| dc.contributor | Vall d'Hebron Barcelona Hospital Campus |
| dc.contributor.author | Simpson-Yap, Steve |
| dc.contributor.author | Pirmani, Ashkan |
| dc.contributor.author | Kalincik, Tomas |
| dc.contributor.author | De Brouwer, Edward |
| dc.contributor.author | Geys, Lotte |
| dc.contributor.author | Parciak, Tina |
| dc.contributor.author | Zabalza de Torres, Ana |
| dc.contributor.author | Arrambide, Georgina |
| dc.date.accessioned | 2022-11-10T07:19:16Z |
| dc.date.available | 2022-11-10T07:19:16Z |
| dc.date.issued | 2022-11 |
| dc.identifier.citation | Simpson-Yap S, Pirmani A, Kalincik T, De Brouwer E, Geys L, Parciak T, et al. Updated Results of the COVID-19 in MS Global Data Sharing Initiative. Neurol Neuroimmunol Neuroinflamm. 2022 Nov;9(6):e200021. |
| dc.identifier.issn | 2332-7812 |
| dc.identifier.uri | https://hdl.handle.net/11351/8427 |
| dc.description | COVID-19; Severe acute respiratory syndrome; Data set |
| dc.description.abstract | Background 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. |
| dc.language.iso | eng |
| dc.publisher | Lippincott, Williams & Wilkins |
| dc.relation.ispartofseries | Neurology, Neuroimmunology and Neuroinflammation;9(6) |
| dc.rights | Attribution-NonCommercial-NoDerivatives 4.0 International |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ |
| dc.source | Scientia |
| dc.subject | Esclerosi múltiple |
| dc.subject | COVID-19 (Malaltia) - Factors de risc |
| dc.subject.mesh | Multiple Sclerosis |
| dc.subject.mesh | Coronavirus Infections |
| dc.subject.mesh | Risk Factors |
| dc.title | Updated Results of the COVID-19 in MS Global Data Sharing Initiative: Anti-CD20 and Other Risk Factors Associated With COVID-19 Severity |
| dc.type | info:eu-repo/semantics/article |
| dc.identifier.doi | 10.1212/NXI.0000000000200021 |
| dc.subject.decs | esclerosis múltiple |
| dc.subject.decs | infecciones por Coronavirus |
| dc.subject.decs | factores de riesgo |
| dc.relation.publishversion | https://doi.org/10.1212/NXI.0000000000200021 |
| dc.type.version | info:eu-repo/semantics/publishedVersion |
| dc.audience | Professionals |
| dc.contributor.organismes | Institut Català de la Salut |
| dc.contributor.authoraffiliation | [Simpson-Yap S] CORe, Department of Medicine, and Neuroepidemiology Unit, Melbourne School of Population & Global Health, The University of Melbourne, Menzies Institute for Medical Research, University of Tasmania, Australia. [Pirmani A, Geys L, Parciak T] ESAT-STADIUS, KU Leuven, Biomedical Research Institute–Data Science Institute, Hasselt University, Belgium. [Kalincik T] CORe, Department of Medicine, The University of Melbourne, MS Centre, Department of Neurology, Royal Melbourne Hospital, Australia. [De Brouwer E] ESAT-STADIUS, KU Leuven, Belgium. [Zabalza de Torres A, Arrambide G] Servei de Neurologia-Neuroimmunologia, Centre d’Esclerosi Múltiple de Catalunya (CEMCAT), Barcelona, Spain. Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. Vall d’Hebron Hospital Universitari, Barcelona, Spain. Universitat Autònoma de Barcelona, Bellaterra, Spain |
| dc.identifier.pmid | 36038263 |
| dc.rights.accessrights | info:eu-repo/semantics/openAccess |