Coronavirus Disease 2019 and Stroke: Clinical Manifestations and Pathophysiological Insights

J Stroke Cerebrovasc Dis. 2020 Aug;29(8):104941. doi: 10.1016/j.jstrokecerebrovasdis.2020.104941. Epub 2020 May 12.

Abstract

Coronavirus disease 2019 (COVID-19), caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), is a global health threat. Some COVID-19 patients have exhibited widespread neurological manifestations including stroke. Acute ischemic stroke, intracerebral hemorrhage, and cerebral venous sinus thrombosis have been reported in patients with COVID-19. COVID-19-associated coagulopathy is increasingly recognized as a result of acute infection and is likely caused by inflammation, including inflammatory cytokine storm. Recent studies suggest that axonal transport of SARS-CoV-2 to the brain can occur via the cribriform plate adjacent to the olfactory bulb that may lead to symptomatic anosmia. The internalization of SARS-CoV-2 is mediated by the binding of the spike glycoprotein of the virus to the angiotensin-converting enzyme 2 (ACE2) on cellular membranes. ACE2 is expressed in several tissues including lung alveolar cells, gastrointestinal tissue, and brain. The aim of this review is to provide insights into the clinical manifestations and pathophysiological mechanisms of stroke in COVID-19 patients. SARS-CoV-2 can down-regulate ACE2 and, in turn, overactivate the classical renin-angiotensin system (RAS) axis and decrease the activation of the alternative RAS pathway in the brain. The consequent imbalance in vasodilation, neuroinflammation, oxidative stress, and thrombotic response may contribute to the pathophysiology of stroke during SARS-CoV-2 infection.

Keywords: ACE2; COVID-19; Endothelial damage; Pandemic; Renin-angiotensin system; SARS-CoV-2; Stroke.

Publication types

  • Review

MeSH terms

  • Angiotensin-Converting Enzyme 2
  • Betacoronavirus / metabolism
  • Betacoronavirus / pathogenicity*
  • Blood Coagulation
  • Brain / metabolism
  • Brain / physiopathology*
  • Brain / virology
  • COVID-19
  • Coronavirus Infections / epidemiology
  • Coronavirus Infections / metabolism
  • Coronavirus Infections / physiopathology*
  • Coronavirus Infections / virology
  • Encephalitis, Viral / epidemiology
  • Encephalitis, Viral / metabolism
  • Encephalitis, Viral / physiopathology*
  • Encephalitis, Viral / virology
  • Host Microbial Interactions
  • Humans
  • Inflammation Mediators / metabolism
  • Oxidative Stress
  • Pandemics
  • Peptidyl-Dipeptidase A / metabolism
  • Pneumonia, Viral / epidemiology
  • Pneumonia, Viral / metabolism
  • Pneumonia, Viral / physiopathology*
  • Pneumonia, Viral / virology
  • Renin-Angiotensin System
  • SARS-CoV-2
  • Signal Transduction
  • Spike Glycoprotein, Coronavirus / metabolism
  • Stroke / epidemiology
  • Stroke / metabolism
  • Stroke / physiopathology*
  • Stroke / virology
  • Vasodilation
  • Virulence

Substances

  • Inflammation Mediators
  • Spike Glycoprotein, Coronavirus
  • spike protein, SARS-CoV-2
  • Peptidyl-Dipeptidase A
  • ACE2 protein, human
  • Angiotensin-Converting Enzyme 2