tetano
Editor, Senior Moderator
Am J Physiol Heart Circ Physiol
. 2020 Dec 4.
doi: 10.1152/ajpheart.00755.2020. Online ahead of print.
Sex Differences in COVID-19: Candidate Pathways, Genetics of ACE2, and Sex Hormones
Anissa Viveiros[SUP] 1 [/SUP], Jaslyn Rasmuson[SUP] 1 [/SUP], Jennie Vu[SUP] 1 [/SUP], Sharon L Mulvagh[SUP] 2 [/SUP], Cindy Y Y Yip[SUP] 3 [/SUP], Colleen M Norris[SUP] 4 [/SUP], Gavin Y Oudit[SUP] 5 [/SUP]
Affiliations
Abstract
Biological sex is increasingly recognized as a critical determinant of health and disease, particularly relevant to the topical COVID-19 pandemic caused by the SARS-CoV-2 coronavirus. Epidemiological data and observational reports from both the original SARS epidemic and the most recent COVID-19 pandemic have a common feature: males are more likely to exhibit enhanced disease severity and mortality than females. Sex differences in cardiovascular disease and COVID-19 share mechanistic foundations, namely the involvement of both the innate immune system and the canonical renin-angiotensin system (RAS). Immunological differences suggest that females mount a rapid and aggressive innate immune response, and the attenuated antiviral response in males may confer enhanced susceptibility to severe disease. Further, the ACE2 enzyme is involved in disease pathogenesis in cardiovascular disease and COVID-19, either to serve as a protective mechanism by deactivating the renin-angiotensin system or as the receptor for viral entry, respectively. Loss of membrane ACE2 and a corresponding increase in plasma ACE2 are associated with worsened cardiovascular disease outcomes, a mechanism attributed to A Disintegrin and Metalloproteinase (ADAM)17. SARS-CoV-2 infection also leads to ADAM17 activation, a positive feedback cycle that exacerbates ACE2 loss. Therefore, the relationship between cardiovascular disease and COVID-19 is critically dependent on the loss of membrane ACE2 by ADAM17-mediated proteolytic cleavage. This article will explore potential mechanisms involved in COVID-19 that may contribute to sex-specific susceptibility focusing on the innate immune system and the RAS, namely genetics and sex hormones. Finally, we will highlight the added challenges of gender in the COVID-19 pandemic.
Keywords: ACE2; COVID-19; SARS-CoV-2; cardiovascular disease; sex differences.
. 2020 Dec 4.
doi: 10.1152/ajpheart.00755.2020. Online ahead of print.
Sex Differences in COVID-19: Candidate Pathways, Genetics of ACE2, and Sex Hormones
Anissa Viveiros[SUP] 1 [/SUP], Jaslyn Rasmuson[SUP] 1 [/SUP], Jennie Vu[SUP] 1 [/SUP], Sharon L Mulvagh[SUP] 2 [/SUP], Cindy Y Y Yip[SUP] 3 [/SUP], Colleen M Norris[SUP] 4 [/SUP], Gavin Y Oudit[SUP] 5 [/SUP]
Affiliations
- PMID: 33275517
- DOI: 10.1152/ajpheart.00755.2020
Abstract
Biological sex is increasingly recognized as a critical determinant of health and disease, particularly relevant to the topical COVID-19 pandemic caused by the SARS-CoV-2 coronavirus. Epidemiological data and observational reports from both the original SARS epidemic and the most recent COVID-19 pandemic have a common feature: males are more likely to exhibit enhanced disease severity and mortality than females. Sex differences in cardiovascular disease and COVID-19 share mechanistic foundations, namely the involvement of both the innate immune system and the canonical renin-angiotensin system (RAS). Immunological differences suggest that females mount a rapid and aggressive innate immune response, and the attenuated antiviral response in males may confer enhanced susceptibility to severe disease. Further, the ACE2 enzyme is involved in disease pathogenesis in cardiovascular disease and COVID-19, either to serve as a protective mechanism by deactivating the renin-angiotensin system or as the receptor for viral entry, respectively. Loss of membrane ACE2 and a corresponding increase in plasma ACE2 are associated with worsened cardiovascular disease outcomes, a mechanism attributed to A Disintegrin and Metalloproteinase (ADAM)17. SARS-CoV-2 infection also leads to ADAM17 activation, a positive feedback cycle that exacerbates ACE2 loss. Therefore, the relationship between cardiovascular disease and COVID-19 is critically dependent on the loss of membrane ACE2 by ADAM17-mediated proteolytic cleavage. This article will explore potential mechanisms involved in COVID-19 that may contribute to sex-specific susceptibility focusing on the innate immune system and the RAS, namely genetics and sex hormones. Finally, we will highlight the added challenges of gender in the COVID-19 pandemic.
Keywords: ACE2; COVID-19; SARS-CoV-2; cardiovascular disease; sex differences.