University of North Carolina at Chapel Hill School of Medicine, Chapel Hill, North Carolina; University of Alabama at Birmingham Heersink School of Medicine, Birmingham, Alabama; UTHealth Houston McGovern Medical School, Baylor College of Medicine, and Texas Children's Hospital, Houston, and University of Texas Medical Branch Galveston, Galveston, Texas; Columbia University Irving Medical Center, New York, New York; University of South Carolina School of Medicine Greenville/Prisma Health-Upstate, Greenville, South Carolina; University of California, San Diego, San Diego, California; University of Pennsylvania Perelman School of Medicine and Temple University Lewis Katz School of Medicine, Philadelphia, Pennsylvania; The Ohio State University College of Medicine and Wexner Medical Center, Columbus, Ohio; University of Mississippi Medical Center, Jackson, Mississippi; Indiana University School of Medicine Indianapolis, Indiana; Rutgers Health/Robert Wood Johnson Medical School, New Brunswick, New Jersey; Oregon Health & Science University Portland, Oregon; and Ochsner Health New Orleans, Louisiana.
Obstet Gynecol. 2024 Nov 1;144(5):733-739. doi: 10.1097/AOG.0000000000005720. Epub 2024 Sep 5.
To estimate the association between maternal metformin use for the treatment of early gestational or pre-existing type 2 diabetes and preterm preeclampsia.
This is a planned secondary analysis of the MOMPOD study (Medical Optimization of Management of Overt Type 2 Diabetes in Pregnancy), a randomized trial comparing the effect of adding metformin with insulin treatment on composite neonatal outcome in singleton pregnancies with early gestational or type 2 diabetes. Participants were randomized at 11-23 weeks of gestation to 1,000 mg metformin twice daily or placebo until delivery. A subset of participants had maternal blood collected at 24-30 weeks of gestation, and serum soluble endoglin, apolipoprotein B, vascular cell adhesion molecule-1, soluble fms-like tyrosine kinase 1, placental growth factor, high-sensitivity C-reactive protein, adiponectin, and vascular endothelial growth factor levels were measured. Our primary outcome was preterm preeclampsia , defined as preeclampsia requiring delivery before 37 weeks of gestation. Secondary outcomes included preterm preeclampsia requiring delivery before 34 weeks of gestation and differences in serum biomarkers. Multivariable regression analysis was used to estimate the associations between metformin use and primary or secondary study outcomes.
Of 831 participants, 119 (14.3%) developed preeclampsia requiring delivery before 37 weeks of gestation: 57 of 416 (13.7%) in the placebo group and 62 of 415 (14.9%) in the metformin group. Thirty-seven (4.4%) developed preeclampsia requiring delivery before 34 weeks of gestation: 15 (3.6%) receiving placebo and 22 (5.3%) receiving metformin. Compared with placebo, metformin was not associated with a significant difference in the occurrence of preeclampsia before 37 weeks of gestation (adjusted odds ratio [aOR] 1.04, 95% CI, 0.70-1.56) or before 34 weeks (aOR 1.43, 95% CI, 0.73-2.81). Similarly, there was no association between maternal metformin use and serum biomarker levels.
Among parturients with early gestational or pre-existing type 2 diabetes, the addition of metformin to insulin was not associated with lower odds of preterm preeclampsia or with serum biomarkers associated with cardiovascular disease risk.
评估早孕期或孕前 2 型糖尿病女性使用二甲双胍治疗与早产先兆子痫的相关性。
这是 MOMPOD 研究(妊娠显性 2 型糖尿病管理的医学优化)的一项计划中的二次分析,该研究是一项随机试验,比较了在早孕期或 2 型糖尿病的单胎妊娠中添加二甲双胍与胰岛素治疗对复合新生儿结局的影响。参与者在 11-23 孕周时随机分为每日两次口服 1000mg 二甲双胍组或安慰剂组,直至分娩。部分参与者在 24-30 孕周时采集了母亲的血液,并检测了血清可溶性内皮素、载脂蛋白 B、血管细胞黏附分子-1、可溶性 fms 样酪氨酸激酶 1、胎盘生长因子、高敏 C 反应蛋白、脂联素和血管内皮生长因子水平。我们的主要结局是早产先兆子痫,定义为需要在 37 孕周前分娩的子痫前期。次要结局包括需要在 34 孕周前分娩的早产先兆子痫和血清生物标志物的差异。多变量回归分析用于估计二甲双胍使用与主要或次要研究结局之间的关联。
在 831 名参与者中,119 名(14.3%)发生了需要在 37 孕周前分娩的子痫前期:安慰剂组 57 名(13.7%),二甲双胍组 62 名(14.9%)。37 名(4.4%)发生了需要在 34 孕周前分娩的子痫前期:安慰剂组 15 名(3.6%),二甲双胍组 22 名(5.3%)。与安慰剂相比,二甲双胍在 37 孕周前发生子痫前期的几率(校正优势比[aOR]1.04,95%CI,0.70-1.56)或 34 孕周前(aOR 1.43,95%CI,0.73-2.81)没有显著差异。同样,母亲使用二甲双胍与血清生物标志物水平之间也没有关联。
在早孕期或孕前 2 型糖尿病的产妇中,将二甲双胍添加到胰岛素中并不能降低早产先兆子痫的几率,也不能降低与心血管疾病风险相关的血清生物标志物水平。