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Simplified disease activity changes in real-world practice: a nationwide observational study of seropositive rheumatoid arthritis patients with moderate-to-high disease activityopen access

Authors
Shin, KichulKim, Sung SooLee, Sang-HeonHong, Seung-JaeChoi, Sung JaeChoe, Jung-YoonLee, Seung-GeunCha, Hoon-SukLee, Eun YoungPark, Sung-HwanHur, Jin-WukNa, Sung SooSuh, Chang-HeeSo, Min WookChoi, Seung WonSheen, Dong-HyukPark, WonLee, Shin-SeokRyu, Wan HeeKim, Jin SeokSong, Jung SooLee, Hye SoonKim, Seong HoYoo, Dae-Hyun
Issue Date
Jan-2020
Publisher
대한내과학회
Keywords
Arthritis, rheumatoid; Antirheumatic agents; Biological therapy
Citation
The Korean Journal of Internal Medicine, v.35, no.1, pp 231 - 239
Pages
9
Indexed
SCIE
SCOPUS
KCI
Journal Title
The Korean Journal of Internal Medicine
Volume
35
Number
1
Start Page
231
End Page
239
URI
https://scholarworks.korea.ac.kr/kumedicine/handle/2020.sw.kumedicine/28293
DOI
10.3904/kjim.2018.137
ISSN
1226-3303
2005-6648
Abstract
Background/Aims The objective of this study was to compare changes in the simplified disease activity index (SDAI) between biologic (b) and conventional (c) disease-modifying antirheumatic drugs (DMARD) users with seropositive rheumatoid arthritis (RA) in daily clinical practice. Methods This was a nationwide multicenter observational study. Patients who had three or more active joint counts and abnormal inf lammatory marker in blood test were enrolled. The selection of DMARDs was determined by the attending rheumatologist. Clinical parameters, laboratory findings, and Health Assessment Questionnaire (HAQ) scores were obtained at baseline and at 6 and 12 months. Serial SDAI changes and clinical remission rate at 6 and 12 months were assessed. Results A total of 850 patients participated in this study. The mean baseline SDAI score in bDMARD group was higher than that in cDMARD group (32.08 ± 12.98 vs 25.69 ± 10.97, p < 0.0001). Mean change of SDAI at 12 months was –19.0 in the bDMARD group and –12.6 in the cDMARD group (p < 0.0001). Clinical remission rates at 12 months in bDMARD and cDMARD groups were 15.4% and 14.6%, respectively. Patient global assessment and HAQ at 12 months were also significantly improved in both groups. Multivariate logistic regression showed that baseline HAQ score was the most notable factor associated with remission. Conclusions There was a significant reduction in SDAI within 12 months after receiving DMARDs in Korean seropositive RA patients irrespective of bDMARD or cDMARD use in real-world practice. Clinical remission was achieved in those with lower baseline HAQ scores.
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