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dc.contributor.author성윤경-
dc.date.accessioned2019-09-30T01:00:22Z-
dc.date.available2019-09-30T01:00:22Z-
dc.date.issued2019-04-
dc.identifier.citationPLOS ONE, v. 14, NO 4, no. e0214981en_US
dc.identifier.issn1932-6203-
dc.identifier.urihttps://journals.plos.org/plosone/article?id=10.1371/journal.pone.0214981-
dc.identifier.urihttps://repository.hanyang.ac.kr/handle/20.500.11754/110741-
dc.description.abstractObjective Remission is a key goal in managing rheumatoid arthritis (RA), with sustained remission as the preferred sequelae of short-term remission. However little is known about the predictors of sustained remission for patients reaching remission. Using two independent cohorts, we aimed to evaluate the prevalence and predictors for sustained remission. Methods The study cohort consisted of subjects with RA from the Brigham and Women's Hospital Rheumatoid Arthritis Sequential Study (BRASS) and the Korean Observational Study Network for Arthritis (KORONA). We analyzed subjects who reached remission in 2009 with follow up data for two consecutive years. Remission was defined by the Disease Activity Score 28-(DAS28-CRP) of less than 2.6. Sustained remission was defined as three consecutive annual visits in remission. Predictors for sustained remission were identified by multivariate logistic regression analysis. Results A total of 465 subjects were in remission in 2009. Sustained remission was achieved by 53 of 92 (57.5%) in BRASS and by 198 of 373 (53.1%) in KORONA. In multivariate analyses, baseline predictors of sustained remission were: disease duration less than 5 years [odds ratio (OR) 1.96, 95% confidence interval (95% CI) 1.08-3.58], Modified Health Assessment Questionnaire (MHAQ) score of 0 (OR 1.80, 95% CI 1.18-2.74), and non-use of oral glucocorticoid (OR 1.58, 95% CI 1.01-2.47). Conclusion More than half of RA subjects in remission in 2009 remained in remission through 2011. Short disease duration, no disability, and non-use of oral glucocorticoid at baseline were associated with sustained remission.en_US
dc.description.sponsorshipThis study received no specific support. However, BRASS is supported by grants from Crescendo Biosciences, Medimmune, Briston Myers Squibb. KORONA receives support from the Korea Healthcare technology R&D Project, Ministry for Health and Welfare, Republic of Korea (A102065). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.en_US
dc.language.isoenen_US
dc.publisherPUBLIC LIBRARY SCIENCEen_US
dc.subjectDISEASE-ACTIVITYen_US
dc.subjectPROGNOSTIC-FACTORSen_US
dc.subjectCRITERIAen_US
dc.subjectCOHORTen_US
dc.subjectRESEARCHERSen_US
dc.subjectCONSORTIUMen_US
dc.subjectOUTCOMESen_US
dc.subjectDAS28en_US
dc.subjectSEXen_US
dc.titlePrevalence and predictors for sustained remission in rheumatoid arthritisen_US
dc.typeArticleen_US
dc.relation.no4-
dc.relation.volume14-
dc.identifier.doi10.1371/journal.pone.0214981-
dc.relation.page1-10-
dc.relation.journalPLOS ONE-
dc.contributor.googleauthorSung, Yoon-Kyoung-
dc.contributor.googleauthorYoshida, Kazuki-
dc.contributor.googleauthorPrince, Femke H. M.-
dc.contributor.googleauthorFrits, Michelle L.-
dc.contributor.googleauthorCho, Soo-Kyung-
dc.contributor.googleauthorChoe, Jung-Yoon-
dc.contributor.googleauthorLee, Hye-Soon-
dc.contributor.googleauthorLee, Jisoo-
dc.contributor.googleauthorLee, Shin-Seok-
dc.contributor.googleauthorYoo, Dae-Hyun-
dc.relation.code2019042142-
dc.sector.campusS-
dc.sector.daehakCOLLEGE OF MEDICINE[S]-
dc.sector.departmentDEPARTMENT OF MEDICINE-
dc.identifier.pidsungyk-
dc.identifier.orcidhttps://orcid.org/0000-0001-6691-8939-


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