Publication:
The Impact of COVID-19 Infection on Multiple Sclerosis Disease Course across 12 Countries: A Propensity-Score Cohort Study

dc.authorwosidWillekens, Barbara/Aaw-1790-2021
dc.authorwosidOzakbas, Serkan/V-6427-2019
dc.authorwosidAlhrbi, Talal/Act-2101-2022
dc.authorwosidFoschi, Matteo/Abr-7231-2022
dc.authorwosidKarabudak, Rana/Hjh-2490-2023
dc.authorwosidBlanco, Yolanda/Oir-7874-2025
dc.authorwosidSoysal, Aysun/Aax-7696-2021
dc.contributor.authorLevitz, David
dc.contributor.authorFoong, Yi Chao
dc.contributor.authorSanfilippo, Paul
dc.contributor.authorSpelman, Tim
dc.contributor.authorRath, Louise
dc.contributor.authorRoldan, Angie
dc.contributor.authorVan Der Walt, Anneke
dc.contributor.authorIDJokubaitis, Vilija/0000-0002-3942-4340
dc.contributor.authorIDWillekens, Barbara/0000-0002-5212-8837
dc.contributor.authorIDLal, Anoushka/0000-0001-5273-7475
dc.contributor.authorIDSurcinelli, Anea/0000-0003-3779-0934
dc.contributor.authorIDLevitz, David/0009-0008-3610-1926
dc.contributor.authorIDZhu, Chao/0000-0003-3951-7501
dc.date.accessioned2025-12-11T01:39:30Z
dc.date.issued2024
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Van Der Walt, Anneke] Monash Univ, Cent Clin Sch, Dept Neurosci, 99 Commercial Rd, Melbourne, Vic 3004, Australia; [Foong, Yi Chao; Skibina, Olga; Butzkueven, Helmut; Van Der Walt, Anneke] Alfred Hosp, Dept Neurol, Melbourne, Vic, Australia; [Levitz, David; Foong, Yi Chao; Sanfilippo, Paul; Roldan, Angie; Lal, Anoushka; Monif, Mastura; Jokubaitis, Vilija; Zhu, Chao; Gresle, Melissa; Butzkueven, Helmut] Monash Univ, Cent Clin Sch, Dept Neurosci, Melbourne, Vic, Australia; [Spelman, Tim] Karolinska Inst, Dept Clin Neurosci, Stockholm, Sweden; [Ozakbas, Serkan] Dokuz Eylul Univ, Konak, Turkiye; [Alroughani, Raed] Amiri Hosp, Dept Med, Div Neurol, Kuwait, Kuwait; [Boz, Cavit] Farabi Hosp, KTU Med Fac, Trabzon, Turkiye; [Terzi, Murat] 19 Mayis Univ, Med Fac, Samsun, Turkiye; [Kalincik, Tomas] Royal Melbourne Hosp, Neuroimmunol Ctr, Dept Neurol, Melbourne, Vic, Australia; [Kalincik, Tomas] Univ Melbourne, Dept Med, CORe, Melbourne, Vic, Australia; [Blanco, Yolanda] Hosp Clin Barcelona, Ctr Neuroimmunol, Serv Neurol, Barcelona, Spain; [Foschi, Matteo; Surcinelli, Andrea] S Maria Croci Hosp Ravenna, AUSL Romagna, Dept Neurosci, Neurol Unit, Ravenna, Italy; [Foschi, Matteo] Univ LAquila, Dept Biotechnol & Appl Clin Sci DISCAB, Laquila, Italy; [Buzzard, Katherine; Skibina, Olga; Merlo, Daniel] Box Hill Hosp, Dept Neurol, Melbourne, Vic, Australia; [Buzzard, Katherine; Skibina, Olga] Monash Univ, Eastern Hlth Clin Sch, Box Hill, Vic, Australia; [Laureys, Guy; Van Hijfte, Liesbeth] Univ Hosp Ghent, Dept Neurol, Ghent, Belgium; [Ramo-Tello, Cristina] Hosp Germans Trias i Pujol, Badalona, Spain; [Soysal, Aysun] Bakirkoy Educ & Res Hosp Psychiat & Neurol Dis, Istanbul, Turkiye; [Sanchez-Menoyo, Jose Luis] Hosp Galdakao Usansolo, Galdakao, Spain; [Sanchez-Menoyo, Jose Luis] Inst Invest Sanitario Biocruces Bizkaia, Baracaldo, Spain; [Habek, Mario] Univ Hosp Ctr Zagreb, Dept Neurol, Zagreb, Croatia; [Habek, Mario] Univ Zagreb, Sch Med, Zagreb, Croatia; [Cartechini, Elisabetta] Azienda Sanit Unica Reg Marche AV3, UOC Neurol, Macerata, Italy; [Rojas, Juan Ignacio] Hosp Univ CEMIC, Buenos Aires, Argentina; [Karabudak, Rana] Hacettepe Univ, Ankara, Turkiye; [Willekens, Barbara] Antwerp Univ Hosp, Dept Neurol, Edegem, Belgium; [Willekens, Barbara] Univ Antwerp, Fac Med & Hlth Sci, Translat Neurosci Res Grp, Antwerp, Belgium; [Al-Harbi, Talal] King Fahad Specialist Hosp Dammam, Dammam, Saudi Arabia; [Fragoso, Yara] Univ Metropolitana Santos, Santos, Brazil; [Castillo-Trivino, Tamara] Hosp Univ Donostia, San Sebastian, Spain; [Castillo-Trivino, Tamara] IIS Biodonostia, San Sebastian, Spain; [Decoo, Danny] AZ Alma Ziekenhuis, Damme, Belgium; [de Vecino, Maria Cecilia Aragon] Hosp Moinhos Vento, Porto Alegre, Brazil; [Skromne, Eli] Inst Mexicano Neurociencias, Hosp Angeles Las Lomas, Huixquilucan, Mexico; [Sirbu, Carmen-Adella] Cent Mil Emergency Univ Hosp, Bucharest, Romania; [Sirbu, Carmen-Adella] Titu Maiorescu Univ, Bucharest, Romaniaen_US
