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Published on: March 1, 2024
Occurrence and Risk Factors of Uveitis in Juvenile Psoriatic Arthritis: Data From a Population-based Nationwide Study
Karoline Baquet-Walscheid1, Kai Rothaus2, Martina Niewerth3
1K. Baquet-Walscheid, MD, A. Heiligenhaus, MD, Department of Ophthalmology at St. Franziskus Hospital, Muenster, and University of Duisburg-Essen, Faculty of Medicine, Essen; karoline.walscheid@uveitis-zentrum.de.
Insights
Juvenile psoriatic arthritis (JPsA) affects 6.6% of patients with uveitis, particularly females and those with early disease onset. Early-onset JPsA increases ocular involvement risk, highlighting distinct clinical differences.
Area of Science:
- Pediatric Rheumatology
- Ophthalmology
- Immunology
Background:
- Uveitis data in juvenile psoriatic arthritis (JPsA), a subset of juvenile idiopathic arthritis (JIA), are limited.
- Understanding JPsA-associated uveitis (JPsA-U) prevalence and risk factors is crucial for early detection and management.
Purpose of the Study:
- To determine the prevalence of uveitis in a cohort of patients with JPsA.
- To identify clinical and demographic risk factors associated with the development of uveitis in JPsA patients.
Main Methods:
- Cross-sectional analysis of data from the German National Pediatric Rheumatological Database (2002-2014).
- Characterization of JPsA-U patients and assessment of risk factors using multivariable analysis.
- Subgroup analysis focused on patients with early arthritis onset (within 1 year).
Main Results:
- Uveitis occurred in 6.6% of 1862 JPsA patients.
- JPsA-U patients were more frequently female, antinuclear antibody (ANA)-positive, younger at onset, and treated with DMARDs.
- Early-onset JPsA (<5 years) was associated with higher ANA positivity, uveitis incidence, and DMARD use, but less skin disease.
Conclusions:
- Characteristics of JPsA-U resemble those in other JIA categories like oligoarticular JIA.
- Children with early-onset JPsA face a significantly higher risk of ocular complications.
- Distinct clinical differences exist between early-onset and late-onset JPsA patients.
Objective:
Data on uveitis in juvenile psoriatic arthritis (JPsA), a category of juvenile idiopathic arthritis (JIA), are scarce. We describe prevalence and risk factors for JPsA-associated uveitis (JPsA-U).
Methods:
Cross-sectional data from the German National Pediatric Rheumatological Database (2002-2014) were used to characterize JPsA-U and assess risk factors for the development of uveitis.
Results:
Uveitis developed in 6.6% of 1862 patients with JPsA. Patients with JPsA-U were more frequently female (73.0 vs 62.9%, P = 0.03), antinuclear antibody (ANA) positive (60.3 vs 37.0%, P < 0.001), younger at JPsA onset (5.3 ± 4.1 vs 9.3 ± 4.4 yrs, P < 0.001), and treated with disease-modifying antirheumatic drugs (DMARDs) significantly more frequently compared with JPsA patients without uveitis. On a multivariable analysis of a subgroup of 655 patients enrolled in the study ≤ 1 year after arthritis onset, mean clinical Juvenile Arthritis Disease Activity Score for 10 joints during study documentation was significantly associated with uveitis development. Children with early onset of JPsA (aged < 5 yrs vs ≥ 5 yrs) were significantly more frequently ANA positive (48.4% vs 35.7%, P < 0.001), affected by uveitis (17.3% vs 3.8%, P < 0.001), and treated with DMARDs (52.9% vs 43.8%, P < 0.001), but less often affected by skin disease (55.3% vs 61.0%, P = 0.03).
Conclusion:
The characteristics of patients with JPsA developing uveitis are similar to those of patients with uveitis in other JIA categories, such as oligoarticular JIA. Children with early-onset JPsA are at a higher risk for ocular involvement. Our data support the notion of a major clinical difference between those patients with early vs late onset of JPsA.
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