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心血管系统衰老:从哈钦森-吉尔福德早衰综合征中得到的启示。

Aging in the Cardiovascular System: Lessons from Hutchinson-Gilford Progeria Syndrome.

机构信息

Centro Nacional de Investigaciones Cardiovasculares Carlos III (CNIC), 28029 Madrid, Spain; email:

CIBER de Enfermedades Cardiovasculares (CIBER-CV), 28029 Madrid, Spain.

出版信息

Annu Rev Physiol. 2018 Feb 10;80:27-48. doi: 10.1146/annurev-physiol-021317-121454. Epub 2017 Sep 20.

Abstract

Aging, the main risk factor for cardiovascular disease (CVD), is becoming progressively more prevalent in our societies. A better understanding of how aging promotes CVD is therefore urgently needed to develop new strategies to reduce disease burden. Atherosclerosis and heart failure contribute significantly to age-associated CVD-related morbimortality. CVD and aging are both accelerated in patients suffering from Hutchinson-Gilford progeria syndrome (HGPS), a rare genetic disorder caused by the prelamin A mutant progerin. Progerin causes extensive atherosclerosis and cardiac electrophysiological alterations that invariably lead to premature aging and death. This review summarizes the main structural and functional alterations to the cardiovascular system during physiological and premature aging and discusses the mechanisms underlying exaggerated CVD and aging induced by prelamin A and progerin. Because both proteins are expressed in normally aging non-HGPS individuals, and most hallmarks of normal aging occur in progeria, research on HGPS can identify mechanisms underlying physiological aging.

摘要

衰老是心血管疾病(CVD)的主要风险因素,在我们的社会中变得越来越普遍。因此,迫切需要更好地了解衰老如何促进 CVD,以制定新的策略来减轻疾病负担。动脉粥样硬化和心力衰竭是与年龄相关的 CVD 相关发病率和死亡率的主要原因。患有哈钦森-吉尔福德早衰综合征(HGPS)的患者中,CVD 和衰老都会加速,HGPS 是一种罕见的遗传疾病,由前层粘连蛋白 A 突变体早衰素引起。早衰素导致广泛的动脉粥样硬化和心脏电生理改变,不可避免地导致过早衰老和死亡。本综述总结了心血管系统在生理和早衰过程中的主要结构和功能改变,并讨论了前层粘连蛋白 A 和早衰素引起的 CVD 和衰老的放大机制。由于这两种蛋白都在正常衰老的非 HGPS 个体中表达,并且正常衰老的大多数特征都发生在早衰中,因此对 HGPS 的研究可以确定生理衰老的机制。

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