University of North Carolina at Chapel Hill School of Medicine.
University of North Carolina Gillings School of Global Public Health Chapel Hill.
JAMA. 2023 Dec 12;330(22):2182-2190. doi: 10.1001/jama.2023.22949.
Insulin is recommended for pregnant persons with preexisting type 2 diabetes or diabetes diagnosed early in pregnancy. The addition of metformin to insulin may improve neonatal outcomes.
To estimate the effect of metformin added to insulin for preexisting type 2 or diabetes diagnosed early in pregnancy on a composite adverse neonatal outcome.
DESIGN, SETTING, AND PARTICIPANTS: This randomized clinical trial in 17 US centers enrolled pregnant adults aged 18 to 45 years with preexisting type 2 diabetes or diabetes diagnosed prior to 23 weeks' gestation between April 2019 and November 2021. Each participant was treated with insulin and was assigned to add either metformin or placebo. Follow-up was completed in May 2022.
Metformin 1000 mg or placebo orally twice per day from enrollment (11 weeks -<23 weeks) through delivery.
The primary outcome was a composite of neonatal complications including perinatal death, preterm birth, large or small for gestational age, and hyperbilirubinemia requiring phototherapy. Prespecified secondary outcomes included maternal hypoglycemia and neonatal fat mass at birth, and prespecified subgroup analyses by maternal body mass index less than 30 vs 30 or greater and those with preexisting vs diabetes early in pregnancy.
Of the 831 participants randomized, 794 took at least 1 dose of the study agent and were included in the primary analysis (397 in the placebo group and 397 in the metformin group). Participants' mean (SD) age was 32.9 (5.6) years; 234 (29%) were Black, and 412 (52%) were Hispanic. The composite adverse neonatal outcome occurred in 280 (71%) of the metformin group and in 292 (74%) of the placebo group (adjusted odds ratio, 0.86 [95% CI 0.63-1.19]). The most commonly occurring events in the primary outcome in both groups were preterm birth, neonatal hypoglycemia, and delivery of a large-for-gestational-age infant. The study was halted at 75% accrual for futility in detecting a significant difference in the primary outcome. Prespecified secondary outcomes and subgroup analyses were similar between groups. Of individual components of the composite adverse neonatal outcome, metformin-exposed neonates had lower odds to be large for gestational age (adjusted odds ratio, 0.63 [95% CI, 0.46-0.86]) when compared with the placebo group.
Using metformin plus insulin to treat preexisting type 2 or gestational diabetes diagnosed early in pregnancy did not reduce a composite neonatal adverse outcome. The effect of reduction in odds of a large-for-gestational-age infant observed after adding metformin to insulin warrants further investigation.
ClinicalTrials.gov Identifier: NCT02932475.
胰岛素被推荐用于患有 2 型糖尿病或在妊娠早期诊断出的糖尿病的孕妇。将二甲双胍添加到胰岛素中可能会改善新生儿结局。
评估在患有 2 型糖尿病或在妊娠 23 周前诊断出的糖尿病的孕妇中,添加二甲双胍到胰岛素治疗方案中对复合不良新生儿结局的影响。
设计、地点和参与者:这项在 17 个美国中心进行的随机临床试验纳入了年龄在 18 至 45 岁之间的患有 2 型糖尿病或在妊娠 23 周前诊断出的糖尿病的孕妇。每位参与者均接受胰岛素治疗,并被分配添加二甲双胍或安慰剂。随访于 2022 年 5 月完成。
从入组(11 周到<23 周)到分娩,每天口服两次二甲双胍 1000mg 或安慰剂。
主要结局是新生儿并发症的综合指标,包括围产期死亡、早产、大于或小于胎龄儿和需要光疗的高胆红素血症。预先指定的次要结局包括产妇低血糖和新生儿出生时的脂肪量,以及按产妇体重指数(BMI)<30 与≥30 和妊娠前 vs 妊娠早期糖尿病进行的预先指定亚组分析。
在 831 名随机参与者中,794 名至少服用了 1 剂研究药物,并纳入了主要分析(安慰剂组 397 名,二甲双胍组 397 名)。参与者的平均(SD)年龄为 32.9(5.6)岁;234 名(29%)为黑人,412 名(52%)为西班牙裔。在二甲双胍组中,复合不良新生儿结局发生在 280 名(71%)参与者中,在安慰剂组中发生在 292 名(74%)参与者中(调整后的优势比,0.86[95%CI,0.63-1.19])。两组中主要结局中最常见的事件是早产、新生儿低血糖和分娩出大于胎龄儿。该研究在达到 75%的入组人数后,因无法检测到主要结局的显著差异而停止。次要结局和亚组分析与各组之间的预先指定结果相似。与安慰剂组相比,接受二甲双胍治疗的新生儿发生大于胎龄儿的几率较低(调整后的优势比,0.63[95%CI,0.46-0.86])。
使用二甲双胍加胰岛素治疗妊娠前或妊娠早期诊断出的 2 型糖尿病并不能降低复合新生儿不良结局的风险。在胰岛素中添加二甲双胍后观察到的降低大于胎龄儿几率的效果需要进一步研究。
ClinicalTrials.gov 标识符:NCT02932475。