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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    European journal of pediatrics 148 (1988), S. 233-237 
    ISSN: 1432-1076
    Keywords: Insulin and C-peptide ; Metabolism ; Receptor ; Obesity ; Weight loss
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract To study the relationship between childhood obesity, weight loss, hyperinsulinaemia and the erythrocyte insulin receptor, we measured the plasma concentrations of immunoreactive insulin (IRI) and C-peptide and the binding of 125I-insulin to erythrocytes in 12 obese children with a mean age ±SD of 11.4±2.5 years and a mean relative weight score ±SD of 4.8±1.4 and 12 age-matched normal-weight children. Eight obese children were re-evaluated after 1 year's participation in a weight reduction programme. The obese children had higher fasting plasma concentrations of IRI (P〈0.01) and C-peptide (P〈0.05) and a lower C-peptide to IRI molar ratio (P〈0.01) than the normal-weight children. The obese children had in addition a reduced erythrocyte insulin binding (P〈0.05 or less) over the physiological range of circulating insulin concentration. There was a negative correlation (r=−0.60; P〈0.01) between the insulin tracer binding and the relative weight. The weight reduction programme resulted in a decrease of 1.0SD (P〈0.05) in the mean relative weight score. At the end of the therapy the obese children had lower fasting blood glucose levels (P〈0.05) and lower plasma IRI concentrations at 90 min (P〈0.05) after an oral glucose load than at the onset of therapy. There were no significant differences between the insulin binding characteristics at the commencement and at the end of the treatment. The low C-peptide to IRI molar ratio in obese children provides evidence of a decreased insulin clearance likely to contribute to their hyperinsulinaemia. The inverse relationship between insulin tracer binding and relative weight suggests a mechanism by which weight changes may be directly reflected in the peripheral insulin sensitivity. A moderate weight loss reduces hyperinsulinaemia in childhood obesity but does not normalize the impaired binding of insulin to its receptor.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular medicine 66 (1988), S. 216-222 
    ISSN: 1432-1440
    Keywords: Fat distribution ; Hyperinsulinemia ; Obesity ; Glucose tolerance ; Non-insulin dependent diabetes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Relationship between body fat distribution, serum insulin, and glucose tolerance in obese, non-diabetic women. Recent studies suggest that hyperinsulinemia and upper body obesity are predictive factors for the development of non-insulindependent diabetes mellitus. To further characterize the relationship between body fat distribution, serum insulin, and glucose tolerance an oral glucose tolerance test was performed in 48 obese, nondiabetic women. Fasting insulin levels were correlated to both total body fat calculated as body mass index (r=0.58,p〈0.001) and upper body fat distribution expressed as waist-to-hip ratio (WHR,r=0.47,p〈0.01). In the women with upper body fat localization (WHR〉0.90) significantly higher basal and glucose-stimulated insulin concentrations were established than in the women with a lower body type of obesity (WHR〈0.78) (basal insulin 27.4±11.5 vs. 15.4±8.8 mU/l,p〈0.05, insulin area 779±320 vs. 468±237 U,p〈0.05). They also had impaired glucose tolerance (glucose area 925±139 vs. 633±147 U,p〈0.01). Fasting triglyceride concentrations were correlated both with WHR (r=0.63,p〈0.001) and fasting insulin (r=0.33,p〈0.05) but not with BMI (r=−0.02, n.s.). A positive association was found between systolic and diastolic blood pressure and both WHR (r=0.43 andr=0.44 resp.,p〈0.01) and BMI (eachr=0.35,p〈0.05). Interestingly, basal insulin was also associated with blood pressure (r=0.30,p〈0.1, andr=0.40,p〈0.01 resp.). These results suggest a close relationship between upper body obesity, hyperinsulinemia, and impaired glucose tolerance. Women with an upper body tpye of obesity also show tendencies to hypertriglyceridemia and hypertension. Obese women with upper body obesity represent a subgroup of the obesity population with an increased risk to develop type-II diabetes.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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