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Randomized, controlled trial of metformin for obesity and insulin resistance in children and adolescents: improvement in body composition and fasting insulin
Authors:Srinivasan Shubha  Ambler Geoffrey R  Baur Louise A  Garnett Sarah P  Tepsa Mirijana  Yap Fabian  Ward Glenn M  Cowell Christopher T
Affiliation:Institute of Endocrinology and Diabetes, The Children's Hospital at Westmead, Locked Bag 4001 Westmead, New South Wales 2145, Australia. shubhas@chw.edu.au
Abstract:CONTEXT: Metformin therapy for adults and children with type 2 diabetes is well established. However, its role in the treatment of insulin resistance and obesity in children and adolescents is less clearly defined. OBJECTIVE: We assessed the effect of metformin on body composition and insulin sensitivity in pediatric subjects with exogenous obesity. DESIGN AND SETTING: Patients referred to a pediatric endocrine clinic were enrolled in a randomized, double-blind, crossover trial. PATIENTS: Twenty-eight patients (13 males) aged 9-18 yr participated in the study. INTERVENTION: Patients received metformin (1 g twice daily) and placebo for 6 months, each with a 2-wk washout period. MAIN OUTCOME MEASURES: Body composition (anthropometry, dual-energy x-ray absorptiometry, and abdominal magnetic resonance imaging), and insulin sensitivity (Si; minimal model, fasting insulin and glucose) were measured at baseline and 6 and 12 months. RESULTS: Mean age of subjects at baseline was 12.5 +/- 2.2 yr, median body mass index z-score 2.54 (range, 1.93-2.85). Metformin had a greater treatment effect over placebo for weight (-4.35 kg, P = 0.02), body mass index (-1.26 kg/m(2), P = 0.002), waist circumference (-2.8 cm, P = 0.003), sc abdominal adipose tissue (-52.5 cm(2), P = 0.002), and fasting insulin (-2.2 mU/liter, P = 0.011). Si improved in 45% of subjects while on metformin and 27% of subjects while on placebo (P = 0.21). CONCLUSIONS: Metformin therapy for obese insulin-resistant pediatric patients results in significant improvement in body composition and fasting insulin. Although improvement in Si was noted in many individuals, Si was a less useful parameter for analysis of group data, possibly because of effects of variable compliance and changing Si during puberty.
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