Evidence map›Paper›PMID 41430695›Full record

ArticlePediatric rheumatology online journal2025

A comprehensive report of disease complications of juvenile idiopathic arthritis using a prospective cohort study.

Jacob Anderson, Kaleo Ede, Nikita Goswami, Michael Shishov, Geoffrey Thiele, Vinay Vaidya, Elisa Wershba

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Article in Pediatric rheumatology online journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Jacob AndersonDepartment of Pediatric Rheumatology, Phoenix Children's Hospital, Phoenix, AZ, USA. jake.g.anderson@hsc.utah.edu.
Kaleo EdeDepartment of Pediatric Rheumatology, Phoenix Children's Hospital, Phoenix, AZ, USA.
Nikita GoswamiDepartment of Pediatric Rheumatology, Phoenix Children's Hospital, Phoenix, AZ, USA.
Michael ShishovDepartment of Pediatric Rheumatology, Phoenix Children's Hospital, Phoenix, AZ, USA.
Geoffrey ThieleDepartment of Pediatric Rheumatology, Phoenix Children's Hospital, Phoenix, AZ, USA.
Vinay VaidyaDepartment of Pediatric Rheumatology, Phoenix Children's Hospital, Phoenix, AZ, USA.
Elisa WershbaDepartment of Pediatric Rheumatology, Phoenix Children's Hospital, Phoenix, AZ, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGiven the chronic inflammatory nature of juvenile idiopathic arthritis (JIA), disease complications may occur including chronic joint damage, ocular complications, and growth restrictions. Few studies have provided a comprehensive assessment of disease complication rates in a contemporary population of patients with JIA. The primary objective of this study was to provide a comprehensive report of disease complications in our JIA population. Secondary objectives included characterizing patients who developed complications and identifying associated risk factors.

methodsWe conducted a prospective cohort study. A standardized list of JIA disease complications was created by consensus among rheumatologists and included in the electronic medical record. A total of 432 patients diagnosed with JIA for more than one year were evaluated at our rheumatology clinic between January 2023 and February 2024 and were assessed for the development of disease complications. Univariate analysis was used to test for associations between the presence of complications and potential risk factors such as sex, age of disease onset, diagnosis duration, serology positivity, and treatment history.

resultsOf the 432 patients, 146 (33.8%) were identified to have at least one disease complication. Joint complications occurred in 73 patients (16.9%), and uveitis was identified in 57 patients (13.2%), with 14 (25%) of those experiencing secondary ocular complications. Growth failure was observed in 4% of patients, with short stature resulting in 1%. Younger age at disease onset and longer time to initiation of biologic therapy were associated with an increased risk of developing complications. Additionally, delayed initial rheumatology evaluation and delayed initiation of biologic therapy were both associated with a progressively increasing risk of joint complications.

conclusionDespite therapeutic advances in the treatment of JIA, a substantial proportion of patients continue to develop disease complications. Approximately one-third of patients in our cohort experienced at least one disease complication. Delayed initiation of biologic therapy was associated with higher complication rates, highlighting the importance of early therapeutic intervention to reduce the burden of disease complications.

Indexed as

Arthritis, JuvenileUveitisAdolescentChildChild, PreschoolFemaleGrowth DisordersHumansMaleProspective StudiesRisk FactorsBiologicsDisease complicationsGrowth failureJoint damageJuvenile idiopathic arthritisUveitis

Identifiers

PMID41430695
PMCPMC12751286

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