Your browser doesn't support javascript.
Higher mortality of COVID-19 in males: sex differences in immune response and cardiovascular comorbidities.
Bienvenu, Laura A; Noonan, Jonathan; Wang, Xiaowei; Peter, Karlheinz.
  • Bienvenu LA; Atherothrombosis and Vascular Biology Laboratory, Baker Heart and Diabetes Institute, 75 Commercial Rd, Melbourne, VIC 3004, Australia.
  • Noonan J; Molecular Imaging and Theranostics Laboratory, Baker Heart and Diabetes Institute, Melbourne, VIC, Australia.
  • Wang X; Department of Cardiometabolic Health, University of Melbourne, VIC, Australia.
  • Peter K; Atherothrombosis and Vascular Biology Laboratory, Baker Heart and Diabetes Institute, 75 Commercial Rd, Melbourne, VIC 3004, Australia.
Cardiovasc Res ; 116(14): 2197-2206, 2020 12 01.
Article in English | MEDLINE | ID: covidwho-872983
ABSTRACT
The high mortality rate of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) infection is a critical concern of the coronavirus disease 2019 (COVID-19) pandemic. Strikingly, men account for the majority of COVID-19 deaths, with current figures ranging from 59% to 75% of total mortality. However, despite clear implications in relation to COVID-19 mortality, most research has not considered sex as a critical factor in data analysis. Here, we highlight fundamental biological differences that exist between males and females, and how these may make significant contributions to the male-biased COVID-19 mortality. We present preclinical evidence identifying the influence of biological sex on the expression and regulation of angiotensin-converting enzyme 2 (ACE2), which is the main receptor used by SARS-CoV-2 to enter cells. However, we note that there is a lack of reports showing that sexual dimorphism of ACE2 expression exists and is of functional relevance in humans. In contrast, there is strong evidence, especially in the context of viral infections, that sexual dimorphism plays a central role in the genetic and hormonal regulation of immune responses, both of the innate and the adaptive immune system. We review evidence supporting that ineffective anti-SARS-CoV-2 responses, coupled with a predisposition for inappropriate hyperinflammatory responses, could provide a biological explanation for the male bias in COVID-19 mortality. A prominent finding in COVID-19 is the increased risk of death with pre-existing cardiovascular comorbidities, such as hypertension, obesity, and age. We contextualize how important features of sexual dimorphism and inflammation in COVID-19 may exhibit a reciprocal relationship with comorbidities, and explain their increased mortality risk. Ultimately, we demonstrate that biological sex is a fundamental variable of critical relevance to our mechanistic understanding of SARS-CoV-2 infection and the pursuit of effective COVID-19 preventative and therapeutic strategies.
Subject(s)
Keywords

Full text: Available Collection: International databases Database: MEDLINE Main subject: Cardiovascular Diseases / Health Status Disparities / SARS-CoV-2 / COVID-19 / Inflammation Type of study: Diagnostic study / Prognostic study Limits: Animals / Female / Humans / Male Language: English Journal: Cardiovasc Res Year: 2020 Document Type: Article Affiliation country: Cvr

Similar

MEDLINE

...
LILACS

LIS


Full text: Available Collection: International databases Database: MEDLINE Main subject: Cardiovascular Diseases / Health Status Disparities / SARS-CoV-2 / COVID-19 / Inflammation Type of study: Diagnostic study / Prognostic study Limits: Animals / Female / Humans / Male Language: English Journal: Cardiovasc Res Year: 2020 Document Type: Article Affiliation country: Cvr