Center for Molecular Cardiology, University of Zürich, Schlieren, Switzerland.
Department of Internal Medicine, First Clinic of Internal Medicine, University of Genoa, Genoa, Italy.
Basic Clin Pharmacol Toxicol. 2020 Aug;127(2):120-131. doi: 10.1111/bcpt.13426. Epub 2020 Jul 16.
Over the last century, Western societies experienced a demographic shift driven by increased lifespan and decreased fertility, resulting in the subversion of the world's demographic pyramid. In ageing societies, cardiovascular diseases are the major cause of morbidity and mortality, thus representing a major societal and economic burden. Indeed, ageing associates with the deterioration of a genetic network implicated in senescence and longevity, orchestrating deleterious cellular processes that converge in the structural and functional decline of both the myocardium and the vasculature. In this review, we revise a compendium of genes involved in these processes and delineate possible strategies to interfere with them. Dietary interventions (eg intermittent fasting) and sirtuin-activating compounds are among the most promising interventions shown to promote protective effects on the ageing cardiovascular system. We conclude that ageing and longevity genes modulate cardiovascular function by acting on deleterious downstream processes such as inflammation and oxidative stress, thus representing promising targets for the prevention and treatment of age-related cardiovascular dysfunction.
在上个世纪,西方社会经历了由寿命延长和生育率下降驱动的人口结构转变,导致世界人口金字塔发生了颠覆。在老龄化社会中,心血管疾病是发病率和死亡率的主要原因,因此给社会和经济带来了重大负担。事实上,衰老与参与衰老和长寿的遗传网络的恶化有关,协调有害的细胞过程,这些过程集中在心肌和脉管系统的结构和功能下降上。在这篇综述中,我们回顾了涉及这些过程的基因,并描述了可能的干预策略。饮食干预(例如间歇性禁食)和 sirtuin 激活化合物是最有前途的干预措施之一,它们显示出对衰老心血管系统的保护作用。我们得出结论,衰老和长寿基因通过作用于炎症和氧化应激等有害下游过程来调节心血管功能,因此代表了预防和治疗与年龄相关的心血管功能障碍的有前途的靶点。