Abstract | OBJECTIVE: DESIGN: Fifty-three patients with the diagnosis of pars planitis underwent clinical record review or telephone interview for follow-up or both; 32 of these underwent phlebotomy for analysis of HLA class II alleles. MAIN OUTCOME MEASURES: RESULTS: With a mean follow-up of 2 years, approximately 90% of patients maintained a visual acuity better than 20/40 in at least one eye. The most frequently encountered ophthalmic complications included cystoid macular edema, cataract, and epiretinal membrane formation. Of 37 patients with pars planitis who had medical or neurologic follow-up evaluations, 6 (16.2%) developed multiple sclerosis. The HLA-DR15 allele, coding for one of the two HLA-DR2 subtypes, was associated with pars planitis (odds ratio = 2.86, 95% confidence interval = 1.42-5.78, P = 0.004). CONCLUSIONS: A common immunogenetic predisposition to multiple sclerosis and pars planitis may be associated with the HLA-DR15 allele. This association may represent genetic linkage to the HLA-DR locus or a role for the HLA-DR15 gene product in the pathogenesis of both of these diseases.
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Authors | S C Raja, D A Jabs, J P Dunn, S Fekrat, C H Machan, M J Marsh, N M Bressler |
Journal | Ophthalmology
(Ophthalmology)
Vol. 106
Issue 3
Pg. 594-9
(Mar 1999)
ISSN: 0161-6420 [Print] United States |
PMID | 10080220
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
- HLA-DR Antigens
- HLA-DR Serological Subtypes
- HLA-DR15 antigen
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Topics |
- Adolescent
- Adult
- Alleles
- Child
- Child, