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There is evidence that the SARS-CoV-2 coronavirus causing the 2019 disease (COVID-19) has neurologic manifestations, and data and knowledge are accumulating at a fast pace. This has been documented with other coronaviruses as well; but, at the moment, it remains unclear to what extent SARS-CoV-2 exhibits neurotropism and whether the neurological manifestations are due to direct CNS effects or to secondary mechanisms. This review summarizes the available information on coronavirus effects on the nervous system, with an emphasis on the etiopathogenesis of SARS-CoV-2 CNS effects. Other neurotropic coronaviruses include HCoV-OC43, SARS-CoV-1, MERS-CoV, and the mouse hepatitis virus. The main neurologic manifestations of COVID-19 are headache, anosmia and ageusia, impaired consciousness, seizures, stroke and vascular events, and Guillain-Barré syndrome and peripheral nerve disorders. The possible CNS effects of treatments used for COVID-19 are also discussed, as are special considerations for patients with chronic neurological conditions.
This is a timely and useful read for practitioners of neurology in all settings.
– Codrin I. Lungu, MD
This abstract is available on the publisher's site.
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) emerged in December 2019, causing human coronavirus disease 2019 (COVID-19), which has now spread into a worldwide pandemic. The pulmonary manifestations of COVID-19 have been well described in the literature. Two similar human coronaviruses that cause Middle East respiratory syndrome (MERS-CoV) and severe acute respiratory syndrome (SARS-CoV-1) are known to cause disease in the central and peripheral nervous systems. Emerging evidence suggests COVID-19 has neurologic consequences as well.
This review serves to summarize available information regarding coronaviruses in the nervous system, identify the potential tissue targets and routes of entry of SARS-CoV-2 into the central nervous system, and describe the range of clinical neurological complications that have been reported thus far in COVID-19 and their potential pathogenesis. Viral neuroinvasion may be achieved by several routes, including transsynaptic transfer across infected neurons, entry via the olfactory nerve, infection of vascular endothelium, or leukocyte migration across the blood-brain barrier. The most common neurologic complaints in COVID-19 are anosmia, ageusia, and headache, but other diseases, such as stroke, impairment of consciousness, seizure, and encephalopathy, have also been reported.
Conclusions and Relevance
Recognition and understanding of the range of neurological disorders associated with COVID-19 may lead to improved clinical outcomes and better treatment algorithms. Further neuropathological studies will be crucial to understanding the pathogenesis of the disease in the central nervous system, and longitudinal neurologic and cognitive assessment of individuals after recovery from COVID-19 will be crucial to understand the natural history of COVID-19 in the central nervous system and monitor for any long-term neurologic sequelae.