The Intersection between COVID-19, the Gene Family of ACE2 and Alzheimer’s Disease

Author:

Haghighi Mahdi Montazer1,Kakhki Erfan Ghani12,Sato Christine1,Ghani Mahdi2,Rogaeva Ekaterina13ORCID

Affiliation:

1. Tanz Centre for Research in Neurodegenerative Diseases, University of Toronto, Toronto, ON, Canada

2. DisorDATA Analytics, Ottawa, ON, Canada

3. Division of Neurology, Department of Medicine, University of Toronto, Toronto, Canada

Abstract

We reviewed factors that might influence COVID-19 outcomes (eg, neurological symptoms), including the link to Alzheimer’s disease. Since the virus triggers COVID-19 infection through binding to ACE2, we focused on the ACE2 gene family, including ACE. Both ACE2 and ACE are involved in the renin–angiotensin system (RAS). In general, ACE causes inflammation and vasoconstriction, while ACE2 leads to anti-inflammation activity and vasodilation. The disturbed balance between these counter-regulatory pathways could influence susceptibility to COVID-19. Notably, dysregulation of the RAS-equilibrium contributes to Alzheimer’s disease. Differences in the incidence and symptoms of COVID-19 in diverse populations could be attributed to variability in the human genome. For example, ACE and ACE2 variations could modify the outcome of COVID-19 in different populations. It would be important to conduct genome-wide studies to detect variants influencing COVID-19 presentation, with a special focus on variants affecting immune-related pathways and expression of RAS-related genes.

Publisher

SAGE Publications

Subject

General Neuroscience

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