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New light on uveitis in ankylosing spondylitis.
The Journal of Rheumatology
|January 1, 1991
Summary
Ankylosing spondylitis (AS) patients have a 40% uveitis prevalence. While genetics influence susceptibility, random environmental factors, not AS progression, likely trigger recurrent inflammatory eye disease.
Area of Science:
- Ophthalmology
- Rheumatology
- Genetics
Background:
- Inflammatory eye disease, specifically uveitis, is a known complication of ankylosing spondylitis (AS).
- The precise relationship between uveitis and spondyloarthropathy in AS remains poorly understood.
Purpose of the Study:
- To investigate the prevalence and potential triggers of uveitis in a large cohort of ankylosing spondylitis patients.
- To explore the genetic and environmental factors influencing the occurrence and recurrence of uveitis in AS.
Main Methods:
- A study of 1331 consecutive patients with ankylosing spondylitis was conducted.
- Prevalence of uveitis was determined, and family studies of sib pairs were performed.
- Comparisons were made between patients with and without uveitis, and potential trigger factors were analyzed in recurrent cases.
Main Results:
- Uveitis was present in 40% of AS patients (535 subjects), with nearly half experiencing over 5 attacks.
- Family studies showed a low concordance rate (43%) for uveitis among AS-concordant sib pairs.
- No significant differences were found between patients with and without uveitis, and no seasonal, infective, or other correlations were identified for recurrent disease.
Conclusions:
- Genetic background influences susceptibility to uveitis in AS.
- The pattern of uveitis suggests random environmental triggers unrelated to the underlying rheumatological disorder.
- A single case report indicated potential remission of severe uveitis after intrauterine device removal.