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dc.contributor.authorSimpson-Yap, Sen_US
dc.contributor.authorPirmani, Aen_US
dc.contributor.authorKalincik, Ten_US
dc.contributor.authorDe Brouwer, Een_US
dc.contributor.authorGeys, Len_US
dc.contributor.authorParciak, Ten_US
dc.contributor.authorHelme, Aen_US
dc.contributor.authorRijke, Nen_US
dc.contributor.authorHillert, JAen_US
dc.contributor.authorMoreau, Yen_US
dc.contributor.authorEdan, Gen_US
dc.contributor.authorSharmin, Sen_US
dc.contributor.authorSpelman, Ten_US
dc.contributor.authorMcBurney, Ren_US
dc.contributor.authorSchmidt, Hen_US
dc.contributor.authorBergmann, ABen_US
dc.contributor.authorBraune, Sen_US
dc.contributor.authorStahmann, Aen_US
dc.contributor.authorMiddleton, RMen_US
dc.contributor.authorSalter, Aen_US
dc.contributor.authorBebo, Ben_US
dc.contributor.authorVan der Walt, Aen_US
dc.contributor.authorButzkueven, Hen_US
dc.contributor.authorOzakbas, Sen_US
dc.contributor.authorBoz, Cen_US
dc.contributor.authorKarabudak, Ren_US
dc.contributor.authorAlroughani, Ren_US
dc.contributor.authorRojas, JIen_US
dc.contributor.authorvan der Mei, IAen_US
dc.contributor.authorSciascia do Olival, Gen_US
dc.contributor.authorMagyari, Men_US
dc.contributor.authorAlonso, RNen_US
dc.contributor.authorNicholas, RSen_US
dc.contributor.authorChertcoff, ASen_US
dc.contributor.authorde Torres, AZen_US
dc.contributor.authorArrambide, Gen_US
dc.contributor.authorNag, Nen_US
dc.contributor.authorDescamps, Aen_US
dc.contributor.authorCosters, Len_US
dc.contributor.authorDobson, Ren_US
dc.contributor.authorMiller, Aen_US
dc.contributor.authorRodrigues, Pen_US
dc.contributor.authorPrčkovska, Ven_US
dc.contributor.authorComi, Gen_US
dc.contributor.authorPeeters, LMen_US
dc.date.accessioned2022-09-15T10:39:13Z
dc.date.available2022-07-27en_US
dc.date.issued2022-11en_US
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/80533
dc.description.abstractBACKGROUND AND OBJECTIVES: Certain demographic and clinical characteristics, including the use of some disease-modifying therapies (DMTs), are associated with severe acute respiratory syndrome coronavirus 2 infection severity in people with multiple sclerosis (MS). Comprehensive exploration of these relationships in large international samples is needed. METHODS: Clinician-reported demographic/clinical data from 27 countries were aggregated into a data set of 5,648 patients with suspected/confirmed coronavirus disease 2019 (COVID-19). COVID-19 severity outcomes (hospitalization, admission to intensive care unit [ICU], requiring artificial ventilation, and death) were assessed using multilevel mixed-effects ordered probit and logistic regression, adjusted for age, sex, disability, and MS phenotype. DMTs were individually compared with glatiramer acetate, and anti-CD20 DMTs with pooled other DMTs and with natalizumab. RESULTS: Of 5,648 patients, 922 (16.6%) with suspected and 4,646 (83.4%) with confirmed COVID-19 were included. Male sex, older age, progressive MS, and higher disability were associated with more severe COVID-19. Compared with glatiramer acetate, ocrelizumab and rituximab were associated with higher probabilities of hospitalization (4% [95% CI 1-7] and 7% [95% CI 4-11]), ICU/artificial ventilation (2% [95% CI 0-4] and 4% [95% CI 2-6]), and death (1% [95% CI 0-2] and 2% [95% CI 1-4]) (predicted marginal effects). Untreated patients had 5% (95% CI 2-8), 3% (95% CI 1-5), and 1% (95% CI 0-3) higher probabilities of the 3 respective levels of COVID-19 severity than glatiramer acetate. Compared with pooled other DMTs and with natalizumab, the associations of ocrelizumab and rituximab with COVID-19 severity were also more pronounced. All associations persisted/enhanced on restriction to confirmed COVID-19. DISCUSSION: Analyzing the largest international real-world data set of people with MS with suspected/confirmed COVID-19 confirms that the use of anti-CD20 medication (both ocrelizumab and rituximab), as well as male sex, older age, progressive MS, and higher disability are associated with more severe course of COVID-19.en_US
dc.languageengen_US
dc.relation.ispartofNeurol Neuroimmunol Neuroinflammen_US
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/us/*
dc.subjectAntigens, CD20en_US
dc.subjectCOVID-19en_US
dc.subjectGlatiramer Acetateen_US
dc.subjectHumansen_US
dc.subjectImmunosuppressive Agentsen_US
dc.subjectInformation Disseminationen_US
dc.subjectMaleen_US
dc.subjectMultiple Sclerosisen_US
dc.subjectMultiple Sclerosis, Chronic Progressiveen_US
dc.subjectNatalizumaben_US
dc.subjectRisk Factorsen_US
dc.subjectRituximaben_US
dc.titleUpdated Results of the COVID-19 in MS Global Data Sharing Initiative: Anti-CD20 and Other Risk Factors Associated With COVID-19 Severity.en_US
dc.typeArticle
dc.identifier.doi10.1212/NXI.0000000000200021en_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/36038263en_US
pubs.issue6en_US
pubs.notesNot knownen_US
pubs.publication-statusPublished onlineen_US
pubs.volume9en_US
dcterms.dateAccepted2022-07-27en_US


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Attribution-NonCommercial-NoDerivs 3.0 United States
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 United States