King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Tripoli Children Hospital, Tripoli, Libya.
Int J Rheum Dis. 2021 Aug;24(8):1080-1085. doi: 10.1111/1756-185X.14167. Epub 2021 Jun 29.
To evaluate the impact of family history of autoimmune diseases (FHADs) on the clinical characteristics and outcome of juvenile idiopathic arthritis (JIA).
We retrospectively reviewed children with JIA seen in 7 pediatric rheumatology clinics from 6 Arab countries. All included patients met the International League of Associations for Rheumatology classification criteria for JIA and had a disease duration greater than 1 year. Data were collected at the last follow-up visit and comprised clinical findings, including FHADs. Disease activity and disease damage were assessed by Juvenile Arthritis Multidimensional Assessment Report, and juvenile arthritis damage index (JADI) respectively. Disease activity was categorized as remission off treatment, remission on treatment, or active disease.
A total of 349 (224 females) JIA patients with a disease duration of 5 (interquartile range 2.9-7.5) years were included. The most frequent JIA categories were polyarticular JIA and oligoarticular JIA, followed by systemic JIA. There were 189 patients with FHADs and 160 patients without FHADs. The most frequent FHADs were diabetes mellitus (21.2%), JIA (18.5%), rheumatoid arthritis (12.7%). Among patients with FHADs, 140/189 (74.1%) achieved clinical remission, while 131/160 (81.9%) patients without FHDs had clinical remission (odds ratio [OR] = 1.2, 95% CI 0.97-1.5). Rate of consanguinity, enthesitis-related arthritis (ERA) and psoriatic arthritis were higher in patients with FHADs (OR = 0.6, 95% CI 0.4-0.9 and OR = 1.2, 95% CI 1.1-1.4). Also, articular JADI correlated significantly with presence of FHADs (OR = 1.1, 95% CI 1.0-1.1).
This study shows that autoimmune diseases cluster within families of patients with JIA with a high proportion of ERA and psoriatic arthritis. JIA patients with FHADs are likely to have more disease damage.
评估自身免疫性疾病家族史(FHADs)对幼年特发性关节炎(JIA)患者的临床特征和结局的影响。
我们回顾性分析了来自 6 个阿拉伯国家的 7 个儿科风湿病诊所的 JIA 患儿。所有纳入的患者均符合国际风湿病联盟的 JIA 分类标准,且疾病病程>1 年。数据采集于最后一次随访时,包括临床资料,包括 FHADs。疾病活动度和疾病损害分别采用幼年特发性关节炎多维评估报告和幼年特发性关节炎损害指数(JADI)评估。疾病活动度分为治疗缓解、治疗缓解和疾病活动。
共纳入 349 例(224 例女性)病程 5 年(四分位距 2.9-7.5 年)的 JIA 患儿。最常见的 JIA 类型为多关节型和少关节型,其次是全身型。189 例患者有 FHADs,160 例患者无 FHADs。最常见的 FHADs 是糖尿病(21.2%)、JIA(18.5%)、类风湿关节炎(12.7%)。在有 FHADs 的患者中,140/189 例(74.1%)达到临床缓解,而在无 FHADs 的患者中,131/160 例(81.9%)达到临床缓解(比值比[OR]为 1.2,95%CI 为 0.97-1.5)。有 FHADs 的患者中,血缘关系、附着点炎相关关节炎(ERA)和银屑病关节炎的发生率更高(OR 为 0.6,95%CI 为 0.4-0.9 和 OR 为 1.2,95%CI 为 1.1-1.4)。此外,关节 JADI 与 FHADs 的存在显著相关(OR 为 1.1,95%CI 为 1.0-1.1)。
本研究表明,JIA 患者的自身免疫性疾病存在家族聚集性,其中 ERA 和银屑病关节炎的比例较高。有 FHADs 的 JIA 患者更有可能出现疾病损害。