Dunne Fidelma, Newman Christine, Alvarez-Iglesias Alberto, O'Shea Paula, Devane Declan, Gillespie Paddy, Egan Aoife, O'Donnell Martin, Smyth Andrew
Institute for Clinical Trials, College of Medicine, Nursing and Health Sciences, University of Galway, Galway H91 TK33, Ireland.
HRB Clinical Research Facility Galway, University of Galway, Galway H91 TK33, Ireland.
J Clin Endocrinol Metab. 2025 Apr 22;110(5):e1566-e1572. doi: 10.1210/clinem/dgae522.
Women with gestational diabetes mellitus (GDM) display adverse lifetime cardiometabolic health. We examined whether early metformin in GDM could impact cardiometabolic risk factors postpartum.
EMERGE, a double-blind, placebo-controlled trial, randomized pregnancies 1:1 to placebo or metformin at GDM diagnosis and followed participants from randomization until 12 ± 4 weeks postpartum. In total, 478 pregnancies were available for postpartum maternal assessment, 237 and 241 assigned to metformin and placebo respectively. Weight (kg), body mass index (BMI) (kg/m2), waist circumference (cm), and blood pressure (mmHg) were measured, infant feeding method documented, and blood specimens drawn for a 75-gram oral glucose tolerance test, fasting insulin, C-peptide, and lipid analysis.
Despite similar weight and BMI at trial randomization, participants receiving metformin had significantly lower weight (79.5 ± 15.9 vs 82.6 ± 16.9 kg; P = .04) and BMI (29.3 [5.6] vs 30.5 [5.4]; P = .018) at the postpartum visit. However, no difference in weight change from randomization to 12 weeks postpartum was observed between metformin and placebo groups. Overall, 29% (n = 139) of the cohort met criteria for prediabetes or diabetes, with no positive impact with metformin. There were also no differences in measurements of insulin resistance, blood pressure, or lipids between groups.
Early metformin use in GDM did not impact important cardiometabolic parameters in the early postpartum period despite significant benefits in weight gain and insulin use in pregnancy.
患有妊娠期糖尿病(GDM)的女性存在不良的终生心脏代谢健康问题。我们研究了妊娠期糖尿病患者早期使用二甲双胍是否会影响产后心脏代谢危险因素。
EMERGE是一项双盲、安慰剂对照试验,在妊娠期糖尿病诊断时将孕妇按1:1随机分为安慰剂组或二甲双胍组,并从随机分组开始跟踪参与者直至产后12±4周。共有478例妊娠可用于产后母亲评估,分别有237例和241例被分配到二甲双胍组和安慰剂组。测量体重(kg)、体重指数(BMI)(kg/m²)、腰围(cm)和血压(mmHg),记录婴儿喂养方式,并采集血样进行75克口服葡萄糖耐量试验、空腹胰岛素、C肽和血脂分析。
尽管在试验随机分组时体重和BMI相似,但接受二甲双胍治疗的参与者在产后访视时体重(79.5±15.9 vs 82.6±16.9 kg;P = 0.04)和BMI(29.3[5.6] vs 30.5[5.4];P = 0.018)显著较低。然而,二甲双胍组和安慰剂组从随机分组到产后12周的体重变化没有差异。总体而言,该队列中有29%(n = 139)符合糖尿病前期或糖尿病标准,二甲双胍对其没有积极影响。两组之间在胰岛素抵抗、血压或血脂测量方面也没有差异。
妊娠期糖尿病早期使用二甲双胍对产后早期的重要心脏代谢参数没有影响,尽管在孕期体重增加和胰岛素使用方面有显著益处。