COVID-19 in multiple sclerosis patients and risk factors for severe infection
- PMID: 32980780
- PMCID: PMC7834402
- DOI: 10.1016/j.jns.2020.117147
COVID-19 in multiple sclerosis patients and risk factors for severe infection
Abstract
Multiple sclerosis (MS) patients have been considered a higher-risk population for COVID-19 due to the high prevalence of disability and disease-modifying therapy use; however, there is little data identifying clinical characteristics of MS associated with worse COVID-19 outcomes. Therefore, we conducted a multicenter prospective cohort study looking at the outcomes of 40 MS patients with confirmed COVID-19. Severity of COVID-19 infection was based on hospital course, where a mild course was defined as the patient not requiring hospital admission, moderate severity was defined as the patient requiring hospital admission to the general floor, and most severe was defined as requiring intensive care unit admission and/or death. 19/40(47.5%) had mild courses, 15/40(37.5%) had moderate courses, and 6/40(15%) had severe courses. Patients with moderate and severe courses were significantly older than those with a mild course (57[50-63] years old and 66[58.8-69.5] years old vs 48[40-51.5] years old, P = 0.0121, P = 0.0373). There was differing prevalence of progressive MS phenotype in those with more severe courses (severe:2/6[33.3%]primary-progressing and 0/6[0%]secondary-progressing, moderate:1/14[7.14%] and 5/14[35.7%] vs mild:0/19[0%] and 1/19[5.26%], P = 0.0075, 1 unknown). Significant disability was found in 1/19(5.26%) mild course-patients, but was in 9/15(60%, P = 0.00435) of moderate course-patients and 2/6(33.3%, P = 0.200) of severe course-patients. Disease-modifying therapy prevalence did not differ among courses (mild:17/19[89.5%], moderate:12/15[80%] and severe:3/6[50%], P = 0.123). MS patients with more severe COVID-19 courses tended to be older, were more likely to suffer from progressive phenotype, and had a higher degree of disability. However, disease-modifying therapy use was not different among courses.
Keywords: COVID-19; Coronavirus; Disease-modifying therapy; Multiple sclerosis; SARS-CoV-2019.
Copyright © 2020 Elsevier B.V. All rights reserved.
Conflict of interest statement
Dr. Adil Javed, MD, PhD has received consultation fee or honoraria from Serono, Sanofi-Genzyme, Novartis, Biogen, Celgene and Genentech. Dr. Mirela Cerghet MD, PhD has received grants for participation in clinical trials from Merck/EMD Serono, Roche, Novartis, Biogen, and Actelion. Dr. Eva Bernitsas MD has received grants from Novartis, Roche/Genetech, Medimmune, Chugai, ADAMAS, TG TG Therapeutics, Sanofi/Genzyme, and Mallinckrodt. She is also a consultant for Biogen, BMS, EMD Serono, and Roche/Genetech. Dr. Robert Lisak MD has received grants for participation in clinical trials from Ra Pharmaceuticals, Alexion, Argenx, Catalyst, Novartis, Medimmune, Genetech, Teva Pharmaceuticals and Mallinckdrot. He is also a consultant for Mallinckdrot, Novartis, Argenx, GLG Consulting, Alpha Sites Consulting, Schlesinger Group Consulting, Alpha Sites Consulting, Guidepoint Consulting, Informa Consulting, Haven Consulting, Cello Health Bioconsulting, and kc2 Medical Communications.
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