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妊娠期糖尿病与发育编程。

Gestational Diabetes Mellitus and Developmental Programming.

机构信息

Singapore Institute for Clinical Sciences (SICS), Agency for Science, Technology and Research (A*STAR), Singapore, Singapore.

MRC Lifecourse Epidemiology Unit and NIHR Southampton Biomedical Research Centre, University of Southampton and University Hospital Southampton NHS Foundation Trust, Southampton, United Kingdom,

出版信息

Ann Nutr Metab. 2020;76 Suppl 3(Suppl 3):4-15. doi: 10.1159/000509902. Epub 2021 Jan 19.

Abstract

During normal pregnancy, increased insulin resistance acts as an adaptation to enhance materno-foetal nutrient transfer and meet the nutritional needs of the developing foetus, particularly in relation to glucose requirements. However, about 1 in 6 pregnancies worldwide is affected by the inability of the mother's metabolism to maintain normoglycaemia, with the combination of insulin resistance and insufficient insulin secretion resulting in gestational diabetes mellitus (GDM). A growing body of epidemiologic work demonstrates long-term implications for adverse offspring health resulting from exposure to GDM in utero. The effect of GDM on offspring obesity and cardiometabolic health may be partly influenced by maternal obesity; this suggests that improving glucose and weight control during early pregnancy, or better still before conception, has the potential to lessen the risk to the offspring. The consequences of GDM for microbiome modification in the offspring and the impact upon offspring immune dysregulation are actively developing research areas. Some studies have suggested that GDM impacts offspring neurodevelopmental and cognitive outcomes; confirmatory studies will need to separate the effect of GDM exposure from the complex interplay of social and environmental factors. Animal and human studies have demonstrated the role of epigenetic modifications in underpinning the predisposition to adverse health in offspring exposed to suboptimal hyperglycaemic in utero environment. To date, several epigenome-wide association studies in human have extended our knowledge on linking maternal diabetes-related DNA methylation marks with childhood adiposity-related outcomes. Identification of such epigenetic marks can help guide future research to develop candidate diagnostic biomarkers and preventive or therapeutic strategies. Longer-term interventions and longitudinal studies will be needed to better understand the causality, underlying mechanisms, or impact of GDM treatments to optimize the health of future generations.

摘要

在正常妊娠期间,胰岛素抵抗增加是一种适应机制,可增强母婴营养转移,并满足发育中胎儿的营养需求,尤其是与葡萄糖需求有关的营养需求。然而,全世界约有 1/6 的妊娠受到母亲代谢无法维持正常血糖水平的影响,胰岛素抵抗和胰岛素分泌不足导致妊娠糖尿病(GDM)。越来越多的流行病学研究表明,胎儿在子宫内暴露于 GDM 会对后代健康产生长期不良影响。GDM 对后代肥胖和心脏代谢健康的影响可能部分受到母亲肥胖的影响;这表明,改善妊娠早期或更好的是在受孕前的血糖和体重控制,有可能降低后代的风险。GDM 对后代微生物组修饰的影响及其对后代免疫失调的影响是正在积极发展的研究领域。一些研究表明,GDM 会影响后代的神经发育和认知结果;需要进行确认性研究,将 GDM 暴露的影响与社会和环境因素的复杂相互作用分开。动物和人类研究表明,表观遗传修饰在为后代提供易患不良健康的倾向方面发挥着重要作用,这些后代暴露于不理想的高血糖宫内环境中。迄今为止,人类的几项全基因组关联研究扩展了我们对将与母亲糖尿病相关的 DNA 甲基化标记与儿童肥胖相关结果联系起来的认识。鉴定这些表观遗传标记可以帮助指导未来的研究,以开发候选诊断生物标志物和预防或治疗策略。需要进行更长期的干预和纵向研究,以更好地了解 GDM 治疗的因果关系、潜在机制或影响,从而优化后代的健康。

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Gestational Diabetes Mellitus and Developmental Programming.妊娠期糖尿病与发育编程。
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