Díaz Marta, Bassols Judit, López-Bermejo Abel, de Zegher Francis, Ibáñez Lourdes
Hospital Sant Joan de Déu, University of Barcelona, Esplugues, 08950, Spain.
Centro de Investigación Biomédica en Red de Diabetes y Enfermedades Metabólicas Asociadas (CIBERDEM), ISCIII, Madrid, Spain.
Pediatr Diabetes. 2015 Nov;16(7):538-45. doi: 10.1111/pedi.12220. Epub 2014 Oct 20.
Children born small-for-gestational-age (SGA) who experience rapid postnatal catch-up in weight are at risk for central adiposity and hyperinsulinemia.
To study the effects of prepubertal metformin intervention over 24 months on the body composition and endocrine-metabolic profile of catch-up SGA children.
Double-blind, placebo-controlled, pilot study including 23 post-catch-up non-obese prepubertal SGA children [age, 7.7 yr; body mass index standard deviation score (BMI SDS) >50th and <97th centile for age] with increased visceral fat [by magnetic resonance imaging (MRI) and insulin-like growth factor-I (IGF-I) both p > 75th for age]. Patients were randomized to receive either placebo or metformin (425 mg/d) for 24 months. Clinical, biochemical [IGF-I, glucose, insulin, lipids, androgens, sex-hormone-binding globulin (SHBG) and high-molecular-weight (HMW)-adiponectin] and imaging [body composition (absorptiometry and MRI; carotid intima-media thickness (ultrasonography)] variables were assessed at baseline, and at 6, 12, and 24 months.
After 24 months, metformin-treated children were leaner, had higher SHBG levels, and less total and abdominal fat than placebo-treated children (all p ≤ 0.05). Longitudinal analyses showed that metformin had a significant effect on anthropometric (weight, BMI, and waist) and biochemical variables [glucose, homeostasis model assessment-insulin resistance (HOMA-IR), and triglycerides] (all p ≤ 0.05); and in total and abdominal fat (p = 0.01 and p = 0.02).
Prepubertal intervention with metformin reduces central adiposity and improves insulin sensitivity in non-obese catch-up SGA children.
出生时小于胎龄(SGA)的儿童,若出生后体重快速追赶生长,则有发生中心性肥胖和高胰岛素血症的风险。
研究青春期前24个月二甲双胍干预对追赶生长的SGA儿童身体成分和内分泌代谢状况的影响。
双盲、安慰剂对照的前瞻性研究,纳入23名追赶生长的青春期前非肥胖SGA儿童[年龄7.7岁;体重指数标准差评分(BMI SDS)处于年龄别第50至第97百分位数之间],其内脏脂肪增加[通过磁共振成像(MRI)检查,且胰岛素样生长因子-I(IGF-I)均处于年龄别第75百分位数以上]。患者被随机分为两组,分别接受安慰剂或二甲双胍(425mg/d)治疗24个月。在基线、6个月、12个月和24个月时评估临床、生化指标[IGF-I、葡萄糖、胰岛素、血脂、雄激素、性激素结合球蛋白(SHBG)和高分子量(HMW)脂联素]以及影像学指标[身体成分(双能X线吸收法和MRI);颈动脉内膜中层厚度(超声检查)]。
24个月后,与接受安慰剂治疗的儿童相比,接受二甲双胍治疗的儿童更瘦,SHBG水平更高,总脂肪和腹部脂肪更少(所有p≤0.05)。纵向分析显示,二甲双胍对人体测量学指标(体重、BMI和腰围)和生化指标[葡萄糖、稳态模型评估胰岛素抵抗(HOMA-IR)和甘油三酯]有显著影响(所有p≤0.05);对总脂肪和腹部脂肪也有显著影响(p=0.01和p=0.02)。
青春期前使用二甲双胍进行干预可减少非肥胖追赶生长SGA儿童的中心性肥胖,并改善其胰岛素敏感性。