5-Minute Clinical Consult

Arthritis, Juvenile Idiopathic

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Basics

Description

  • Most common chronic rheumatic illness in children and a significant cause of short- and long-term disability
  • General characteristics:
    • Age of onset <16 years
    • Signs of arthritis: Joint swelling, limitation of motion, pain, heat, or tenderness
    • >6 weeks of symptoms
  • 7 subtypes exist, according to the International League of Associations for Rheumatology, determined by clinical characteristics seen in first 6 months of illness (1):
    • Systemic (Still disease): 10–20%; usually characterized by febrile onset and evanescent rash with multiple physical and laboratory abnormalities
    • Polyarticular rheumatoid factor (RF) (+): 5–10%; multiple (≥5) joint involvement; large and small joints affected. RF positive 2× on tests at least 3 months apart.
    • Polyarticular RhF (–): 30%; ≥5 joint involvement, large and small joints affected; RF negative
    • Oligoarticular: 40–50%; involvement of ≤4 joints, usually larger joints, especially of lower extremities; risk for chronic uveitis in young girls and axial skeletal involvement in older boys
    • Psoriatic arthritis: 2–15%; arthritis with psoriasis or arthritis with at least 2 of following: Dactylitis, nail pitting or onycholysis, psoriasis in 1st-degree relative
    • Enthesitis arthritis: 1–7%; includes ankylosing spondylitis and inflammatory bowel disease–related arthritis. Peripheral and axial involvement.
    • Undifferentiated arthritis: Arthritis that does not fulfill above categories or fills ≥2 categories
  • System(s) affected: Hematologic/Lymphatic/Immunologic; Musculoskeletal
  • Synonym(s): Juvenile chronic arthritis; Juvenile arthritis; Juvenile rheumatoid arthritis (JRA); Still disease

Epidemiology

  • Systemic: Girls = Boys; onset is throughout childhood (2)
  • Polyarticular RF (+): Girls > Boys 3:1; age of onset late childhood or adolescence (2)
  • Polyarticular (–): Girls > Boys 3:1; age of onset early peak 2–4 years and late peak 6–12 years
  • Oligoarticular: Girls > Boys 5:1; age of onset peak 2–4 years (2)
  • Psoriatic: Girls > Boys 1:0.95; age of onset late childhood or adolescence (2)
  • Enthesitis: Girls < Boys 1:7; age of onset early peak 2–4 years and late peak 6–12 years (2)
  • Affected patients have and increased risk of developing cancer, although short-term risk is found to be low (3,4).

Incidence
1–22 per 100,000 children <16 years per year

Prevalence
8–150 per 100,000 children <16 years

Risk Factors


Genetics
  • Certain human leukocyte antigen (HLA) class I and II alleles
  • HLA-A2 in early-onset oligoarthritis in girls
  • HLA-DRB1*11 confers increased risk of systemic and oligo-JIA.
  • HLA-B27 risk of enthesitis-related arthritis
  • HLA-DR4 associated with RF (+) polyarticular disease

General Prevention

No known preventive measures

Etiology

Multifactorial, including:

  • Immunodysregulation
  • Genetic predisposition
  • Environmental triggers, possibly infectious:
    • Rubella or parvovirus B19 (5)
    • Heat shock proteins (5)
  • Immunoglobulin or complement deficiency

Commonly Associated Conditions

Other autoimmune disorders, chronic anterior uveitis (iridocyclitis), nutritional impairment, growth disturbances (5)

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