Department of Medical Informatics and Clinical Epidemiology, School of Medicine, Oregon Health & Science University, Portland, Oregon.
School of Medicine, Oregon Health & Science University, Portland, Oregon.
JAMA Pediatr. 2014 Feb;168(2):178-84. doi: 10.1001/jamapediatrics.2013.4200.
Childhood obesity is an important public health problem with increasing prevalence. Because treatment often has limited success, new approaches must be identified.
To evaluate the effectiveness and safety of metformin for treating obesity in children aged 18 years and younger without a diagnosis of diabetes mellitus.
We included randomized clinical trials identified through searches of MEDLINE, the Cochrane Library, and ClinicalTrials.gov. Our primary outcome measure was change in body mass index (BMI, calculated as weight in kilograms divided by height in meters squared). We assessed study quality, pooled data using a random-effects model, and performed subgroup and sensitivity analyses.
Fourteen randomized clinical trials were eligible. For BMI, moderate-strength evidence indicated a reduction of -1.38 (95% CI, -1.93 to -0.82) from baseline compared with control at 6 months. A similar, if less dramatic, effect was observed in studies less than 6 months, but the pooled estimate from studies of 1 year of treatment was not statistically significant. Subgroup analyses indicated smaller, but significant, effects for those with baseline BMI below 35, those of Hispanic ethnicity, those with acanthosis nigricans, those who had tried and failed diet and exercise programs, and in studies with more girls or higher mean age (adolescents). Moderate-strength evidence indicated that with metformin, 26% reported a gastrointestinal event compared with 13% in control groups (relative risk, 2.05; 95% CI, 1.19-3.54), although there was no difference in discontinuations due to adverse events. No serious adverse events were reported.
Metformin provides a statistically significant, but very modest reduction in BMI when combined with lifestyle interventions over the short term. A large trial is needed to determine the benefits to subgroups or impacts of confounders. In the context of other options for treating childhood obesity, metformin has not been shown to be clinically superior.
儿童肥胖是一个日益严重的重要公共卫生问题。由于治疗往往收效甚微,因此必须找到新的方法。
评估二甲双胍治疗未被诊断为糖尿病的 18 岁及以下儿童肥胖的疗效和安全性。
我们通过检索 MEDLINE、Cochrane 图书馆和 ClinicalTrials.gov 纳入了随机临床试验。我们的主要结局指标是体重指数(BMI,体重以千克为单位,身高以米为单位)的变化。我们评估了研究质量,使用随机效应模型对数据进行了汇总,并进行了亚组和敏感性分析。
有 14 项随机临床试验符合条件。对于 BMI,与对照组相比,6 个月时基线值降低了 -1.38(95%置信区间,-1.93 至-0.82),这是中等强度的证据。在不到 6 个月的研究中观察到类似的效果,但治疗 1 年的研究中汇总的估计值没有统计学意义。亚组分析表明,对于基线 BMI 低于 35 的患者、西班牙裔患者、黑棘皮病患者、尝试过饮食和运动计划但失败的患者以及女孩或平均年龄较高的患者(青少年),效果较小但仍有显著意义。二甲双胍组有 26%的患者报告发生胃肠道事件,而对照组为 13%(相对风险,2.05;95%置信区间,1.19-3.54),但因不良事件停药的比例没有差异。未报告严重不良事件。
二甲双胍联合生活方式干预短期内可使 BMI 有统计学意义的但非常轻微的降低。需要进行大规模试验以确定对亚组的益处或混杂因素的影响。在治疗儿童肥胖的其他选择方面,二甲双胍尚未被证明在临床上具有优势。