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老年发病型类风湿关节炎(EORA)与非老年发病型老年患者对生物制剂应答的相似性:来自 FIRST 登记研究。

Similarity of Response to Biologics Between Elderly-onset Rheumatoid Arthritis (EORA) and Non-EORA Elderly Patients: From the FIRST Registry.

机构信息

S. Ochi, PhD, Department of Laboratory Medicine, The Jikei University School of Medicine, Tokyo, and the First Department of Internal Medicine, School of Medicine, University of Occupational and Environmental Health, Kitakyushu.

F. Mizoguchi, PhD, Department of Rheumatology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University (TMDU), Tokyo.

出版信息

J Rheumatol. 2021 Nov;48(11):1655-1662. doi: 10.3899/jrheum.201135. Epub 2021 Feb 15.

Abstract

OBJECTIVE

Increasing numbers of patients are developing rheumatoid arthritis (RA) at an older age, and optimal treatment of patients with elderly-onset RA (EORA) is attracting greater attention. This study aimed to analyze the efficacy and safety of biologic/targeted synthetic disease-modifying antirheumatic drugs (b/tsDMARDs) in EORA and non-EORA elderly patients.

METHODS

A cohort of patients with RA treated with b/tsDMARDs were retrospectively analyzed. Only patients aged ≥ 60 years were included. Among them, patients who developed RA aged ≥ 60 years were categorized as EORA, whereas those aged < 60 years were categorized as non-EORA elderly. Disease activity was compared between the EORA and non-EORA elderly groups.

RESULTS

In total, 1040 patients were categorized as EORA and 710 as non-EORA elderly. There were no significant differences in characteristics at baseline between the 2 groups. The proportion of patients with low and high disease activity was comparable at Weeks 2, 22, and 54 between the EORA and the non-EORA elderly group. There were no significant differences in the reasons for the discontinuation of b/tsDMARDs between the 2 groups. Elderly RA onset did not affect changes in Clinical Disease Activity Index (CDAI) and Health Assessment Questionnaire-Disability Index, nor did it affect the reasons for b/tsDMARD discontinuation between the 2 groups. The trajectory analysis on CDAI responses to b/tsDMARDs for 54 weeks identified 3 response patterns. The proportion of patients categorized into each group and CDAI response trajectories to b/tsDMARDs were very similar between EORA and non-EORA elderly patients.

CONCLUSION

CDAI response patterns to b/tsDMARDs and HR of adverse events were similar between EORA and non-EORA elderly patients.

摘要

目的

越来越多的患者在老年时出现类风湿关节炎(RA),因此老年发病的 RA(EORA)患者的最佳治疗方案受到了更多关注。本研究旨在分析生物/靶向合成的疾病修饰抗风湿药物(b/tsDMARDs)在 EORA 和非老年 EORA 患者中的疗效和安全性。

方法

回顾性分析了接受 b/tsDMARDs 治疗的 RA 患者队列。仅纳入年龄≥60 岁的患者。其中,年龄≥60 岁发病的患者被归类为 EORA,而年龄<60 岁的患者归类为非老年 EORA。比较 EORA 和非老年 EORA 组之间的疾病活动度。

结果

共纳入 1040 例 EORA 和 710 例非老年 EORA 患者。两组患者的基线特征无显著差异。在第 2、22 和 54 周时,EORA 和非老年 EORA 组的低疾病活动度和高疾病活动度患者比例相当。两组患者因 b/tsDMARD 停药的原因无显著差异。老年 RA 发病不影响 CDAI 的变化和健康评估问卷残疾指数,也不影响两组患者因 b/tsDMARD 停药的原因。对 b/tsDMARD 治疗 54 周的 CDAI 反应进行轨迹分析,共确定了 3 种反应模式。EORA 和非老年 EORA 患者中,归入各亚组的患者比例和 CDAI 对 b/tsDMARDs 的反应轨迹非常相似。

结论

EORA 和非老年 EORA 患者对 b/tsDMARDs 的 CDAI 反应模式和不良事件的 HR 相似。

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