Stopping the Intergenerational Risk of Diabetes-From Mechanisms to Interventions: A Report on Research Supported by Pathway to Stop Diabetes.

Diabetes Pub Date : 2025-03-01 DOI:10.2337/dbi24-0014
Soren Harnois-Leblanc, Marie-France Hivert
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Abstract

Embedded in the developmental origins of health and disease (DOHaD) hypothesis, maternal hyperglycemia in utero, from preexisting diabetes or gestational diabetes mellitus, predisposes the offspring to excess adiposity and heightened risk of prediabetes and type 2 diabetes development. This transmission creates a vicious cycle increasing the presence of diabetes from one generation to another, leading to the question: How can we interrupt this vicious cycle? In this article, we present the current state of knowledge on the intergenerational transmission of diabetes from epidemiological life course studies. Then, we discuss the potential mechanisms implicated in the intergenerational transmission of diabetes with a focus on epigenetics. We present novel findings stemming from epigenome-wide association studies of offspring DNA methylation in blood and placental tissues, which shed light on potential molecular mechanisms implicated in the mother-offspring transmission of diabetes. Lastly, with a perspective on how to break the cycle, we consider interventions to prevent offspring obesity and diabetes development before puberty, as a critical period of the intergenerational cycle. This article is part of a series of perspectives that report on research funded by the American Diabetes Association Pathway to Stop Diabetes program.

阻止糖尿病的代际风险--从机制到干预措施。
根据 "健康与疾病的发育起源 "假说,母体在子宫内的高血糖,包括原有的糖尿病或妊娠糖尿病,会导致后代脂肪过多,增加患糖尿病前期和 2 型糖尿病的风险。这种遗传造成了一种恶性循环,使糖尿病的发病率一代比一代高,这就引出了一个问题:我们如何才能阻断这种恶性循环?在这篇 "视角 "文章中,我们介绍了流行病学生命历程研究中有关糖尿病代际传播的知识现状。然后,我们讨论了糖尿病代际传播的潜在机制,重点是表观遗传学。我们介绍了对后代血液和胎盘组织中 DNA 甲基化的全表观遗传学关联研究的新发现,这些发现揭示了糖尿病母婴传播的潜在分子机制。最后,我们从如何打破这一循环的角度出发,考虑了在青春期之前预防后代肥胖和糖尿病发展的干预措施,因为青春期是代际循环的关键时期。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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