First Department of Obstetrics and Gynecology, Alexandra Hospital, National and Kapodistrian University of Athens, Athens, Greece.
Arch Gynecol Obstet. 2024 Oct;310(4):1895-1903. doi: 10.1007/s00404-024-07618-8. Epub 2024 Aug 14.
Myo-inositol (MI) is an insulin-sensitizing dietary supplement, enhancing the transfer of glucose into the cell. Gestational diabetes mellitus (GDM) is characterized by abnormal glucose tolerance, which is associated with elevated insulin resistance. The present study aimed to assess the effect of MI supplementation during pregnancy on the incidence of GDM.
We performed a single-center, open-label, randomized controlled trial. A cohort of 200 pregnant women at 11-13 weeks of gestation were randomly assigned in two groups: MI group (n = 100) and control group (n = 100). The MI group received MI and folic acid (4000 mg MI and 400 mcg folic acid daily), while the control group received folic acid alone (400 mcg folic acid daily) until 26-28 weeks of gestation, when the 75 g Oral Glucose Tolerance Test (OGTT) was performed for the diagnosis of GDM. Clinical and metabolic outcomes were assessed.
The incidence of GDM was significantly higher in the MI group (14.9%) compared to the control group (28.5%) (P = 0.024). Women treated with MI had significantly lower OGTT glucose values, than those not treated with MI (P < 0.001). The insulin resistance as assessed by HOMA-IR was significantly lower in the MI group versus control (P = 0.045). Furthermore, MI group had significantly higher insulin sensitivity as measured by the Matsuda Index, compared to the control group (P = 0.037).
MI supplementation seems to be an effective option to improve the glycemic control of pregnant women and prevent the onset of GDM.
ISRCTN registry: ISRCTN16142533. Registered 09 March 2017.
肌醇(MI)是一种胰岛素增敏膳食补充剂,可增强葡萄糖向细胞内的转运。妊娠糖尿病(GDM)的特征是葡萄糖耐量异常,与胰岛素抵抗升高有关。本研究旨在评估妊娠期间 MI 补充对 GDM 发生率的影响。
我们进行了一项单中心、开放标签、随机对照试验。将 200 名 11-13 周妊娠的孕妇分为两组:MI 组(n=100)和对照组(n=100)。MI 组接受 MI 和叶酸(4000 mg MI 和 400 mcg 叶酸每天),对照组仅接受叶酸(每天 400 mcg 叶酸),直至 26-28 周,此时进行 75 g 口服葡萄糖耐量试验(OGTT)以诊断 GDM。评估临床和代谢结局。
MI 组 GDM 的发生率明显高于对照组(14.9%比 28.5%,P=0.024)。接受 MI 治疗的女性 OGTT 血糖值明显低于未接受 MI 治疗的女性(P<0.001)。MI 组的 HOMA-IR 评估的胰岛素抵抗明显低于对照组(P=0.045)。此外,与对照组相比,MI 组的 Matsuda 指数评估的胰岛素敏感性明显更高(P=0.037)。
MI 补充似乎是改善孕妇血糖控制并预防 GDM 发生的有效选择。
ISRCTN 注册处:ISRCTN84246732。2017 年 3 月 9 日注册。