Aging- and gender-related modulation of RAAS: potential implications in COVID-19 disease.

Vascular biology (Bristol, England) Pub Date : 2020-12-11 eCollection Date: 2021-01-01 DOI:10.1530/VB-20-0014
Laura Monteonofrio, Maria Cristina Florio, Majd AlGhatrif, Edward G Lakatta, Maurizio C Capogrossi
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引用次数: 11

Abstract

Coronavirus disease 2019 (COVID-19) is a new infectious disease caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). COVID-19 is frequently characterized by a marked inflammatory response with severe pneumonia and respiratory failure associated with multiorgan involvement. Some risk factors predispose patients to develop a more severe infection and to an increased mortality; among them, advanced age and male gender have been identified as major and independent risk factors for COVID-19 poor outcome. The renin-angiotensin-aldosterone system (RAAS) is strictly involved in COVID-19 because angiotensin converting enzyme 2 (ACE2) is the host receptor for SARS-CoV-2 and also converts pro-inflammatory angiotensin (Ang) II into anti-inflammatory Ang(1-7). In this review, we have addressed the effect of aging and gender on RAAS with emphasis on ACE2, pro-inflammatory Ang II/Ang II receptor 1 axis and anti-inflammatory Ang(1-7)/Mas receptor axis.

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与年龄和性别相关的RAAS调节:对COVID-19疾病的潜在影响
冠状病毒病2019 (COVID-19)是由严重急性呼吸综合征冠状病毒2 (SARS-CoV-2)引起的一种新型传染病。COVID-19通常以明显的炎症反应为特征,伴有严重肺炎和与多器官受累相关的呼吸衰竭。一些危险因素易使患者发生更严重的感染并增加死亡率;其中,高龄和男性性别已被确定为COVID-19预后不良的主要独立危险因素。肾素-血管紧张素-醛固酮系统(RAAS)与COVID-19密切相关,因为血管紧张素转换酶2 (ACE2)是SARS-CoV-2的宿主受体,并将促炎血管紧张素(Ang) II转化为抗炎Ang(1-7)。在这篇综述中,我们讨论了年龄和性别对RAAS的影响,重点是ACE2、促炎Ang II/Ang II受体1轴和抗炎Ang(1-7)/Mas受体轴。
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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