in the pathogenesis of diabetic retinopathy, but oxidative stres...
Source: Reviews in Endocrine & Metabolic Disorders - July 25, 2008 Category: Endocrinology Tags: Reviews in Endocrine & Metabolic Disorders Source Type: journals
Novel mechanisms of protein synthesis in diabetic nephropathy—role of mRNA translation
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Abstract Ambient protein levels are affected by both synthesis and degradation. Synthesis of a protein is regulated by transcription
and messenger RNA (mRNA) translation. Translation has emerged as an important site of regulation of protein expression during
development and disease. It is under the control of distinct factors that regulate initiation, elongation and termination
phases. Regulation of translation occurs via signaling reactions, guanosine diphosphate–guanosine triphosphate binding and
by participation of non-coding RNA species such as microRNA. Recent work has revealed an important role for t...
Source: Reviews in Endocrine & Metabolic Disorders - July 25, 2008 Category: Endocrinology Tags: Reviews in Endocrine & Metabolic Disorders Source Type: journals
Somatostatin–dopamine ligands in the treatment of pituitary adenomas
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Abstract Somatostatin receptors (sst1–5) and dopamine receptor 2 (D2DR) are well expressed and co-localized in several human pituitary
adenomas, suggesting possible functional interactions in the control of hormonal hypersecretion and tumor cell growth. The
present review describes the expression and functionality of these receptors in the different classes of human pituitary adenomas.
The sst2 agonists, octreotide and lanreotide, control GH hypersecretion and tumor growth in about 65% of somatotropinomas.
The D2DR agonists, bromocriptine and cabergoline, control about 90% of prolactinomas. Such drugs are ...
Source: Reviews in Endocrine & Metabolic Disorders - July 24, 2008 Category: Endocrinology Tags: Reviews in Endocrine & Metabolic Disorders Source Type: journals
Somatostatin and dopamine receptors as targets for medical treatment of Cushing’s Syndrome
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Abstract Somatostatin (SS) and dopamine (DA) receptors are widely expressed in neuroendocrine tumours that cause Cushing’s Syndrome
(CS). Increasing knowledge of specific subtype expression within these tumours and the ability to target these receptor subtypes
with high-affinity compounds, has driven the search for new SS- or DA-based medical therapies for the various forms of CS.
In Cushing’s disease, corticotroph adenomas mainly express dopamine receptor subtype 2 (D2) and somatostatin receptor subtype 5 (sst5), whereas sst2 is expressed at lower levels. Activation of these receptors can inhibit ACTH-re...
Source: Reviews in Endocrine & Metabolic Disorders - July 19, 2008 Category: Endocrinology Tags: Reviews in Endocrine & Metabolic Disorders Source Type: journals
Disorders of sex development (DSDs), their presentation and management in different cultures
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Abstract The way disorders of sex development (DSD) are viewed and managed in different cultures varies widely. They are complex conditions
and even well-educated lay people find them difficult to understand, but when families are very poor and lacking in basic
education, and the health system is starved of resources, traditional beliefs, folk remedies and prejudice combine to make
the lives of children and adults with DSD extremely difficult and sad. Rumour and discrimination isolate them from their communities
and they become devalued. People with DSDs desire the same things in life as everyone else—to f...
Source: Reviews in Endocrine & Metabolic Disorders - July 17, 2008 Category: Endocrinology Tags: Reviews in Endocrine & Metabolic Disorders Source Type: journals
Growth hormone receptor modulators
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Abstract Growth hormone (GH) regulates somatic growth, substrate metabolism and body composition. Its actions are elaborated through
the GH receptor (GHR). GHR signalling involves the role of at least three major pathways, STATs, MAPK, and PI3-kinase/Akt.
GH receptor function can be modulated by changes to the ligand, to the receptor or by factors regulating signal transduction.
Insights on the physico-chemical basis of the binding of GH to its receptor and the stoichiometry required for activation
of the GH receptor-dimer has led to the development of novel GH agonists and antagonists. Owing to the fact tha...
Source: Reviews in Endocrine & Metabolic Disorders - July 12, 2008 Category: Endocrinology Tags: Reviews in Endocrine & Metabolic Disorders Source Type: journals
Genetic aspects of tropical calcific pancreatitis
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Abstract Tropical calcific pancreatitis (TCP) is a subtype of chronic pancreatitis which is unique to tropical regions. Patients present
at young age with recurrent abdominal pain, nutritional deficiencies, and insulin-requiring diabetes. For a long time, the
aetiology of this disorder was poorly understood. Several environmental factors, such as malnutrition or the consumption of
toxic food components such as cyanogenic glycosides, were proposed as pathogenic factors. In the last decade, a major impact
on the understanding of the aetiology of TCP has come from genetic studies on hereditary and idiopathic ch...
