Abstract

BackgroundJuvenile idiopathic arthritis constitutes a significant cause of disability and quality of life impairment in pediatric and adult patients. The aim of this study was to ascertain clinical remission (CR) and subsequent relapse in juvenile idiopathic arthritis (JIA) patients, according to therapeutic approach and JIA subtype. Evidence in literature regarding its predictors is scarce.MethodsWe conducted an observational, ambispective study. Patients diagnosed of JIA, treated with synthetic and/or biologic disease modifying antirheumatic drugs (DMARD) were included and followed-up to December 31st, 2015. Primary outcome was clinical remission defined by Wallace criteria, both on and off medication. In order to ascertain CR according to therapeutic approach, DMARD treatments were divided in four groups: 1) synthetic DMARD (sDMARD) alone, 2) sDMARD combined with another sDMARD, 3) sDMARD combined with biologic DMARD (bDMARD), and 4) bDMARD alone.ResultsA total of 206 patients who received DMARD treatment were included. At the time the follow-up was completed, 70% of the patients in the cohort had attained CR at least once (144 out of 206), and 29% were in clinical remission off medication (59 out of 206).According to treatment group, CR was more frequently observed in patients treated with synthetic DMARD alone (53%). Within this group, CR was associated with female sex, oligoarticular persistent subtypes, ANA positivity, Methotrexate treatment and absence of HLA B27, comorbidities and DMARD toxicity. 124 DMARD treatments (62%) were withdrawn, 64% of which relapsed. Lower relapse rates were observed in those patients with persistent oligoarticular JIA (93%) when DMARD dose was tapered before withdrawal (77%).ConclusionsMore than two thirds of JIA patients attained CR along the 9 years of follow-up, and nearly one third achieved CR off medication. Females with early JIA onset, lower active joint count and ANA positivity were the ones achieving and sustaining remission more frequently, especially when receiving synthetic DMARD alone and in the absence of HLA B27, comorbidities or previous DMARD toxicity.

Highlights

  • Juvenile idiopathic arthritis constitutes a significant cause of disability and quality of life impairment in pediatric and adult patients

  • A retrospective cohort was created on January 1st, 2012, in which patients diagnosed of juvenile idiopathic arthritis (JIA), treated with Disease Modifying Antirheumatic Drugs (DMARD), and followed-up to December 31st, 2013, were included

  • A total of 264 patients meeting the ILAR diagnostic criteria for JIA were included, of which 254 had received DMARD. 206 patients were included in the retrospective study, which received 764

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Summary

Introduction

Juvenile idiopathic arthritis constitutes a significant cause of disability and quality of life impairment in pediatric and adult patients. Juvenile idiopathic arthritis is the most common chronic rheumatic disease in childhood This term comprises an heterogenous group of arthritis of unknown aetiology, each of which has differential genetics, etiopathogenesis, onset age and disease outcomes [1, 2]. It constitutes a significant cause of disability and quality of life impairment in JIA pediatric and adult patients [3,4,5]. A notable proportion of patients relapse, either while still on medication or after its withdrawal [10,11,12]

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