Discipline of Obstetrics & Gynaecology and Robinson Research Institute, University of Adelaide, Adelaide, SA, Australia; Department of Perinatal Medicine, Women's and Children's Hospital, North Adelaide, SA, Australia.
Discipline of Obstetrics & Gynaecology and Robinson Research Institute, University of Adelaide, Adelaide, SA, Australia; School of Public Health, University of Adelaide, Adelaide, SA, Australia.
Lancet Diabetes Endocrinol. 2019 Jan;7(1):15-24. doi: 10.1016/S2213-8587(18)30310-3. Epub 2018 Dec 4.
Maternal overweight and obesity are associated with well recognised pregnancy complications. Antenatal dietary and lifestyle interventions have a modest effect on gestational weight gain without affecting pregnancy outcomes. We aimed to assess the effects on maternal and infant outcomes of antenatal metformin given in addition to dietary and lifestyle advice among overweight and obese pregnant women.
GRoW was a multicentre, randomised, double-blind, placebo-controlled trial in which pregnant women at 10-20 weeks' gestation with a BMI of 25 kg/m or higher were recruited from three public maternity units in Adelaide, SA, Australia. Women were randomly assigned (1:1) via a computer-generated schedule to receive either metformin (to a maximum dose of 2000 mg per day) or matching placebo. Participants, their antenatal care providers, and research staff (including outcome assessors) were masked to treatment allocation. All women received an antenatal dietary and lifestyle intervention. The primary outcome was the proportion of infants with birthweight greater than 4000 g. Secondary outcomes included measures of maternal weight gain, maternal diet and physical activity, maternal pregnancy and birth outcomes, maternal quality of life and emotional wellbeing, and infant birth outcomes. Outcomes were analysed on an intention-to-treat basis (including all randomly assigned women who did not withdraw consent to use their data, and who did not have a miscarriage or termination of pregnancy before 20 weeks' gestation, or a stillbirth). The trial is registered with the Australian New Zealand Clinical Trials Registry, number ACTRN12612001277831.
Of 524 women who were randomly assigned between May, 28 2013 and April 26, 2016, 514 were included in outcome analyses (256 in the metformin group and 258 in the placebo group). Median gestational age at trial entry was 16·29 weeks (IQR 14·43-18·00) and median BMI was 32·32 kg/m (28·90-37·10); 167 (32%) participants were overweight and 347 (68%) were obese. There was no significant difference in the proportion of infants with birthweight greater than 4000 g (40 [16%] with metformin vs 37 [14%] with placebo; adjusted risk ratio [aRR] 0·97, 95% CI 0·65 to 1·47; p=0·899). Women receiving metformin had lower average weekly gestational weight gain (adjusted mean difference -0·08 kg, 95% CI -0·14 to -0·02; p=0·007) and were more likely to have gestational weight gain below recommendations (aRR 1·46, 95% CI 1·10 to 1·94; p=0·008). Total gestational weight gain, pregnancy and birth outcomes, maternal diet and physical activity, and maternal quality of life and emotional wellbeing did not differ significantly between groups. Similar numbers of women in both treatment groups (76% [159/208] in the metformin group and 73% [144/196] in the placebo group) reported side-effects including nausea, diarrhoea, and vomiting. Two stillbirths (placebo group) and one neonatal death (metformin group) occurred; none of the perinatal deaths were determined to be attributable to participation in the trial.
For pregnant women who are overweight or obese, metformin given in addition to dietary and lifestyle advice initiated at 10-20 weeks' gestation does not improve pregnancy and birth outcomes.
Australian National Health and Medical Research Council.
母亲超重和肥胖与公认的妊娠并发症有关。产前饮食和生活方式干预对妊娠体重增加有一定的影响,但不会影响妊娠结局。我们旨在评估在超重和肥胖孕妇中,除了饮食和生活方式建议外,在 10-20 周妊娠时给予产前二甲双胍对母婴结局的影响。
GRoW 是一项多中心、随机、双盲、安慰剂对照试验,在澳大利亚阿德莱德的三个公立产科单位招募了 BMI 为 25kg/m 或更高的 10-20 周妊娠的孕妇。妇女通过计算机生成的时间表以 1:1 的比例随机分配接受二甲双胍(最大剂量为每天 2000mg)或匹配的安慰剂。参与者、他们的产前保健提供者和研究人员(包括结局评估者)对治疗分配进行了盲法。所有妇女都接受了产前饮食和生活方式干预。主要结局是出生体重大于 4000g 的婴儿比例。次要结局包括测量产妇体重增加、产妇饮食和身体活动、产妇妊娠和分娩结局、产妇生活质量和情绪健康、以及婴儿分娩结局。分析结果采用意向治疗(包括所有未退出同意使用其数据的随机分配妇女,以及在 20 周妊娠前无流产或终止妊娠、或死产的妇女)。该试验在澳大利亚和新西兰临床试验注册中心注册,编号为 ACTRN12612001277831。
在 2013 年 5 月 28 日至 2016 年 4 月 26 日期间随机分配的 524 名妇女中,有 514 名妇女纳入结局分析(二甲双胍组 256 名,安慰剂组 258 名)。试验入组时的中位妊娠年龄为 16.29 周(IQR 14.43-18.00),中位 BMI 为 32.32kg/m(28.90-37.10);167(32%)名参与者超重,347(68%)名参与者肥胖。出生体重大于 4000g 的婴儿比例无显著差异(二甲双胍组 40 名[16%],安慰剂组 37 名[14%];调整风险比[aRR]0.97,95%CI 0.65 至 1.47;p=0.899)。接受二甲双胍的妇女每周平均妊娠体重增加较少(调整平均差异-0.08kg,95%CI-0.14 至-0.02;p=0.007),更有可能体重增加低于建议(调整比值比[aRR]1.46,95%CI 1.10 至 1.94;p=0.008)。两组的总妊娠体重增加、妊娠和分娩结局、产妇饮食和身体活动以及产妇生活质量和情绪健康无显著差异。两组中相似数量的妇女(二甲双胍组 76%[159/208],安慰剂组 73%[144/196])报告了包括恶心、腹泻和呕吐在内的副作用。两组各有一例死产(安慰剂组)和一例新生儿死亡(二甲双胍组);没有一例围产期死亡被确定与参与试验有关。
对于超重或肥胖的孕妇,在 10-20 周妊娠时除了饮食和生活方式建议外,给予二甲双胍并不能改善妊娠和分娩结局。
澳大利亚国家卫生和医学研究委员会。