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Juvenile idiopathic arthritis profile in Turkish children
Mustafa Yilmaz1, Seval G Kendirli, Derya U Altintas
1Division of Pediatric Allergy and Immunology, Cukurova University Faculty of Medicine, Adana, Turkey. yilmazm@cu.edu.tr
Insights
Juvenile idiopathic arthritis (JIA) in Turkish children presents differently than in Western populations, with a higher incidence of polyarticular JIA and a greater prevalence in boys. This study highlights distinct clinical and laboratory features in this demographic.
Area of Science:
- Pediatric Rheumatology
- Clinical Immunology
- Genetics and Epidemiology
Background:
- Juvenile idiopathic arthritis (JIA) is a diverse autoimmune condition with varying manifestations across different global populations.
- Previous studies suggest geographical differences in JIA presentation, necessitating localized research.
- Understanding these variations is crucial for accurate diagnosis and tailored treatment strategies.
Purpose of the Study:
- To investigate the specific clinical and laboratory characteristics of JIA in a cohort of Turkish children.
- To compare the findings in Turkish children with those reported in Western populations.
- To identify potential genetic or environmental factors influencing JIA expression in Turkey.
Main Methods:
- A retrospective analysis of 196 pediatric patients diagnosed with JIA according to International League of Associations for Rheumatology (ILAR) criteria.
- Collection of demographic data, disease onset, diagnosis age, and follow-up duration.
- Laboratory investigations included antinuclear antibody (ANA), rheumatoid factor (RF), and human leukocyte antigen B-27 (HLA-B27).
Main Results:
- Polyarticular JIA was the most common subtype (37.2%), followed by oligoarthritis (34.2%).
- The study observed a higher prevalence in boys (102 boys vs. 94 girls) and a lower rate of antinuclear antibody (ANA) positivity (14.2%).
- Uveitis was less common, and three patients (1.4%) developed amyloidosis.
Conclusions:
- Turkish children exhibit distinct JIA features compared to Western cohorts, including a higher frequency of polyarticular JIA and male predominance.
- Lower rates of ANA positivity and uveitis were noted in this Turkish cohort.
- Further research is warranted to elucidate the impact of genetic and environmental factors on JIA presentation in diverse populations.
Background:
Juvenile idiopathic arthritis (JIA) is a heterogeneous group of disorders. Publications from different countries point to differences in the disease manifestation of JIA among different populations. The aim of the present paper was to evaluate the clinical and laboratory features of JIA in Turkish children.
Methods:
A total of 196 JIA patients who fulfilled International League of Associations for Rheumatology (ILAR) diagnostic criteria were included in this retrospective study. The data collected were age, gender, age at disease onset and at diagnosis, and follow-up duration. Antinuclear antibody (ANA), rheumatoid factor (RF), and human leukocyte antigen B-27 were evaluated for each patient.
Results:
There were 102 boys and 94 girls with a mean duration of disease of 4.1 years. The mean age at the first visit was 8.8 years, and the mean age at onset of disease was 6.8 years (range, 8 months-15 years). Polyarticular JIA was the most frequent onset type (37.2%). Other subtypes included oligoarthritis (34.2%), systemic arthritis (15.3%), psoriatic arthritis (1%), enthesitis-related arthritis (9.7%), and other arthritis (2.2%). ANA was positive in 28 patients (14.2%). Chronic uveitis occurred in two patients with oligoarthritis; and two patients with enthesitis-related arthritis had acute uveitis. Three patients (1.4%) developed amyloidosis.
Conclusion:
Compared to reports from Western countries, remarkably different features of JIA were found in Turkish children, which included higher frequency of polyarticular JIA, higher prevalence among boys, lower rate of ANA positivity and uveitis. Further studies are required to understand how genetic and environmental differences affect JIA expression.
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