Role of ACE2 polymorphism in COVID-19: impact of age
- PMID: 33984877
- DOI: 10.1515/cclm-2020-1877
Role of ACE2 polymorphism in COVID-19: impact of age
Abstract
More than 2 million people have died as a result of the COVID-19 outbreak. Angiotensin-converting enzyme 2 (ACE2) is a counter-regulatory enzyme that converts angiotensin-2 to Ang-(1-7) form in the renin-angiotensin system. Several studies have been analyzed the correlation between ACE2 and COVID-19. Indeed, ACE2/Ang (1-7) system protects the lung against acute respiratory distress syndrome by its anti-inflammatory/anti-oxidant function. However, SARS-Cov-2 can use ACE2 for host cell entry. Expression of ACE2 can be altered by several factors, including hypertension, diabetes and obesity, which also could increase the severity of COVID-19 infection. Besides, since androgens increase the expression of ACE-2, males are at higher risks of COVID-19 infection. Although reported statistics showed a significantly different infection risks of COVID-19 between adults and children, the reason behind the different responses is still unclear. This review proposes the effect of ACE polymorphism on the severity of SARS-COV-2 induced pneumonia. The previous meta-analysis regarding the effect of ACE polymorphism on the severity of pneumonia showed that polymorphism only affects the adult's illness severity and not the children. Two recent meta-analyses examined the effect of ACE polymorphism on the prevalence and mortality rate of COVID-19 and reported contradicting results. Our opinion paper suggests that the effect of ACE polymorphism on the severity of COVID-19 depends on the patients age, same as of the pneumonia.
Keywords: COVID-19; angiotensin-converting enzyme; plasma proteins; polymorphism.
© 2021 Walter de Gruyter GmbH, Berlin/Boston.
Comment in
-
Ageing, ACE2 deficiency and bad outcome in COVID-19.Clin Chem Lab Med. 2021 Jun 14;59(10):1607-1609. doi: 10.1515/cclm-2021-0658. Clin Chem Lab Med. 2021. PMID: 34118797 No abstract available.
References
-
- Young, MJ, Clyne, CD, Chapman, KE. Endocrine aspects of ACE2 regulation: RAAS, steroid hormones and SARS-CoV-2. J Endocrinol 2020;247:R45–62. https://doi.org/10.1530/joe-20-0260.
-
- Lanza, K, Perez, LG, Costa, LB, Cordeiro, TM, Palmeira, VA, Ribeiro, VT, et al.. COVID-19: the renin-angiotensin system imbalance hypothesis. Clin Sci (Lond) 2020;134:1259–64. https://doi.org/10.1042/cs20200492.
-
- Pal, R, Bhansali, A. COVID-19, diabetes mellitus and ACE2: the conundrum. Diabetes Res Clin Pract 2020;162:108132. https://doi.org/10.1016/j.diabres.2020.108132.
-
- Hoffmann, M, Kleine-Weber, H, Schroeder, S, Krüger, N, Herrler, T, Erichsen, S, et al.. SARS-CoV-2 cell entry depends on ACE2 and TMPRSS2 and is blocked by a clinically proven protease inhibitor. Cell 2020;181:271–80. https://doi.org/10.1016/j.cell.2020.02.052.
-
- Lu, R, Zhao, X, Li, J, Niu, P, Yang, B, Wu, H, et al.. Genomic characterisation and epidemiology of 2019 novel coronavirus: implications for virus origins and receptor binding. Lancet 2020;395:565–74. https://doi.org/10.1016/s0140-6736(20)30251-8.
LinkOut - more resources
Full Text Sources
Other Literature Sources
Miscellaneous