Contributing factors of clinical outcomes at 1 year post-diagnosis in early rheumatoid arthritis patients with tightly controlled disease activity in clinical practice: a retrospective study

医学 类风湿性关节炎 内科学 类风湿因子 滑膜炎 甲氨蝶呤 痹症科 回顾性队列研究 物理疗法
作者
Shin‐ya Kawashiri,Yushiro Endo,Momoko Okamoto,Sosuke Tsuji,Toshimasa Shimizu,Remi Sumiyoshi,Tomohiro Koga,Naoki Iwamoto,Kunihiro Ichinose,Mami Tamai,Hideki Nakamura,Tomoki Origuchi,Atsushi Kawakami
出处
期刊:Modern Rheumatology [Informa]
卷期号:31 (2): 343-349 被引量:3
标识
DOI:10.1080/14397595.2020.1795392
摘要

To determine whether specific parameters contribute to clinical outcomes at 1 year post-diagnosis in early rheumatoid arthritis (RA) patients under the 'treat-to-target' strategy in clinical practice.We retrospectively analyzed 125 RA patients selected according to the following criteria; the patients' symptom duration was ≤6 months, and none had experience with DMARDs. We evaluated the patients' clinical disease activity at baseline and 1 year of treatment and the musculoskeletal ultrasound (MSUS)-detected synovitis activity at baseline. We performed an analysis to identify parameters that contribute to SDAI remission and the use of biologic/targeted synthetic (b/ts) DMARDs at 1 year post-diagnosis.Forty-seven patients received b/tsDMARDs therapy, and 58 patients achieved SDAI remission at 1 year post-diagnosis. Rheumatoid factor positivity, low patient's/evaluator's global assessment at baseline, and methotrexate use at 1 year post-diagnosis were associated with SDAI remission. The baseline clinical disease activity and MSUS scores were not associated with SDAI remission. Anti-cyclic citrullinated peptide antibody positivity/high titer and high swollen joint counts or the presence of severe synovial hypertrophy at baseline were associated with the use of b/tsDMARDs therapy.The value of the expected poor-prognosis factors may be diminished by intensive therapy within the 'windows of opportunity'.

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