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Biomedical Perspectives of Acute and Chronic Neurological and Neu-ropsychiatric Sequelae of COVID-19

  • George B. Stefano
  • , Pascal Büttiker
  • , Simon Weissenberger
  • , Radek Ptacek
  • , Fuzhou Wang
  • , Tobias Esch
  • , Thomas V. Bilfinger
  • , Jiri Raboch
  • , Richard M. Kream

Research output: Contribution to journalArticlepeer-review

26 Scopus citations

Abstract

The incidence of infections from severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the etiologic agent for coronavirus disease 2019 (COVID-19), has dramatically es-calated following the initial outbreak in China, in late 2019, resulting in a global pandemic with millions of deaths. Although the majority of infected patients survive, and the rapid advent and de-ployment of vaccines have afforded increased immunity against SARS-CoV-2, long-term sequelae of SARS-CoV-2 infection have become increasingly recognized. These include, but are not limited to, chronic pulmonary disease, cardiovascular disorders, and proinflammatory-associated neurological dysfunction that may lead to psychological and neurocognitive impairment. A major compo-nent of cognitive dysfunction is operationally categorized as “brain fog” which comprises difficul-ty concentrating, forgetfulness, confusion, depression, and fatigue. Multiple parameters associated with long-term neuropsychiatric sequelae of SARS-CoV-2 infection have been detailed in clinical studies. Empirically elucidated mechanisms associated with the neuropsychiatric manifestations of COVID-19 are by nature complex, but broad-based working models have focused on mitochon-drial dysregulation, leading to systemic reductions of metabolic activity and cellular bioenergetics within the CNS structures. Multiple factors underlying the expression of brain fog may facilitate future pathogenic insults, leading to repetitive cycles of viral and bacterial propagation. Interestingly, diverse neurocognitive sequelae associated with COVID-19 are not dissimilar from those observed in other historical pandemics, thereby providing a broad and integrative perspective on potential common mechanisms of CNS dysfunction subsequent to viral infection. Poor mental health status may be reciprocally linked to compromised immune processes and enhanced susceptibility to infection by diverse pathogens. By extrapolation, we contend that COVID-19 may potentiate the severity of neurological/neurocognitive deficits in patients afflicted by well-studied neurodegenerative di-sorders, such as Alzheimer's disease and Parkinson’s disease. Accordingly, the prevention, diagno-sis, and management of sustained neuropsychiatric manifestations of COVID-19 are pivotal health care directives and provide a compelling rationale for careful monitoring of infected patients, as early mitigation efforts may reduce short-and long-term complications.

Original languageEnglish
Pages (from-to)1229-1240
Number of pages12
JournalCurrent Neuropharmacology
Volume20
Issue number6
DOIs
StatePublished - Jun 2022

Keywords

  • COVID-19
  • Central nervous system
  • SARS-CoV-2
  • anxiety
  • brain fog
  • cognitive impairment
  • depression
  • long COVID
  • microglia
  • mitochondria
  • neuroinflammation
  • neuropsychiatric disease

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