Juuma Elina, Tihtonen Kati, Metso Saara E, Hannula Päivi M, Helminen Mika, Tertti Kristiina, Immonen Heidi, Georgiadis Leena, Väyrynen Kirsi, Ahtiainen Petteri, Nikkinen Hilkka, Koivikko Minna, Laivuori Hannele, Uotila Jukka
Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.
Department of Obstetrics and Gynecology, Wellbeing Services County of Central Finland, Jyväskylä, Finland.
Diabetes Metab Res Rev. 2025 Sep;41(6):e70085. doi: 10.1002/dmrr.70085.
Our aim was to ascertain whether metformin can reduce insulin requirement without compromising glycaemic control during pregnancy in women with type 1 diabetes.
A total of 126 pregnant women with type 1 diabetes were recruited for a randomised, double-blind, placebo-controlled multicentre study. The primary outcome was total insulin change, defined as the difference between baseline and third trimester maximum insulin dose (IU).
Fifty women in the placebo group and 51 women in the metformin group completed the study. A predetermined sample size of 200 participants was not achieved. There was no significant difference in the primary outcome, that is, in the change of total insulin requirement (33 vs. 27 IU, p = 0.193). However, the metformin group showed a significantly lower increase in the prandial insulin change, with 24 versus 14 IU (p = 0.014) and 0.3 versus 0.2 IU/kg (p = 0.048). In the exploratory subgroup analysis, metformin attenuated prandial insulin increase in women with high BMI (> 25 kg/m) or high baseline insulin requirement (> 40 IU) (25 vs. 15 IU, p = 0.028, 30 vs. 14 IU, p = 0.007). Weight gain remained more often within target in the metformin group (20% vs. 40%, p = 0.029). A similar weight benefit was observed in subgroups (BMI> 25 kg/m 8% vs. 32%, p = 0.005, insulin requirement> 40 IU 6% vs. 34%, p = 0.004). No differences were seen in glycaemic control or neonatal outcome between the groups.
Metformin was not shown to affect total insulin change but reduced the prandial insulin change and improved weight gain control especially in insulin-resistant subgroups. These findings warrant further studies on metformin as an adjunctive medicine.
ClinicalTrials.gov: NCT03765359.
我们的目的是确定二甲双胍是否能在不影响1型糖尿病孕妇血糖控制的情况下减少胰岛素需求量。
总共招募了126名1型糖尿病孕妇参与一项随机、双盲、安慰剂对照的多中心研究。主要结局是总胰岛素变化,定义为基线与孕晚期最大胰岛素剂量(国际单位)之间的差值。
安慰剂组50名女性和二甲双胍组51名女性完成了研究。未达到预定的200名参与者的样本量。主要结局,即总胰岛素需求量的变化,无显著差异(33对27国际单位,p = 0.193)。然而,二甲双胍组餐时胰岛素变化的增加显著更低,分别为24对14国际单位(p = 0.014)以及0.3对0.2国际单位/千克(p = 0.048)。在探索性亚组分析中,二甲双胍减轻了高体重指数(>25千克/米²)或高基线胰岛素需求量(>40国际单位)女性的餐时胰岛素增加(25对15国际单位,p = 0.028,30对14国际单位,p = 0.007)。二甲双胍组体重增加更常保持在目标范围内(20%对40%,p = 0.029)。在亚组中也观察到了类似的体重益处(体重指数>25千克/米² 8%对32%,p = 0.005,胰岛素需求量>40国际单位6%对34%,p = 0.004)。两组之间在血糖控制或新生儿结局方面未见差异。
未显示二甲双胍会影响总胰岛素变化,但减少了餐时胰岛素变化,并改善了体重增加控制,尤其是在胰岛素抵抗亚组中。这些发现值得对二甲双胍作为辅助药物进行进一步研究。
ClinicalTrials.gov:NCT03765359。