Department of Medicine, Université de Sherbrooke, 3001, 12e ave Nord, Sherbrooke, QC, Canada.
Curr Diab Rep. 2013 Apr;13(2):238-44. doi: 10.1007/s11892-012-0360-x.
Insulin resistance is a component of the pathophysiology of both type 2 diabetes and gestational diabetes mellitus (GDM), but is also characteristic of normal glycemic physiology during pregnancy. In recent years, many studies have tried to understand determinants of insulin resistance in normal pregnancy and GDM, revealing that the placenta is capable of secreting many cytokines and hormones, classically considered as adipokines. More specifically, it appears that leptin and TNFα could be implicated in gestational insulin resistance and GDM pathophysiology. In addition, the maternal metabolic milieu was also identified as a key determinant of later insulin resistance in offspring, a phenomenon often described as 'fetal programming'. This article reviews the established risk factors and the more novel suspected biomarkers involved in maternal insulin resistance during pregnancy as well as the maternal and early life determinants of insulin resistance in offspring later in their life. We are also highlighting recent reports of the potential mechanisms involved in 'programming' of insulin resistance such as epigenetic modulation.
胰岛素抵抗是 2 型糖尿病和妊娠期糖尿病(GDM)病理生理学的一个组成部分,但也是妊娠期间正常血糖生理学的特征。近年来,许多研究试图了解正常妊娠和 GDM 中胰岛素抵抗的决定因素,结果表明胎盘能够分泌许多细胞因子和激素,这些激素通常被认为是脂肪因子。更具体地说,瘦素和 TNFα 似乎与妊娠期胰岛素抵抗和 GDM 病理生理学有关。此外,母体代谢环境也被确定为后代以后胰岛素抵抗的关键决定因素,这种现象通常被描述为“胎儿编程”。本文综述了妊娠期间母体胰岛素抵抗的既定危险因素和更新型的可疑生物标志物,以及后代以后生活中母体和早期生活决定因素与胰岛素抵抗的关系。我们还强调了最近关于胰岛素抵抗“编程”相关潜在机制的报告,如表观遗传调节。