Department of Pediatric Respiratory Medicine, Immunology and Critical Care Medicine, Children's university hospital Charité, Augustenburger Platz 1, 13353, Berlin, Germany.
Institute of Biometry and Clinical Epidemiology and Berlin Institute of Health, Charité - Universitätsmedizin, Berlin, Germany.
Pediatr Rheumatol Online J. 2021 Mar 22;19(1):41. doi: 10.1186/s12969-021-00522-4.
Oligoarticular juvenile idiopathic arthritis (oligoJIA) is the most commonly diagnosed category of chronic arthritis in children. Nevertheless, there are no evidence- based guidelines for its treatment, in particular for the use of methotrexate (MTX). The primary objective of this analysis is to evaluate the outcomes in patients with persistent oligoJIA compared to those with extended oligoJIA and rheumatoid factor (RF) negative polyarthritis treated with methotrexate.
Patients with persistent or extended oligoJIA or RF negative PA recorded in the Biologics in Pediatric Rheumatology Registry (BiKeR), receiving methotrexate for the first time were included in the analyses. Efficacy was determined using the Juvenile Arthritis Disease Activity Score 10 (JADAS 10). Safety assessment included the documentation of adverse and serious adverse events.
From 2005 through 2011, 1056 patients were included: 370 patients with persistent oligoJIA, 221 patients with extended oligoJIA and 467 patients with RF negative PA. Therapeutic efficacy was observed following the start of methotrexate. Over a period of 24 months JADAS-minimal disease activity (JADAS ≤2) was reached in 44% of patients with persistent oligoJIA, 38% with extended oligoJIA, 46% with RF negative PA, JADAS-remission defined as JADAS ≤1 was reached in 33% of patients with persistent oligoJIA, 29% with extended oligoJIA and 35% (RF negative PA). Patients with extended oligoJIA achieved JADAS remission significantly later and received additional biologic disease-modifying drugs significantly more often than patients with persistent oligoJIA or RF negative PA (p < 0.001). Tolerability was comparable. New onset uveitis occurred in 0.3 to 2.2 per 100 patient years.
Patients with persistent oligoJIA taking methotrexate are at least as likely to enter remission as patients with extended oligo JIA or polyarticular JIA. Patients with extended oligoJIA achieved JADAS remission significantly later. Within 2 years, almost half of the patients with persistent oligoJIA achieved JADAS-minimal disease activity.
寡关节型幼年特发性关节炎(oligoJIA)是儿童中最常见的慢性关节炎类型。然而,目前尚无针对该疾病的循证治疗指南,尤其是在使用甲氨蝶呤(MTX)方面。本分析的主要目的是评估持续性寡关节型 JIA 患者与扩展性寡关节型 JIA 患者和 RF 阴性多关节炎患者相比,接受 MTX 治疗后的结局。
本研究纳入了在儿科风湿病生物制剂注册研究(Biologics in Pediatric Rheumatology Registry,BiKeR)中首次接受 MTX 治疗的持续性或扩展性寡关节型 JIA 或 RF 阴性多关节炎患者。采用 JADAS10 评估疗效。安全性评估包括不良事件和严重不良事件的记录。
2005 年至 2011 年期间,共纳入 1056 例患者:370 例持续性寡关节型 JIA 患者、221 例扩展性寡关节型 JIA 患者和 467 例 RF 阴性多关节炎患者。在开始 MTX 治疗后观察到了治疗效果。在 24 个月的治疗期间,44%的持续性寡关节型 JIA 患者、38%的扩展性寡关节型 JIA 患者和 46%的 RF 阴性多关节炎患者达到了 JADAS 最小疾病活动度(JADAS≤2),33%的持续性寡关节型 JIA 患者、29%的扩展性寡关节型 JIA 患者和 35%的 RF 阴性多关节炎患者达到了 JADAS 缓解(定义为 JADAS≤1)。与持续性寡关节型 JIA 或 RF 阴性多关节炎患者相比,扩展性寡关节型 JIA 患者达到 JADAS 缓解的时间明显较晚,并且更常需要接受额外的生物 DMARD 治疗(p<0.001)。两组的耐受性相当。新发生的葡萄膜炎发生率为 0.3-2.2/100 患者年。
接受 MTX 治疗的持续性寡关节型 JIA 患者进入缓解状态的可能性至少与扩展性寡关节型 JIA 或多关节炎型 JIA 患者相当。扩展性寡关节型 JIA 患者达到 JADAS 缓解的时间明显较晚。在 2 年内,近一半的持续性寡关节型 JIA 患者达到了 JADAS 最小疾病活动度。