dc.descriptionJokubaitis, Vilija/0000-0002-3942-4340; Willekens, Barbara/0000-0002-5212-8837; Lal, Anoushka/0000-0001-5273-7475; Surcinelli, Anea/0000-0003-3779-0934; Levitz, David/0009-0008-3610-1926; Zhu, Chao/0000-0003-3951-7501; Foong, Yi Chao/0000-0001-6447-078X; Sirbu, Carmen Adella/0000-0002-1982-1066; Foschi, Matteo/0000-0002-0321-7155;en_US
dc.description.abstractBackground: The relationship between coronavirus disease 2019 (COVID-19) infection and multiple sclerosis (MS) relapse and disease progression remains unclear. Previous studies are limited by small sample sizes and most lack a propensity-matched control cohort.Objective: To evaluate the effect of COVID-19 infection on MS disease course with a large propensity-matched cohort.Design: This multi-centre cohort study analysed relapse and disability outcomes post-COVID-19 infection after balancing covariates using a propensity score matching method. The study period was from the 11th of September 2019 to the 16th of February 2023. The mean follow-up period was 1.7 years.Methods: Data were retrieved from the MSBase Registry. Propensity scores were obtained based on age, sex, disease duration, baseline Expanded Disability Status Scale (EDSS), MS course, relapses pre-baseline, disease-modifying therapy (DMT) class and country. Primary outcomes were time to first relapse, annualised relapse rate (ARR) and time to confirm EDSS progression. Secondary outcomes were time to EDSS of 3, 4 or 6. Sensitivity analyses with baseline DMT classes were performed.Results: The study included 2253 cases and 6441 controls. After matching, there were 2161 cases and an equal number of matched controls. Cases had a significantly higher ARR (ARR = 0.10 [95% CI 0.09-0.11]) compared to controls (ARR = 0.07 [95% CI 0.06-0.08]). Cases had a significantly greater hazard of time to first relapse compared to controls (hazard ratio (HR) = 1.54 [95% CI 1.29-1.84]). There was no association between COVID-19 infection and 24-week EDSS progression (HR = 1.18 [95% CI 0.92-1.52]), or time to EDSS of 3, 4 or 6. For patients on interferons and glatiramer acetate (BRACE), COVID-19 infection was associated with a greater hazard of time to first relapse (HR = 1.83 [95% CI 1.25-2.68]) and greater hazard of time to EDSS of 3 (HR = 2.04 [95% CI 1.06-3.90]) compared to patients on BRACE therapy without COVID-19 infection.Conclusion: COVID-19 infection was associated with a significantly increased MS relapse rate and a shorter time to first relapse. There was no effect on confirmed EDSS progression over the short term. These results support ongoing COVID-19 risk minimisation strategies to protect patients with MS.en_US
dc.description.woscitationindexScience Citation Index Expanded
dc.identifier.doi10.1177/17562864241278496
dc.identifier.issn1756-2856
dc.identifier.issn1756-2864
dc.identifier.pmid39525878
dc.identifier.scopusqualityQ1
dc.identifier.urihttps://doi.org/10.1177/17562864241278496
dc.identifier.urihttps://hdl.handle.net/20.500.12712/45216
dc.identifier.volume17en_US
dc.identifier.wosWOS:001349951500001
dc.identifier.wosqualityQ1
dc.language.isoenen_US
dc.publisherSage Publications Ltden_US
dc.relation.ispartofTherapeutic Advances in Neurological Disordersen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectCOVID-19en_US
dc.subjectDisease Progressionen_US
dc.subjectMultiple Sclerosisen_US
dc.subjectRelapseen_US
dc.titleThe Impact of COVID-19 Infection on Multiple Sclerosis Disease Course across 12 Countries: A Propensity-Score Cohort Studyen_US
dc.typeArticleen_US
dspace.entity.typePublication

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