Abstract
BackgroundJuvenile idiopathic arthritis (JIA) is a chronic inflammatory arthritis of unknown origin which can be considered an autoimmune disease (AD). The aim of this study is to analyse the presence of two or more autoimmune diseases (polyautoimmunity) in patients suffering from JIA and to evaluate the occurrence of ADs in their families.MethodsSeventy-nine patients diagnosed with JIA aged 0–21 years, admitted to the Paediatric Rheumatology Unit, Sant’Orsola-Malpighi Hospital, Bologna were screened for ADs. Parents were asked about the presence of ADs in the living relatives of first and second degree.ResultsTwelve of 79 patients (15.2%) had at least 1 AD associated with JIA. Eight patients (10.1%) suffered from autoimmune thyroid disease (AITD), three patients had celiac disease, three patients suffered from psoriasis, one from alopecia and 1 from insulin-dependent diabetes mellitus. The average age at diagnosis was 13.2 years and the cumulative incidence of AITD was 36%. Seventy-six families were studied for a total of 438 relatives. The prevalence of ADs was 13%, greater in first-degree relatives (16.7%) than in second-degree ones (11.1%). The most common AD was AITD; there was no difference in JIA’s age of presentation between patients with positive and negative familiarity with ADs (p > 0.05).ConclusionChildren and adolescents with JIA present a high autoimmunity burden, most commonly represented by AITD. Familial autoimmunity is not negligible in patients suffering from JIA (almost 50% of patients have at least one relative with an AD) and it should always be carefully examined.
Highlights
Juvenile idiopathic arthritis (JIA) is a chronic inflammatory arthritis of unknown origin which can be considered an autoimmune disease (AD)
Children with a diagnosis of JIA according to the International League of Associations for Rheumatology Classification [10] admitted to the Pediatric Rheumatology Unit of Sant’Orsola-Malpighi Hospital in Bologna were included in the study
The study included 79 patients (51 females, median age 10.7 ± 4.7 years, range 2.8–21 years) with a diagnosis of JIA. 72,1% of patients suffered from the oligoarthritis form, 2,5% had a positive polyarticular rheumatoid factor (RF), 13,9% had a negative polyarticular factor, 5,1% had a psoriatic and a systemic onset, while 1,3% was the percentage of enthesitisrelated subset
Summary
Juvenile idiopathic arthritis (JIA) is a chronic inflammatory arthritis of unknown origin which can be considered an autoimmune disease (AD). The aim of this study is to analyse the presence of two or more autoimmune diseases (polyautoimmunity) in patients suffering from JIA and to evaluate the occurrence of ADs in their families. In children affected by JIA the occurrence of other ADs has been described in case-reports [1,2,3] or small case-series [4,5,6,7,8,9]; the majority of studies focused on patients rather than on relatives without analyzing both aspects together. The primary objective was to evaluate the polyautoimmunity in a cohort of children affected by JIA.
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