肥胖和2型糖尿病患者的血管表观基因组:个性化治疗的机会

Vascular biology (Bristol, England) Pub Date : 2020-05-15 eCollection Date: 2020-01-01 DOI:10.1530/VB-20-0001
Sarah Costantino, Shafeeq A Mohammed, Samuele Ambrosini, Francesco Paneni
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引用次数: 4

摘要

我们的遗传背景提供了有限的个人风险发展血管并发症的信息。新的生物层,即表观遗传修饰,现在正在成为基因表达的有效调节因子,从而导致转录程序和血管疾病表型的改变。这种表观遗传修饰被定义为不涉及DNA序列变化的基因组变化,通常是由环境因素和不良的生活习惯引起的。值得注意的是,在生命中获得的不良表观遗传信号可以传递给后代,从而导致表观遗传和转录景观的过早改变,最终导致早期内皮功能障碍和血管衰老。表观基因组的修饰在心脏代谢紊乱(如肥胖和2型糖尿病)的病理生理中起着关键作用。在这些患者中,DNA甲基化和染色质结构的改变有助于改变调节胰岛素敏感性、葡萄糖稳态、脂肪生成和血管功能的途径。从这个角度来看,揭示心脏代谢患者的“表观遗传景观”可能有助于识别与肥胖和糖尿病相关血管功能障碍有关的新参与者,并可能为这种情况下的个性化治疗铺平道路。在这篇综述中,我们讨论了目前对代谢改变患者血管损伤和心血管疾病的表观遗传途径的了解。
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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The vascular epigenome in patients with obesity and type 2 diabetes: opportunities for personalized therapies.

Our genetic background provides limited information on individual risk of developing vascular complications overtime. New biological layers, namely epigenetic modifications, are now emerging as potent regulators of gene expression thus leading to altered transcriptional programs and vascular disease phenotypes. Such epigenetic modifications, defined as changes to the genome that do not involve changes in DNA sequence, are generally induced by environmental factors and poor lifestyle habits. Of note, adverse epigenetic signals acquired during life can be transmitted to the offspring thus leading to premature alterations of the epigenetic and transcriptional landscape eventually leading to early endothelial dysfunction and vascular senescence. Modifications of the epigenome play a pivotal role in the pathophysiology of cardiometabolic disturbances such as obesity and type 2 diabetes. In these patients, changes of DNA methylation and chromatin structure contribute to alter pathways regulating insulin sensitivity, glucose homeostasis, adipogenesis and vascular function. In this perspective, unveiling the 'epigenetic landscape' in cardiometabolic patients may help to identify new players implicated in obesity and diabetes-related vascular dysfunction and may pave the way for personalized therapies in this setting. In the present review, we discuss current knowledge of the epigenetic routes implicated in vascular damage and cardiovascular disease in patients with metabolic alterations.

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