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dc.contributor.author정성애*
dc.contributor.author정혜경*
dc.contributor.author심기남*
dc.contributor.author김성은*
dc.contributor.author문창모*
dc.contributor.author송은미*
dc.contributor.author안형미*
dc.date.accessioned2026-04-06T16:30:01Z-
dc.date.available2026-04-06T16:30:01Z-
dc.date.issued2026*
dc.identifier.issn0022-1899*
dc.identifier.otherOAK-39173*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/274991-
dc.description.abstractBackground. The role of biologics and small molecules in coronavirus disease 2019 (COVID-19) risk remains unclear. Therefore, we aimed to evaluate COVID-19 risk among patients with systemic autoimmune diseases treated with biologics or small molecules using the population-based cohort in Korea. Methods. We compared COVID-19 risk in 46 639 patients treated with biologics or small molecules (biologics group) to a 1:2 propensity score–matched (PSM) group of 86 980 controls (nonbiologics group). We matched the groups based on age, sex, type of autoimmune disease, Charlson Comorbidity Index, concurrent medications, and pre-COVID-19 vaccine doses. Results. After PSM, the biologics group exhibited a significantly higher COVID-19 risk (adjusted odds ratio [aOR], 1.20 [95% confidence interval {CI}, 1.08–1.34]) than the nonbiologics group. Subgroup analysis revealed a significant increase in COVID-19 risk in the biologics group that received suboptimal vaccines (aOR, 1.20 [95% CI, 1.08–1.34]). However, under optimal vaccine administration (3–4 doses), the risk of COVID-19 did not differ significantly between the biologics and nonbiologics groups (aOR, 1.22 [95% CI,.74–2.00]). Furthermore, COVID-19 risk significantly increased in patients with anti–tumor necrosis factor agents (aOR, 1.20 [95% CI, 1.05–1.36]), tofacitinib (aOR, 1.76 [95% CI, 1.15–2.71]), and abatacept (aOR, 1.98 [95% CI, 1.11–3.50]), compared with nonusers. Conclusions. Among patients with systemic autoimmune diseases, the risk of COVID-19 was significantly higher in those taking biologics or small molecules than in those not taking biologics. When receiving suboptimal COVID-19 vaccination, the risk of COVID-19 significantly increased in the biologics compared to the nonbiologics group, but it was mitigated through optimal vaccinations. © The Author(s) 2025. Published by Oxford University Press on behalf of Infectious Diseases Society of America. All rights reserved.*
dc.description.sponsorshipOxford University Press*
dc.languageEnglish*
dc.subjectautoimmune disease*
dc.subjectbiologics*
dc.subjectCOVID-19*
dc.subjectsmall molecules*
dc.subjectvaccine*
dc.titleCoronavirus Disease 2019 Risk in Patients With Autoimmune Diseases Using Biologics or Small Molecules: A Population-Based Cohort Study*
dc.typeArticle*
dc.relation.issue1*
dc.relation.volume233*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage137*
dc.relation.lastpage147*
dc.relation.journaltitleJournal of Infectious Diseases*
dc.identifier.doi10.1093/infdis/jiaf347*
dc.identifier.wosidWOS:001529423300001*
dc.identifier.scopusid2-s2.0-105027743947*
dc.author.googleSong E.M.*
dc.author.googleAn H.-M.*
dc.author.googleKim S.-E.*
dc.author.googleShim K.-N.*
dc.author.googleJung H.-K.*
dc.author.googleJung S.-A.*
dc.author.googleMoon C.M.*
dc.contributor.scopusid정성애(7403676915;60607776000)*
dc.contributor.scopusid정혜경(7403029723)*
dc.contributor.scopusid심기남(13604838300)*
dc.contributor.scopusid김성은(57204243828;58712383600;59006249300;60157921200;)*
dc.contributor.scopusid문창모(8131765500)*
dc.contributor.scopusid송은미(57193312165)*
dc.contributor.scopusid안형미(59438825300;56044098700)*
dc.date.modifydate20261013120834*
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의과대학 > 의학과 > Journal papers
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