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SARS-CoV-2/COVID-19 in multiple sclerosis patients receiving disease-modifying therapy
At the end of 2019, the COVID-19 pandemic began, which at the time of writing continues to be a serious problem for many areas of medicine, including neurology. Since patients with multiple sclerosis (MS) often exhibit motor disability and receive disease-modifying therapy (DMT), which has an immuno...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7831713/ https://www.ncbi.nlm.nih.gov/pubmed/33388661 http://dx.doi.org/10.1016/j.clineuro.2020.106451 |
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author | Adamczyk-Sowa, Monika Mado, Hubert Kubicka-Bączyk, Katarzyna Jaroszewicz, Jerzy Sobala-Szczygieł, Barbara Bartman, Wojciech Sowa, Paweł |
author_facet | Adamczyk-Sowa, Monika Mado, Hubert Kubicka-Bączyk, Katarzyna Jaroszewicz, Jerzy Sobala-Szczygieł, Barbara Bartman, Wojciech Sowa, Paweł |
author_sort | Adamczyk-Sowa, Monika |
collection | PubMed |
description | At the end of 2019, the COVID-19 pandemic began, which at the time of writing continues to be a serious problem for many areas of medicine, including neurology. Since patients with multiple sclerosis (MS) often exhibit motor disability and receive disease-modifying therapy (DMT), which has an immunosuppressive effect, it is plausible that this will affect the susceptibility of MS patients to COVID-19, as well as the course of this disease. However, current data indicate that the use of DMT does not cause negative prognosis in COVID-19 sufferers, but the motor disability progression associated with MS does. In this study, we present the case reports of 4 patients with relapsing-remitting MS, who developed COVID-19, and despite the use of DMT the course of the disease was mild. Two patients were treated with dimethyl fumarate, one with Interferon β1b and one with glatiramer acetate. One of the patients using dimethyl fumarate had lymphopenia. All patients had symptoms of COVID-19 from the nervous system, the most frequent being headache, which occurred in all patients. The aim of this article is to present a case series of four patients with MS and COVID-19, and to discuss the available literature on COVID-19 in patients with MS, with particular consideration of the impact of DMT. |
format | Online Article Text |
id | pubmed-7831713 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-78317132021-01-26 SARS-CoV-2/COVID-19 in multiple sclerosis patients receiving disease-modifying therapy Adamczyk-Sowa, Monika Mado, Hubert Kubicka-Bączyk, Katarzyna Jaroszewicz, Jerzy Sobala-Szczygieł, Barbara Bartman, Wojciech Sowa, Paweł Clin Neurol Neurosurg Article At the end of 2019, the COVID-19 pandemic began, which at the time of writing continues to be a serious problem for many areas of medicine, including neurology. Since patients with multiple sclerosis (MS) often exhibit motor disability and receive disease-modifying therapy (DMT), which has an immunosuppressive effect, it is plausible that this will affect the susceptibility of MS patients to COVID-19, as well as the course of this disease. However, current data indicate that the use of DMT does not cause negative prognosis in COVID-19 sufferers, but the motor disability progression associated with MS does. In this study, we present the case reports of 4 patients with relapsing-remitting MS, who developed COVID-19, and despite the use of DMT the course of the disease was mild. Two patients were treated with dimethyl fumarate, one with Interferon β1b and one with glatiramer acetate. One of the patients using dimethyl fumarate had lymphopenia. All patients had symptoms of COVID-19 from the nervous system, the most frequent being headache, which occurred in all patients. The aim of this article is to present a case series of four patients with MS and COVID-19, and to discuss the available literature on COVID-19 in patients with MS, with particular consideration of the impact of DMT. Elsevier B.V. 2021-02 2020-12-29 /pmc/articles/PMC7831713/ /pubmed/33388661 http://dx.doi.org/10.1016/j.clineuro.2020.106451 Text en © 2020 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Adamczyk-Sowa, Monika Mado, Hubert Kubicka-Bączyk, Katarzyna Jaroszewicz, Jerzy Sobala-Szczygieł, Barbara Bartman, Wojciech Sowa, Paweł SARS-CoV-2/COVID-19 in multiple sclerosis patients receiving disease-modifying therapy |
title | SARS-CoV-2/COVID-19 in multiple sclerosis patients receiving disease-modifying therapy |
title_full | SARS-CoV-2/COVID-19 in multiple sclerosis patients receiving disease-modifying therapy |
title_fullStr | SARS-CoV-2/COVID-19 in multiple sclerosis patients receiving disease-modifying therapy |
title_full_unstemmed | SARS-CoV-2/COVID-19 in multiple sclerosis patients receiving disease-modifying therapy |
title_short | SARS-CoV-2/COVID-19 in multiple sclerosis patients receiving disease-modifying therapy |
title_sort | sars-cov-2/covid-19 in multiple sclerosis patients receiving disease-modifying therapy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7831713/ https://www.ncbi.nlm.nih.gov/pubmed/33388661 http://dx.doi.org/10.1016/j.clineuro.2020.106451 |
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