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Characteristics of JIA-associated uveitis at the age of transition
Raymond Anna1,2, A Combier3, S Hecquet3
1Rheumatology Department, Cochin Hospital, Université Paris Cité, APHP, Paris, France. anna.raymond@aphp.fr.
Insights
Juvenile idiopathic arthritis (JIA) with uveitis poses significant risks during the transition to adult care, with many patients experiencing active inflammation and vision complications. Continuous ophthalmologic monitoring and multidisciplinary collaboration are crucial for managing JIA-associated uveitis.
Area of Science:
- Pediatric Rheumatology
- Ophthalmology
- Immunology
Background:
- Juvenile idiopathic arthritis (JIA) is a prevalent childhood rheumatic disease.
- Uveitis is the most common JIA complication, leading to significant visual impairment.
- Transitioning from pediatric to adult care is a critical period for JIA patients with uveitis.
Purpose of the Study:
- To describe ophthalmologic and rheumatologic disease characteristics in JIA patients during their transition to adult care.
- To identify key challenges and complications associated with JIA-uveitis at this transition point.
Main Methods:
- Retrospective cohort study of JIA patients with uveitis transitioning to adult care (2016-2024).
- Data collected from electronic medical records, including clinical, ophthalmologic, and treatment details.
- Descriptive statistics used; comparative analyses were exploratory.
Main Results:
- 46 patients included; predominantly female (80%) with oligoarticular JIA (59%).
- High prevalence of chronic uveitis (83%) and ocular complications (46%), including cataract and glaucoma.
- Over half experienced multiple flares; 53% required biologic disease-modifying antirheumatic drugs (DMARDs).
Conclusions:
- JIA-associated uveitis presents a substantial burden at transition, marked by complications and persistent activity.
- Structured, continuous ophthalmologic follow-up is essential for all JIA subtypes.
- Multidisciplinary collaboration is vital to prevent long-term ocular damage and preserve vision.
Background:
Juvenile idiopathic arthritis (JIA) is the most common rheumatic disease in children. Uveitis is the most frequent extra-articular manifestation of JIA and a major cause of visual morbidity. Despite advances in immunomodulatory therapy, many patients reach adulthood with active ocular inflammation or vision-threatening complications. The transition from pediatric to adult care represents a vulnerable period. The primary objective of our study is to describe ophthalmologic and rheumatologic disease characteristics at the time of transition from pediatric to adult care.
Methods:
We conducted a retrospective cohort study of patients with JIA and past or present uveitis who transitioned to adult rheumatology at Cochin Hospital between 2016 and 2024. Clinical, ophthalmologic, and therapeutic data were collected from electronic medical records. Descriptive statistics were performed. Comparative analyses were exploratory and intended to describe differences between subgroups rather than to test predefined hypotheses.
Results:
A total of 46 patients were included. Median age at JIA diagnosis was 7.5 years [IQR 2.0-16.0] and median age at first uveitis was 6.0 years [IQR 3.0-12.2]. Median follow-up after transition was 2.44 years [IQR 1.17-3.94]. Most patients were female (80%, n = 37) and had oligoarticular JIA (59%, n = 27). Chronic uveitis predominated (83%, n = 38). Ocular complications occurred in 46% (n = 17), including cataract (24%, n = 11), glaucoma (20%, n = 9), and keratitis (7%, n = 3). Over half (57%, n = 13/23) experienced ≥ 5 flares since diagnosis. Biologic DMARDs were prescribed in 53% (n = 23/43), predominantly anti-TNF agents.
Conclusion:
This study highlights the substantial burden of JIA-associated uveitis at the time of transition to adult care, characterized by frequent complications, persistent disease activity, and a high need for biologic therapy. Our findings emphasize the necessity of structured and continuous ophthalmologic follow-up across all JIA subtypes, alongside close multidisciplinary collaboration, to prevent long-term ocular damage and preserve visual function.
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