Pediatric rheumatology

Evaluation of Health Disparities in Outcomes of Patients With Juvenile Idiopathic Arthritis

J RheumatolPublished Cross-sectional study

Authors' conclusion

We found disparities in outcomes of patients with JIA related to race and ethnicity, sex, and age.

Study context

Population
Patients with juvenile idiopathic arthritis (JIA) in the Pediatric Rheumatology Care and Outcomes Improvement Network (PR-COIN) registry, a North American learning health networkanalysed
Participants
9,601 patients
Exposure
Race and ethnicity groups
Outcome
Association between race and ethnicity groups and outcomes: PGA, PtGA, active joint count, cJADAS10, arthritis-related pain intensity, morning stiffness duration
Methodological detailsregistry-based (PR-COIN)
  • Registry-based (PR-COIN)

Main finding

As reported in the abstract

Outcomes by race and ethnicity
  • Non-Hispanic Black patients had statistically higher clinical Juvenile Arthritis Disease Activity Score (cJADAS10), pain intensity, PGA and PtGA scores vs non-Hispanic White patients

Observational data: associations, not effects.

Further findings

Outcomes by current age

Current age positively and significantly associated with higher pain intensity, PGA, PtGA and cJADAS10

Outcomes by sex

Female patients had statistically higher scores vs male patients for all outcome variables assessed

Original publication

Evaluation of Health Disparities in Outcomes of Patients With Juvenile Idiopathic Arthritis. J Rheumatol. Published 15 November 2025. doi:10.3899/jrheum.2025-0313

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