The impact of aging and glucocorticoid use on physical function of older rheumatoid arthritis in remission: analysis of a National Database of Rheumatic Disease in Japan.

IF 2.8 3区 医学 Q2 RHEUMATOLOGY
Clinical Rheumatology Pub Date : 2025-09-01 Epub Date: 2025-07-30 DOI:10.1007/s10067-025-07599-2
Yoji Komiya, Takahiko Sugihara, Tatsuro Ishizaki, Naoki Kimura, Mari Kamiya, Fumio Hirano, Takumi Matsumoto, Hirokazu Sasaki, Tadashi Hosoya, Shigeto Tohma, Shinsuke Yasuda, Toshihiro Matsui
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引用次数: 0

Abstract

Objective: To investigate clinical features and physical function in rheumatoid arthritis (RA) in remission with and without glucocorticoid (GC).

Methods: Data from 2078 RA patients aged 55-84 years in remission (simplified disease activity index (SDAI) ≤ 3.3) and at stage I/II according to the Steinbrocker classification were extracted from the National Database of Rheumatic Diseases in Japan (NinJa) which includes 11,036 patients from 2017 to 2018 before the coronavirus pandemic. Patients were stratified into six groups: RA aged 55-64, aged 65-74, and aged 75-84 with or without GCs. The primary outcome was the health assessment questionnaire disability index (HAQ-DI) > 0.5, and interactions of age and GC use on the HAQ-DI > 0.5 were examined by multivariable logistic regression.

Results: GC use in patients in remission increased with age. Methotrexate and biological disease-modifying antirheumatic drug prescriptions were similar in patients aged 75-84 with and without GC. Significantly more GC users aged 75-84, but not aged 65-74 and 55-64, had a HAQ-DI > 0.5 than GC non-users (23.9% vs. 14.8%, P = 0.015). An interaction between age and GC use for HAQ-DI > 0.5 was observed, and the adjusted odds ratios (ORs) relative to GC non-users aged 55-64 for HAQ-DI > 0.5 increased to 4.72 (95% CI 2.49-8.96, P < 0.001) for GC non-users aged 75-84 and 7.62 (95% CI 3.70-15.7, P < 0.001) for GC users aged 75-84.

Conclusions: Decline in physical function among GC users was observed in patients aged 75-84, and increasing age and GCs were mutually associated with physical dysfunction of patients in remission. Key Points • The proportion of patients who were in remission but still using glucocorticoids increased with age. • Proportions of patients in remission with HAQ-DI > 0.5 were significantly higher in the patients aged 75-84 with GCs than those without GCs but not in the patients aged 55-64 and 65-74. • Glucocorticoid use for patients in remission was more strongly associated with impaired physical function in patients aged 75-84 than in patients aged 55-74 years.

衰老和糖皮质激素使用对缓解期老年类风湿关节炎身体功能的影响:日本风湿病国家数据库的分析
目的:探讨使用糖皮质激素(GC)和不使用糖皮质激素(GC)缓解期类风湿关节炎(RA)的临床特征和身体功能。方法:从日本国家风湿病数据库(NinJa)中提取2078例年龄55 ~ 84岁缓解期(简化疾病活动指数(SDAI)≤3.3)和Steinbrocker分级为I/II期的RA患者数据,其中包括2017年至2018年冠状病毒大流行前的11036例患者。患者被分为6组:RA年龄55-64岁,65-74岁,75-84岁,伴有或不伴有GCs。主要观察指标为健康评估问卷失能指数(HAQ-DI) >.5,采用多变量logistic回归分析年龄和GC使用对HAQ-DI >.5的影响。结果:GC在缓解期患者中的使用随着年龄的增长而增加。在75-84岁伴有和不伴有GC的患者中,甲氨蝶呤和生物疾病改善抗风湿药物处方相似。75-84岁的GC用户的HAQ-DI >.5明显高于非GC用户(23.9% vs. 14.8%, P = 0.015),而65-74岁和55-64岁的用户则没有。在HAQ-DI > 0.5中,年龄与GC使用之间存在交互作用,而在HAQ-DI > 0.5中,相对于55-64岁未使用GC的患者,调整比值比(or)增加至4.72 (95% CI 2.49-8.96, P)。结论:在75-84岁的患者中,GC使用者的身体功能下降,年龄和GC的增加与缓解期患者的身体功能障碍相互相关。•患者缓解但仍在使用糖皮质激素的比例随着年龄的增长而增加。•75 ~ 84岁GCs患者HAQ-DI >.5缓解的比例显著高于无GCs患者,但55 ~ 64岁和65 ~ 74岁患者无此差异。•与55-74岁患者相比,75-84岁缓解期患者使用糖皮质激素与身体功能受损的相关性更强。
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来源期刊
Clinical Rheumatology
Clinical Rheumatology 医学-风湿病学
CiteScore
6.90
自引率
2.90%
发文量
441
审稿时长
3 months
期刊介绍: Clinical Rheumatology is an international English-language journal devoted to publishing original clinical investigation and research in the general field of rheumatology with accent on clinical aspects at postgraduate level. The journal succeeds Acta Rheumatologica Belgica, originally founded in 1945 as the official journal of the Belgian Rheumatology Society. Clinical Rheumatology aims to cover all modern trends in clinical and experimental research as well as the management and evaluation of diagnostic and treatment procedures connected with the inflammatory, immunologic, metabolic, genetic and degenerative soft and hard connective tissue diseases.
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