Source: Reviews in Endocrine & Metabolic Disorders - July 7, 2008 Category: Endocrinology Tags: Reviews in Endocrine & Metabolic Disorders Source Type: journals
Potential of retinoic acid derivatives for the treatment of corticotroph pituitary adenomas
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Abstract Cushing’s disease is a severe clinical condition caused by hypersecretion of corticosteroids due to excessive ACTH secretion
from a pituitary adenoma. This complex endocrine disorder still represents a major challenge for the physician in terms of
efficient treatment. In the last years there was only little progress in elucidating the molecular mechanisms responsible
for the constitutive and autonomous ACTH secretion of pituitary corticotrophinomas. As a consequence, no effective drug therapy
is currently available, particularly if surgical excision is not successful. In the present article we exa...
Source: Reviews in Endocrine & Metabolic Disorders - July 6, 2008 Category: Endocrinology Tags: Reviews in Endocrine & Metabolic Disorders Source Type: journals
Potential role of type I interferons in the treatment of pituitary adenomas
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This article reviews the current knowledge about the effects of IFN-α and IFN-β on hypothalamic–pituitary function
and describes the potential role of type I IFNs in the treatment of pituitary adenomas.
Content Type Journal ArticleDOI 10.1007/s11154-008-9083-3Authors
Giovanni Vitale, University of Milan Istituto Auxologico Italiano IRCCS Via Zucchi 18 Cusano Milanino 20095 Milan ItalyMichele Caraglia, National Cancer Institute Fondazione “G. Pascale” Experimental Pharmacology Unit, Experimental Oncology Department Naples ItalyPeter M. van Koetsveld, Erasmus Medical Center Department of Internal Medicine Rotte...
Source: Reviews in Endocrine & Metabolic Disorders - July 6, 2008 Category: Endocrinology Tags: Reviews in Endocrine & Metabolic Disorders Source Type: journals
Advantages and disadvantages of GH/IGF-I combination treatment
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In conclusion, there are many
reasons for believing that administration of the combination therapy of GH and IGF-I could have advantages above GH alone
or IGF-I alone. However, determination of whether co-administration of GH and IGF-I indeed is superior to either agent alone
awaits further study.
Content Type Journal ArticleDOI 10.1007/s11154-008-9081-5Authors
J. A. M. J. L. Janssen, Erasmus MC Department of Internal Medicine Room D425, ‘s-Gravendijkwal 230 3015 CE Rotterdam The Netherlands
Journal Reviews in Endocrine & Metabolic DisordersOnline ISSN 1573-2606Print ISSN 1389-9155
Source: Reviews in Endocrine & Metabolic Disorders - July 6, 2008 Category: Endocrinology Tags: Reviews in Endocrine & Metabolic Disorders Source Type: journals
Pediatric vitamin D and calcium nutrition in developing countries
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Abstract Over one billion humans have insufficient circulating levels of vitamin D, and dietary insufficiency of calcium is common
in developing countries. Worldwide, nutritional rickets is considered to be the most common non-communicable disease of children.
Rickets can be due either to primary deficiencies of vitamin D or calcium or to combined deficiencies of both elements. Vitamin
D deficiency is also increasingly linked to non-skeletal complications. Even without laboratory and radiologic resources,
the diagnosis of rickets is considered clinically when a child presents with limb deformities and has be...
Source: Reviews in Endocrine & Metabolic Disorders - July 6, 2008 Category: Endocrinology Tags: Reviews in Endocrine & Metabolic Disorders Source Type: journals
Early diagnosis and prevention of diabetes in developing countries
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Abstract Type 2 diabetes has an insidious onset with a long latent period of dysglycaemia. By the time the diagnosis of diabetes is
made, diabetes-related tissue damage occurs in nearly half of the patients. Even after diagnosis, the glycaemic control is
suboptimal in more than 50%, leading to the vascular complications. Evidences suggest that early detection of diabetes by
appropriate screening methods, especially in subjects with high risk for diabetes will help to prevent or delay the vascular
complications and thus reduce the clinical, social and economic burden of the disease. There are also evidences t...
Source: Reviews in Endocrine & Metabolic Disorders - July 6, 2008 Category: Endocrinology Tags: Reviews in Endocrine & Metabolic Disorders Source Type: journals
Proteoglycan mediated lipoprotein retention: A mechanism of diabetic atherosclerosis
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Abstract The response to retention hypothesis outlines the initial stages of atherosclerotic lesion formation. The central theme of
the hypothesis is that proteoglycan mediated lipoprotein retention plays a critical step in the initiation of atherosclerosis
development. Recent research using human arterial specimens, transgenic mouse models and molecular biology techniques have
added to our understanding of atherosclerosis development, and provided experimental data in support of the response to retention
hypothesis. In this review we summarize the recent data, in particular that which addresses mechanisms b...
