From: Is juvenile rheumatoid arthritis/juvenile idiopathic arthritis different from rheumatoid arthritis?
Feature | RA | JRA/JIA |
---|---|---|
Classification criteria | Single disease with different manifestations | Phenotypically and genetically distinct subtypes |
Gender | Females > males | Females > males except in systemic arthritis |
Age of onset | Puberty plus; peak 4th to 5th decade | Polyarticular: throughout childhood; peak 1-3 years of age |
 |  | Pauciarticular: early childhood; peak 1-2 years of age |
 |  | Systemic: throughout childhood; no peak |
Extended multiplex families | Present | Very rare |
Family history of other autoimmune disorders | Present | Present |
Typical ocular involvement | Keratoconjunctivitis sicca | Chronic anterior uveitis |
Prevalence | 10/1000 | 0.86/1000 |
Ethnic distribution | Reported in all populations | EOPA is rare in non-Caucasians |
HLA association | HLA DRB1*0401, 0404, 0101 in Caucasians | EOPA: HLA-A2, -DR5, -DR8, -DPB1*0201. (HLA-DR4 is protective) |
 |  | Late pauciarticular: HLA-B27 |
 |  | Polyarticular: HLA-DR1, -DR4 |
Shared epitope | Defined; amino acid positions 67-74 of third hypervariable region | Not described |
Growth/developmental issues | Rare | Common |
Pathophysiology | Th1-mediated disease | Th1-mediated disease (Pauciarticular: Also Th2-mediated) |
Autoantibodies | IgM RF common | IgM RF rare |
Natural history | Majority have long-term disability | Fewer than half have long-term disability |