Bertrand Anthéa, Gallot Denis, Pereira Bruno, Delabaere Amélie
CHU Clermont-Ferrand, Pôle Femme Et Enfant, 1 Place Lucie et Raymond Aubrac 63003 CLERMONT-FERRAND Cedex 1, France.
Equipe, "Translationnal Approach to Epithelial Injury and Repair", Université Clermont Auvergne, CNRS, Inserm, GReD, F-63000, Clermont-Ferrand, France.
Curr Res Pharmacol Drug Discov. 2022 Nov 22;4:100140. doi: 10.1016/j.crphar.2022.100140. eCollection 2023.
Gestational diabetes (GD) is associated with an increase in maternal and fetal morbidity. The risk factors involved have been clearly identified but no prevention strategies have yet provided robust evidence of their efficacy. Myoinositol has insulin sensitization properties and is of potential interest in the treatment of the disorder.
The aim of this work was to assess the efficacy of myoinositol supplementation during pregnancy to prevent GD in patients with known risk factors.
A systematic literature review was performed on studies comparing the effects of myoinositol supplementation and placebo on the occurrence of GD in at-risk pregnant women. The main judgement criterion was diagnosis of GD between 24 and 28 gestational weeks by an oral glucose tolerance test. The secondary judgement criteria were the occurrence of maternal fetal complications and the need to initiate insulin treatment to manage GD.
Nine studies were included in the meta-analysis. The results showed a significantly higher risk of GD in patients on placebo than in those receiving myoinositol (RR = 2.58, CI 95%: 1.68 to 3.97, p < 0.0001) but wide variations between studies (I = 71.94%, p < 0.001). And the risk of prematurity was significantly greater in the children of mothers on placebo (RR: 2.15, IC 95%: 1.32 to 3.20, p = 0.002).
Myoinositol supplementation taken from the beginning of pregnancy reduces the incidence of GD and could be of interest at a dose of 4 g/day as a prevention strategy for patients with identified risk factors.
妊娠期糖尿病(GD)与母婴发病率增加有关。相关危险因素已明确,但尚无预防策略能提供有力的疗效证据。肌醇具有胰岛素增敏特性,在该疾病治疗中具有潜在价值。
本研究旨在评估孕期补充肌醇对有已知危险因素的患者预防妊娠期糖尿病的疗效。
对比较肌醇补充剂和安慰剂对高危孕妇妊娠期糖尿病发生影响的研究进行系统文献综述。主要判断标准为通过口服葡萄糖耐量试验在孕24至28周诊断出妊娠期糖尿病。次要判断标准为母婴并发症的发生情况以及启动胰岛素治疗来控制妊娠期糖尿病的必要性。
九项研究纳入荟萃分析。结果显示,服用安慰剂的患者患妊娠期糖尿病的风险显著高于服用肌醇的患者(相对危险度[RR]=2.58,95%置信区间[CI]:1.68至3.97,p<0.0001),但各研究间差异较大(异质性检验I=71.94%,p<0.001)。并且,服用安慰剂母亲的孩子早产风险显著更高(RR:2.15,95%置信区间[IC]:1.32至3.20,p=0.002)。
从孕期开始补充肌醇可降低妊娠期糖尿病的发病率,对于有明确危险因素的患者,每天4克的剂量作为预防策略可能具有价值。