Departments of Community Medicine, Nagasaki University Graduate School of Medical Sciences, Nagasaki, Japan.
Immunology and Rheumatology, Division of Advanced Preventive Medical Sciences, Nagasaki University Graduate School of Medical Sciences, Nagasaki, Japan.
Mod Rheumatol. 2021 Mar;31(2):343-349. doi: 10.1080/14397595.2020.1795392. Epub 2020 Jul 31.
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'.
在“达标治疗”策略下,确定特定参数是否有助于早期类风湿关节炎(RA)患者在诊断后 1 年内的临床结局。
我们回顾性分析了 125 例符合以下标准的 RA 患者;患者的症状持续时间≤6 个月,且均无 DMARDs 治疗史。我们评估了患者在基线和治疗 1 年时的临床疾病活动度以及基线时的肌肉骨骼超声(MSUS)检测到的滑膜炎活动度。我们进行了一项分析,以确定在诊断后 1 年内与 SDAI 缓解和使用生物/靶向合成(b/ts)DMARDs 相关的参数。
47 例患者接受了 b/tsDMARD 治疗,58 例患者在诊断后 1 年内达到了 SDAI 缓解。基线时类风湿因子阳性、患者/评估者全球评估低、以及在诊断后 1 年内使用甲氨蝶呤与 SDAI 缓解相关。基线临床疾病活动度和 MSUS 评分与 SDAI 缓解无关。基线时抗环瓜氨酸肽抗体阳性/高滴度和高肿胀关节计数或存在严重滑膜肥厚与使用 b/tsDMARDs 治疗相关。
在“机会之窗”内进行强化治疗可能会降低预期不良预后因素的价值。