Department of Laboratory Medicine, The Jikei University School of Medicine, Nishishinbashi 3-25-8, Minato-ku, Tokyo, 105-8461, Japan.
The First Department of Internal Medicine, School of Medicine, University of Occupational and Environmental Health, Japan, Iseigaoka1-1, Yahatanishi-ku, Kitakyushu, Fukuoka, 807-8555, Japan.
Arthritis Res Ther. 2024 Jul 26;26(1):140. doi: 10.1186/s13075-024-03369-8.
Rheumatoid arthritis (RA) patients sometimes exhibit different levels of improvement in health assessment questionnaire-disability index (HAQ-DI) and subjective pain visual analogue score (VAS) even after achieving low disease activities (LDA). This study aimed to identify factors associated with improvement in HAQ-DI and pain VAS among those who achieved LDA.
Data of the FIRST registry, a multi-institutional cohort of RA patients treated with biological and targeted-synthetic DMARDs (b/tsDMARDs) were analyzed. Patients who were enrolled from August 2013 to February 2023 and who achieved clinical LDA [clinical disease activity index (CDAI) ≤ 10.0] at 6 months after starting treatment were included. Multiple logistic regression analyses were conducted to identify the factors that associated with achieving HAQ-DI normalization (< 0.5), HAQ-DI improvement (by > 0.22), or pain VAS reduction (≤ 40 mm).
Among 1424 patients who achieved LDA at 6 months, 732 patients achieved HAQ-DI normalization and 454 achieved pain VAS reduction. The seropositivity and the use of JAK inhibitor compared with TNF inhibitor were associated with both HAQ-DI < 0.5 and pain VAS reduction at 6 months. On the other hand, older age, past failure in ≥ 2 classes of b/tsDMARDs, higher HAQ-DI at baseline, and use of glucocorticoid were associated with the lower likelihood of HAQ-DI normalization and pain VAS reduction. Longer disease duration, being female, and higher disease activity at baseline was negatively associated HAQ-DI normalization alone. Comorbidities were not associated with the outcomes.
These results suggest some preferable treatment may exist for improvement of HAQ-DI and pain VAS reduction in the early stage of the treatment, which is a clue to prevention of a criteria of difficult-to-treat RA.
类风湿关节炎(RA)患者在达到低疾病活动度(LDA)后,健康评估问卷残疾指数(HAQ-DI)和主观疼痛视觉模拟评分(VAS)的改善程度有时会存在差异。本研究旨在确定达到 LDA 的患者中,与 HAQ-DI 改善和疼痛 VAS 降低相关的因素。
对 FIRST 登记处的多机构 RA 患者队列的生物和靶向合成 DMARDs(b/tsDMARDs)治疗数据进行了分析。该登记处于 2013 年 8 月至 2023 年 2 月期间入组患者,在治疗开始后 6 个月达到临床 LDA [临床疾病活动指数(CDAI)≤10.0]。进行了多因素逻辑回归分析,以确定与实现 HAQ-DI 正常化(<0.5)、HAQ-DI 改善(增加>0.22)或疼痛 VAS 降低(≤40mm)相关的因素。
在 1424 例 6 个月时达到 LDA 的患者中,732 例达到 HAQ-DI 正常化,454 例达到疼痛 VAS 降低。与 TNF 抑制剂相比,血清阳性和使用 JAK 抑制剂与 6 个月时的 HAQ-DI<0.5 和疼痛 VAS 降低均相关。另一方面,年龄较大、既往使用≥2 类 b/tsDMARDs 失败、基线时 HAQ-DI 较高和使用糖皮质激素与 HAQ-DI 正常化和疼痛 VAS 降低的可能性较低相关。较长的疾病病程、女性和基线时较高的疾病活动度与 HAQ-DI 正常化单独呈负相关。合并症与结局无关。
这些结果表明,在治疗早期可能存在改善 HAQ-DI 和疼痛 VAS 降低的更优治疗方法,这是预防难以治疗的 RA 标准的线索。