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Phenotypic Characterization of Juvenile Idiopathic Arthritis in African American Children
Insights
African American children with juvenile idiopathic arthritis (JIA) more often present with rheumatoid factor-positive polyarthritis and are older at disease onset compared to non-Hispanic white children.
Area of Science:
- Pediatric Rheumatology
- Immunology
- Genetics
Background:
- Juvenile idiopathic arthritis (JIA) is a heterogeneous autoimmune disease affecting children.
- Previous research indicates potential differences in JIA presentation between racial groups.
- African American (AA) children may exhibit distinct phenotypic features compared to non-Hispanic White (NHW) children.
Purpose of the Study:
- To investigate and compare the phenotypic characteristics of JIA at presentation between AA and NHW children.
- To validate observed differences in a separate JIA cohort from the southeastern United States.
Main Methods:
- Analysis of phenotypic data from AA and NHW children with JIA within the Childhood Arthritis and Rheumatology Research Alliance (CARRA) Registry.
- Replication of findings using a JIA cohort from Emory University.
- Statistical comparison using chi-square, Fisher's exact, and Wilcoxon signed-rank tests.
Main Results:
- AA children were more frequently diagnosed with rheumatoid factor (RF)-positive polyarthritis in both cohorts (CARRA: 13.4% vs 4.7%; Emory: 26.8% vs 6.1%).
- AA children showed higher rates of positive RF and cyclic citrullinated peptide (CCP) antibodies but lower rates of oligoarticular or antinuclear antibody (ANA)-positive JIA.
- AA children were significantly older at disease onset (CARRA Registry median age 8.5 vs 5.0 years).
Conclusions:
- The phenotype of JIA differs between AA and NHW children.
- AA children with JIA are more prone to RF/CCP-positive polyarthritis and present at an older age.
- Early-onset, oligoarticular, or ANA-positive JIA is less common in AA children compared to NHW children.
Objective:
Juvenile idiopathic arthritis (JIA) affects children of all races. Prior studies suggest that phenotypic features of JIA in African American (AA) children differ from those of non-Hispanic white (NHW) children. We evaluated the phenotypic differences at presentation between AA and NHW children enrolled in the Childhood Arthritis and Rheumatology Research Alliance (CARRA) Registry, and replicated the findings in a JIA cohort from a large center in the southeastern United States.
Methods:
Children with JIA enrolled in the multicenter CARRA Registry and from Emory University formed the study and replication cohorts. Phenotypic data on non-Hispanic AA children were compared with NHW children with JIA using the chi-square test, Fisher's exact test, and the Wilcoxon signed-rank test.
Results:
In all, 4177 NHW and 292 AA JIA cases from the CARRA Registry and 212 NHW and 71 AA cases from Emory were analyzed. AA subjects more often had rheumatoid factor (RF)-positive polyarthritis in both the CARRA (13.4% vs 4.7%, p = 5.3 × 10(-7)) and the Emory (26.8% vs 6.1%, p = 1.1 × 10(-5)) cohorts. AA children had positive tests for RF and cyclic citrullinated peptide antibodies (CCP) more frequently, but oligoarticular or early onset antinuclear antibody (ANA)-positive JIA less frequently in both cohorts. AA children were older at onset in both cohorts and this difference persisted after excluding RF-positive polyarthritis in the CARRA Registry (median age 8.5 vs 5.0 yrs, p = 1.4 × 10(-8)).
Conclusion:
Compared with NHW children, AA children with JIA are more likely to have RF/CCP-positive polyarthritis, are older at disease onset, and less likely to have oligoarticular or ANA-positive, early-onset JIA, suggesting that the JIA phenotype is different in AA children.
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