Phenotypic Characterization of Juvenile Idiopathic Arthritis in African American Children

The Journal of Rheumatology
|February 17, 2016
PubMed

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.
Abstract

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