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De Novo Movement Disorders and COVID‐19: Exploring the Interface
BACKGROUND: Neurological manifestations of severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) are being widely documented. However, movement disorders in the setting of 2019 coronavirus infectious disease (COVID‐19) have been a strikingly less discussed topic. OBJECTIVES: To summarize avai...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8250792/ https://www.ncbi.nlm.nih.gov/pubmed/34230886 http://dx.doi.org/10.1002/mdc3.13224 |
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author | Ghosh, Ritwik Biswas, Uttam Roy, Dipayan Pandit, Alak Lahiri, Durjoy Ray, Biman Kanti Benito‐León, Julián |
author_facet | Ghosh, Ritwik Biswas, Uttam Roy, Dipayan Pandit, Alak Lahiri, Durjoy Ray, Biman Kanti Benito‐León, Julián |
author_sort | Ghosh, Ritwik |
collection | PubMed |
description | BACKGROUND: Neurological manifestations of severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) are being widely documented. However, movement disorders in the setting of 2019 coronavirus infectious disease (COVID‐19) have been a strikingly less discussed topic. OBJECTIVES: To summarize available pieces of evidence documenting de novo movement disorders in COVID‐19. METHODS: We used the existing PRISMA consensus statement. Data were collected from PubMed, EMBASE, Web of Science, and Scopus databases up to the 29th January, 2021, using pre‐specified searching strategies. RESULTS: Twenty‐two articles were selected for the qualitative synthesis. Among these, a total of 52 patients with de novo movement disorders were reported. Most of these had myoclonus, ataxia, tremor or a combination of these, while three had parkinsonism and one a functional disorder. In general, they were managed successfully by intravenous immunoglobulin or steroids. Some cases, primarily with myoclonus, could be ascribed to medication exposures, metabolic disturbances or severe hypoxia, meanwhile others to a post‐or para‐infectious immune‐mediated mechanism. SARS‐CoV‐2 could also invade the central nervous system, through vascular or retrograde axonal pathways, and cause movement disorders by two primary mechanisms. Firstly, through the downregulation of angiotensin‐converting enzyme 2 receptors, resulting in the imbalance of dopamine and norepinephrine; and secondly, the virus could cause cellular vacuolation, demyelination and gliosis, leading to encephalitis and associated movement disorders. CONCLUSION: De novo movement disorders are scantly reported in COVID‐19. The links between SARS‐CoV‐2 and movement disorders are not yet established. However, we should closely monitor COVID‐19 survivors for the possibility of post‐COVID movement disorders. |
format | Online Article Text |
id | pubmed-8250792 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-82507922021-07-02 De Novo Movement Disorders and COVID‐19: Exploring the Interface Ghosh, Ritwik Biswas, Uttam Roy, Dipayan Pandit, Alak Lahiri, Durjoy Ray, Biman Kanti Benito‐León, Julián Mov Disord Clin Pract Reviews BACKGROUND: Neurological manifestations of severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) are being widely documented. However, movement disorders in the setting of 2019 coronavirus infectious disease (COVID‐19) have been a strikingly less discussed topic. OBJECTIVES: To summarize available pieces of evidence documenting de novo movement disorders in COVID‐19. METHODS: We used the existing PRISMA consensus statement. Data were collected from PubMed, EMBASE, Web of Science, and Scopus databases up to the 29th January, 2021, using pre‐specified searching strategies. RESULTS: Twenty‐two articles were selected for the qualitative synthesis. Among these, a total of 52 patients with de novo movement disorders were reported. Most of these had myoclonus, ataxia, tremor or a combination of these, while three had parkinsonism and one a functional disorder. In general, they were managed successfully by intravenous immunoglobulin or steroids. Some cases, primarily with myoclonus, could be ascribed to medication exposures, metabolic disturbances or severe hypoxia, meanwhile others to a post‐or para‐infectious immune‐mediated mechanism. SARS‐CoV‐2 could also invade the central nervous system, through vascular or retrograde axonal pathways, and cause movement disorders by two primary mechanisms. Firstly, through the downregulation of angiotensin‐converting enzyme 2 receptors, resulting in the imbalance of dopamine and norepinephrine; and secondly, the virus could cause cellular vacuolation, demyelination and gliosis, leading to encephalitis and associated movement disorders. CONCLUSION: De novo movement disorders are scantly reported in COVID‐19. The links between SARS‐CoV‐2 and movement disorders are not yet established. However, we should closely monitor COVID‐19 survivors for the possibility of post‐COVID movement disorders. John Wiley & Sons, Inc. 2021-04-28 /pmc/articles/PMC8250792/ /pubmed/34230886 http://dx.doi.org/10.1002/mdc3.13224 Text en © 2021 International Parkinson and Movement Disorder Society |
spellingShingle | Reviews Ghosh, Ritwik Biswas, Uttam Roy, Dipayan Pandit, Alak Lahiri, Durjoy Ray, Biman Kanti Benito‐León, Julián De Novo Movement Disorders and COVID‐19: Exploring the Interface |
title | De Novo Movement Disorders and COVID‐19: Exploring the Interface |
title_full | De Novo Movement Disorders and COVID‐19: Exploring the Interface |
title_fullStr | De Novo Movement Disorders and COVID‐19: Exploring the Interface |
title_full_unstemmed | De Novo Movement Disorders and COVID‐19: Exploring the Interface |
title_short | De Novo Movement Disorders and COVID‐19: Exploring the Interface |
title_sort | de novo movement disorders and covid‐19: exploring the interface |
topic | Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8250792/ https://www.ncbi.nlm.nih.gov/pubmed/34230886 http://dx.doi.org/10.1002/mdc3.13224 |
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