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Author Notes:

Author for correspondence: Tel.: +1 404 778 2400, Fax: +1 404 727 3757, sangele@emory.edu

Subject:

Research Funding:

Research reported in this publication was supported by the National Eye Institute of the NIH under Award Number K23 EY021760 to ST Angeles-Han.

S Yeh received research support via an Unrestricted Grant from Research to Prevent Blindness (Emory Eye Center) and the Knights Templar Foundation.

Keywords:

  • juvenile arthritis
  • juvenile idiopathic arthritis-associated uveitis
  • ocular disease
  • pediatric rheumatology
  • risk
  • uveitis

Updates on the risk markers and outcomes of severe juvenile idiopathic arthritis-associated uveitis

Tools:

Journal Title:

International Journal of Clinical Rheumatology

Volume:

Volume 8, Number 1

Publisher:

, Pages 109-121

Type of Work:

Article | Post-print: After Peer Review

Abstract:

Uveitis is the most common extra-articular manifestation of juvenile idiopathic arthritis, which is the most common systemic cause of uveitis in children. Known risk factors for uveitis include antinuclear antibody seropositivity, young age of arthritis onset, specific juvenile idiopathic arthritis subtype and short duration of disease. Risk markers for severe ocular disease include gender, age and complications at initial visit. Due to the risk for vision-compromising sequelae such as cataracts, band keratopathy, glaucoma, vision loss and blindness, an understanding of the risk factors for uveitis development and severe ocular disease is crucial to help prevent serious visual disability and complications. This paper reviews the pathogenesis of uveitis, known risk factors for uveitis development and severe visual outcome, and addresses the need for additional biomarkers of uveitis risk, prognosis and remission.

Copyright information:

© 2013 Future Medicine Ltd

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