Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/47477
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dc.contributor.authorSen S.-
dc.contributor.authorTuncer A.-
dc.contributor.authorOzakbas S.-
dc.contributor.authorUzunkopru C.-
dc.contributor.authorBaba C.-
dc.contributor.authorDemir S.-
dc.contributor.authorBeckmann Y.-
dc.contributor.authorBir, Levent Sinan-
dc.contributor.authorGumus, Haluk-
dc.contributor.authorArslan, Gokhan-
dc.contributor.authorKilic, Ahmet Kasim-
dc.contributor.authorAltintas, Ayse-
dc.contributor.authorYuceyar, Nur-
dc.contributor.authorTuran, Omer Faruk-
dc.contributor.authorTutuncu, Melih-
dc.contributor.authorTerzi, Murat-
dc.contributor.authorAcar, Pinar-
dc.contributor.authorBunul, Sena Destan-
dc.contributor.authorBalci, Belgin Petek-
dc.contributor.authorKoseoglu, Mesrure-
dc.contributor.authorMungan, Semra-
dc.contributor.authorGunduz, Tuncay-
dc.contributor.authorDogan, Ipek Gungor-
dc.contributor.authorKotan, Dilcan-
dc.contributor.authorUygunoglu, Ugur-
dc.contributor.authorEkmekci, Ozgul-
dc.contributor.authorDemirkiran, Meltem-
dc.contributor.authorKamisli, Ozden-
dc.contributor.authorKabay, Sibel Canbaz-
dc.contributor.authorTamam, Yusuf-
dc.contributor.authorOmerhoca, Sami-
dc.contributor.authorSevim, Serhan-
dc.contributor.authorGuler, Sibel-
dc.contributor.authorKurtuncu, Murat-
dc.contributor.authorEfendi, Husnu-
dc.contributor.authorKarabudak, Rana-
dc.contributor.authorSiva, Aksel-
dc.date.accessioned2023-01-09T21:24:54Z-
dc.date.available2023-01-09T21:24:54Z-
dc.date.issued2022-
dc.identifier.issn2211-0348-
dc.identifier.urihttps://doi.org/10.1016/j.msard.2021.103399-
dc.identifier.urihttps://hdl.handle.net/11499/47477-
dc.description.abstractBackground: COVID-19 is a multisystemic infection with variables consequences depending on individual and comorbid conditions. The course and outcomes of COVID-19 during neuromyelitis optica spectrum disorders (NMOSD) and myelin oligodendrocyte glycoprotein antibody-associated disorders (MOGAD) are not clearly known. Objective/methods: The aim of this study was to examine the features and outcomes of COVID-19 infection in NMOSD and MOGAD patients. The patients' demographic and clinical factors, disease modifying treatment (DMT) used and disease information of COVID-19 infection were recorded. Conditions leading to hospitalization and severe exposure to COVID-19 infection were also analyzed. Results: The study included 63 patients from 25 centers. Thirty-two patients (50.8%) belong to AQP-4 seropositive group, 13 (20.6%) and 18 (28.6%) were in MOG-positive and double-seronegative groups, respectively. Risk factors for severe COVID-19 infection and hospitalization were advanced age, high disability level and the presence of comorbid disease. Disease severity was found to be high in double-seronegative NMOSD and low in MOGAD patients. No statistically significant effect of DMTs on disease severity and hospitalization was found. Conclusion: In NMOSD and MOGAD patients, advanced age, high disability and presence of comorbid disease pose risks for severe COVID-19 infection. There was no direct significant effect of DMTs for COVID-19 infection. © 2021 Elsevier B.V.en_US
dc.language.isoenen_US
dc.publisherElsevier B.V.en_US
dc.relation.ispartofMultiple Sclerosis and Related Disordersen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectCoronavirusen_US
dc.subjectDisease modifying treatmenten_US
dc.subjectMyelin oligodendrocyte glycoprotein antibody-associated disordersen_US
dc.subjectNeuromyelitis optica spectrum disordersen_US
dc.subjectSARS-CoV-2en_US
dc.subjectazathioprineen_US
dc.subjectmyelin oligodendrocyte glycoproteinen_US
dc.subjectrituximaben_US
dc.subjectaquaporin 4en_US
dc.subjectautoantibodyen_US
dc.subjectmyelin oligodendrocyte glycoproteinen_US
dc.subjectadulten_US
dc.subjectageen_US
dc.subjectArticleen_US
dc.subjectclinical featureen_US
dc.subjectclinical outcomeen_US
dc.subjectcohort analysisen_US
dc.subjectcomorbidityen_US
dc.subjectcontrolled studyen_US
dc.subjectcoronavirus disease 2019en_US
dc.subjectdeathen_US
dc.subjectdisease associationen_US
dc.subjectdisease durationen_US
dc.subjectdisease severityen_US
dc.subjectexperienceen_US
dc.subjectexposureen_US
dc.subjectfemaleen_US
dc.subjecthospitalizationen_US
dc.subjecthumanen_US
dc.subjectmajor clinical studyen_US
dc.subjectmaleen_US
dc.subjectmedical informationen_US
dc.subjectmyelin oligodendrocyte glycoprotein antibody associated disorderen_US
dc.subjectmyelooptic neuropathyen_US
dc.subjectprotein deficiencyen_US
dc.subjectrisk factoren_US
dc.subjectserologyen_US
dc.subjectcomplicationen_US
dc.subjectmyelooptic neuropathyen_US
dc.subjectAquaporin 4en_US
dc.subjectAutoantibodiesen_US
dc.subjectCOVID-19en_US
dc.subjectHumansen_US
dc.subjectMyelin-Oligodendrocyte Glycoproteinen_US
dc.subjectNeuromyelitis Opticaen_US
dc.subjectSARS-CoV-2en_US
dc.titleThe Turkish experience of COVID-19 infection in people with NMOSD and MOGAD: A milder course?en_US
dc.typeArticleen_US
dc.identifier.volume58en_US
dc.identifier.doi10.1016/j.msard.2021.103399-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.authorscopusid56042671700-
dc.authorscopusid57195979263-
dc.authorscopusid6602895100-
dc.authorscopusid37666211300-
dc.authorscopusid57217015818-
dc.authorscopusid56450290500-
dc.authorscopusid35095964200-
dc.identifier.pmid35216782en_US
dc.identifier.scopus2-s2.0-85122957692en_US
dc.identifier.wosWOS:000793561600010en_US
dc.identifier.scopusqualityQ1-
item.languageiso639-1en-
item.openairetypeArticle-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.dept14.02. Internal Medicine-
crisitem.author.dept14.02. Internal Medicine-
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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