Evidence map›Paper›PMID 42184063›Full record

ArticleInternational ophthalmology2026

Clinical characteristics and factors associated with uveitis in juvenile idiopathic arthritis: a long-term single-center experience.

Doğacan Sarısoy, Fatma Aydın, Pınar Özge Avar Aydın, Fatime Nilüfer Yalçındağ, Zeynep Birsin Özçakar

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Article in International ophthalmology, 2026. 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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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Doğacan SarısoyDepartment of Pediatrics, Division of Pediatric Rheumatology, Ankara University School of Medicine, Ankara, Turkey.ORCID http://orcid.org/0000-0002-2583-8948
Fatma AydınDepartment of Pediatrics, Division of Pediatric Rheumatology, Ankara University School of Medicine, Ankara, Turkey. fatma4326@yahoo.com.ORCID http://orcid.org/0000-0003-0306-7473
Pınar Özge Avar AydınDepartment of Pediatrics, Division of Pediatric Rheumatology, Ankara University School of Medicine, Ankara, Turkey.ORCID http://orcid.org/0000-0002-7469-109X
Fatime Nilüfer YalçındağDepartment of Ophtalmology, Ankara University School of Medicine, Ankara, Turkey.ORCID http://orcid.org/0000-0002-8963-5146
Zeynep Birsin ÖzçakarDepartment of Pediatrics, Division of Pediatric Rheumatology, Ankara University School of Medicine, Ankara, Turkey.ORCID http://orcid.org/0000-0002-6376-9189

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeJuvenile Idiopathic Arthritis uveitis (JIA-U) can progress without obvious clinical signs and cause permanent damage if left untreated, therefore early detection through regular screening is crucial for managing the disease. This study aimed to evaluate the prevalence of uveitis and factors associated with uveitis in Juvenile Idiopathic Arthritis (JIA) patients.

methodsThe medical records of patients with a diagnosis of non-systemic JIA who were under the care of the Department of Paediatric Rheumatology at Ankara University between June 2010 and June 2024 were reviewed retrospectively. The demographic, clinical and laboratory characteristics of the patients were recorded and compared between those with and without uveitis.

results144 patients (92 girls, 63.9%; 83 oligoarticular JIA, 57.6%) were included in the study. Uveitis was detected in 26 patients (18.1%). 12 patients (46.2%) with JIA-U experienced complications and 3 of these patients had complications at the time of JIA-U diagnosis. The group who experienced JIA-U was characterised with female sex (p = 0.048), anti-nuclear antibody (ANA) positivity (p = 0.039), younger age at the time of JIA diagnosis (p = 0.014), and more frequent articular flare-ups (p = 0.014). No significant difference was found between the groups when comparing JIA subtypes and affected joints (p > 0.05).

conclusionUveitis may present with an insidious clinical course in patients with JIA. Particularly, early onset of the disease, female gender, positive ANA status, and articular relapses should be considered warning signs for uveitis.

Indexed as

Arthritis, JuvenileUveitisAdolescentChildChild, PreschoolFemaleFollow-Up StudiesHumansMalePrevalenceRetrospective StudiesRisk FactorsTime FactorsTurkeyInflammatory uveitisJuvenile idiopathic arthritisPediatric rheumatologyUveitis

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.