Source: Reviews in Endocrine & Metabolic Disorders - June 27, 2008 Category: Endocrinology Tags: Reviews in Endocrine & Metabolic Disorders Source Type: journals
Fracture risk and bone mineral density in Turner syndrome
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Abstract Bone health is a major lifelong concern in caring for women and girls with Turner syndrome (TS). There is an approximately
25% increase in fracture risk most of which is related to medium or high impact trauma. The long bones, especially of the
forearm are predominantly affected. This fact may be due to a selective cortical bone deficiency in TS which is unrelated
to hypogonadism. In addition, lack of adequate estrogen replacement can lead to trabecular bone deficiency and increase in
vertebral compression fractures after age 45. Evaluation of bone density by dual X-ray absorptiometry (DEXA) is impo...
Source: Reviews in Endocrine & Metabolic Disorders - April 15, 2008 Category: Endocrinology Tags: Reviews in Endocrine & Metabolic Disorders Source Type: journals
Bone density in the adolescent athlete
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Abstract Adolescence is a critical time for bone mass accrual, and increases in bone mass through puberty are dependent on rising levels
of gonadal steroids, growth hormone and insulin like growth factor-1. Many high school girls are involved in athletic activities,
and as many as 23.5% of adolescent athletes have been reported to develop amenorrhea. This review focuses on (1) factors that
determine which athletes are likely to develop amenorrhea, such as a negative energy balance state, low levels of leptin and
high levels of ghrelin, and (2) the impact of hypogonadism in athletes on bone metabolism. Benefi...
Source: Reviews in Endocrine & Metabolic Disorders - April 12, 2008 Category: Endocrinology Tags: Reviews in Endocrine & Metabolic Disorders Source Type: journals
Osteogenesis Imperfecta: Update on presentation and management
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Abstract Osteogenesis Imperfecta (OI) is a rare heritable condition characterized by bone fragility and reduced bone mass. Traditionally
OI was classified into OI types I to IV and thought to be only due to a defect in the collagen gene, however through the discovery
of the new types of OI–V to VII, breakthroughs have been made in understanding the pathophysiology of autosomal recessive
OI and new genetic mutations, such as in CRTAP and P3H1 genes. OI can present at any age and be difficult to diagnose because
of the wide phenotypic variation. Awareness of the new forms of OI, the differential diagnosis an...
Source: Reviews in Endocrine & Metabolic Disorders - April 11, 2008 Category: Endocrinology Tags: Reviews in Endocrine & Metabolic Disorders Source Type: journals
Inherited hypophosphatemic disorders in children and the evolving mechanisms of phosphate regulation
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Abstract Phosphorous is essential for multiple cellular functions and constitutes an important mineral in bone. Hypophosphatemia in
children leads to rickets resulting in abnormal growth and often skeletal deformities. Among various causes of low serum phosphorous
are inherited disorders associated with increased urinary excretion of phosphate, including autosomal dominant hypophosphatemic
rickets (ADHR), X-linked hypophosphatemia (XLH), autosomal recessive hypophosphatemia (ARHP), and hereditary hypophosphatemic
rickets with hypercalciuria (HHRH). Recent genetic analyses and subsequent biochemical and anima...
Source: Reviews in Endocrine & Metabolic Disorders - March 26, 2008 Category: Endocrinology Tags: Reviews in Endocrine & Metabolic Disorders Source Type: journals
Methods for measurement of pediatric bone
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Abstract Many experts believe that optimizing bone mineral accrual early in life may prevent childhood fractures and possibly delay
the development of osteoporosis later in life. Adequate nutrition and physical activity are environmental factors important
in determining whether or not children acquire an appropriate amount of bone for their body size. Pediatric diseases, or therapeutic
interventions used in their treatment, may interfere with normal bone development. Although there are specific methods available
for assessing pediatric bone, there is no one method that can adequately assess bone health and i...
Source: Reviews in Endocrine & Metabolic Disorders - February 5, 2008 Category: Endocrinology Tags: Reviews in Endocrine & Metabolic Disorders Source Type: journals
Celiac disease in children: Impact on bone health
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Abstract Celiac disease is a chronic enteropathy caused by permanent intolerance to gluten and similar proteins found in wheat, barley
and rye. The intestinal mucosa of susceptible individuals is crossed by undigested gluten, which leads to a marked inflammatory
response. The clinical features may vary from overt intestinal symptoms to silent disease. Bone health has been found to be
markedly affected in children and adolescents with untreated celiac disease, regardless of clinical presentation. Bone mass
measurements are greatly reduced compared to healthy youth. As indicated by surrogate markers of bone tu...
Source: Reviews in Endocrine & Metabolic Disorders - February 5, 2008 Category: Endocrinology Tags: Reviews in Endocrine & Metabolic Disorders Source Type: journals
