Worsley R, Jane F, Robinson P J, Bell R J, Davis S R
Women's Health Research Program, School of Public Health and Preventive Medicine, Department of Epidemiology and Preventive Medicine, Monash University , Melbourne, Victoria , Australia.
Climacteric. 2015 Apr;18(2):270-7. doi: 10.3109/13697137.2014.954997. Epub 2014 Oct 21.
This study was undertaken to determine whether metformin would ameliorate insulin resistance, reduce weight and waist circumference and improve lipids in obese, but not morbidly obese, euglycemic women.
Obese women (body mass index (BMI) ≥ 30 and < 40 kg/m(2) and/or waist circumference > 88 cm), aged 35-65 were randomized (1:1) to metformin 850 mg or identical placebo, twice daily for 26 weeks. The primary outcome was the change in insulin resistance determined by the homeostasis model of assessment (HOMA-IR). Secondary outcomes included fasting insulin, glucose, weight, waist circumference and BMI.
Of the 125 women screened, 117 enrolled and 100 women, mean age 53 years, were included in the primary intention-to-treat analysis. Metformin resulted in statistically significant between-group difference in the change in HOMA-IR (change in median - 0.04 vs. placebo + 0.1, p = 0.018) and BMI (mean change - 1.00 kg/m(2); 95% confidence interval (CI) 1.37 to - 0.62 vs. placebo mean change 0.00; 95% CI - 0.29 to 0.28, p < 0.001). Statistically significant reductions in HbA1c (p = 0.008) and fasting insulin (p = 0.03) and a borderline decrease in high density lipoprotein cholesterol (p = 0.07) were also observed for metformin, compared with placebo. No effects were seen for waist circumference, fasting glucose or other lipids.
Treatment of euglycemic, obese, middle-aged women with metformin 1700 mg per day reduced insulin resistance and weight compared with placebo. Further studies are needed to determine whether the use of metformin will prevent the progression of insulin resistance to type 2 diabetes mellitus in obese women.
本研究旨在确定二甲双胍是否能改善肥胖但非病态肥胖的血糖正常女性的胰岛素抵抗、减轻体重和腰围并改善血脂。
年龄在35 - 65岁的肥胖女性(体重指数(BMI)≥30且<40 kg/m²和/或腰围>88 cm)被随机(1:1)分为二甲双胍850 mg组或相同安慰剂组,每日两次,共26周。主要结局是通过稳态模型评估(HOMA-IR)确定的胰岛素抵抗变化。次要结局包括空腹胰岛素、血糖、体重、腰围和BMI。
在125名筛查的女性中,117名入选,100名平均年龄53岁的女性被纳入主要意向性治疗分析。二甲双胍导致组间HOMA-IR变化(中位数变化 -0.04 vs. 安慰剂 +0.1,p = 0.018)和BMI(平均变化 -1.00 kg/m²;95%置信区间(CI)-1.37至 -0.62 vs. 安慰剂平均变化0.00;95% CI -0.29至0.28,p < 0.001)有统计学显著差异。与安慰剂相比,二甲双胍还观察到HbA1c(p = 0.008)和空腹胰岛素(p = 0.03)有统计学显著降低,高密度脂蛋白胆固醇有临界性降低(p = 0.07)。腰围、空腹血糖或其他血脂未见影响。
与安慰剂相比,每天用1700 mg二甲双胍治疗血糖正常的肥胖中年女性可降低胰岛素抵抗和体重。需要进一步研究以确定二甲双胍的使用是否能预防肥胖女性胰岛素抵抗进展为2型糖尿病。