Clinical insights into heterogeneity of rheumatoid factor negative polyarticular juvenile idiopathic arthritis across the world.

IF 2.8 3区 医学 Q1 PEDIATRICS
Roberta Naddei, Marco Burrone, Francesca Ridella, Yosef Uziel, Maria Trachana, Pavla Dolezalova, Ingrida Rumba-Rozenfelde, Nicolino Ruperto, Angelo Ravelli, Alessandro Consolaro
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Abstract

Background: To our knowledge, limited information is available about the differences in the characteristics of rheumatoid factor (RF)-negative polyarticular juvenile idiopathic arthritis (JIA) throughout the world. This study was aimed to compare the demographic and clinical features of patients with RF-negative polyarthritis across the world.

Methods: Patients were part of a multinational sample included in a study aimed to investigate the prevalence of disease categories, treatment regimens, and disease status in patients from different geographical areas (EPOCA Study). All patients underwent a retrospective assessment, based on the review of clinical chart, and a cross-sectional evaluation, which included assessment of physician- and parent-reported outcomes and collection of ongoing medications.

Results: Among the 9081 patients enrolled in the EPOCA study, 2141 patients (23.6%) with RF-negative polyarthritis were included in the present analysis. The prevalence of RF-negative polyarthritis was highest in North America and lowest in Southeast Asia (12.7%). The age at disease onset was lower in Northern and Southern Europe, where the highest prevalence of uveitis was found. Uveitis was rare in Southeast Asia, Africa & Middle East and Latin America. Patients from Eastern Europe, Latin America and Africa and Middle East presented with the highest prevalence of active joints at the visit. The combination of early onset, ANA positivity, and uveitis was observed mainly in Southern Europe (39%).

Conclusions: Our results confirm the wide heterogeneity of the clinical presentation and outcome of children with RF-negative polyarticular JIA throughout the world. In particular, relevant differences in the onset age were observed across geographic areas. The group of children with early onset polyarthritis, ANA positivity, and risk of uveitis is remarkably frequent in Southern Europe.

世界各地类风湿因子阴性多关节幼年特发性关节炎异质性的临床见解。
背景:据我们所知,关于世界各地类风湿因子(RF)阴性多关节幼年特发性关节炎(JIA)特征差异的信息有限。本研究旨在比较世界各地rf阴性多发性关节炎患者的人口统计学和临床特征。方法:患者是多国样本的一部分,该研究旨在调查来自不同地理区域的患者的疾病类别、治疗方案和疾病状态的流行情况(EPOCA研究)。所有患者都进行了回顾性评估,基于对临床图表的回顾,并进行了横断面评估,包括评估医生和家长报告的结果以及收集正在使用的药物。结果:在纳入EPOCA研究的9081例患者中,2141例(23.6%)rf阴性多发性关节炎患者被纳入本分析。rf阴性多发性关节炎的患病率在北美最高,在东南亚最低(12.7%)。在葡萄膜炎发病率最高的北欧和南欧,发病年龄较低。葡萄膜炎在东南亚、非洲、中东和拉丁美洲很少见。来自东欧、拉丁美洲、非洲和中东的患者在访问中表现出关节活动的最高患病率。早发、ANA阳性和葡萄膜炎的合并主要见于南欧(39%)。结论:我们的研究结果证实了世界范围内rf阴性多关节性JIA患儿的临床表现和预后的广泛异质性。特别是,不同地理区域的发病年龄存在相关差异。早发性多关节炎、ANA阳性和葡萄膜炎风险的儿童群体在南欧非常常见。
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来源期刊
Pediatric Rheumatology
Pediatric Rheumatology PEDIATRICS-RHEUMATOLOGY
CiteScore
4.10
自引率
8.00%
发文量
95
审稿时长
>12 weeks
期刊介绍: Pediatric Rheumatology is an open access, peer-reviewed, online journal encompassing all aspects of clinical and basic research related to pediatric rheumatology and allied subjects. The journal’s scope of diseases and syndromes include musculoskeletal pain syndromes, rheumatic fever and post-streptococcal syndromes, juvenile idiopathic arthritis, systemic lupus erythematosus, juvenile dermatomyositis, local and systemic scleroderma, Kawasaki disease, Henoch-Schonlein purpura and other vasculitides, sarcoidosis, inherited musculoskeletal syndromes, autoinflammatory syndromes, and others.
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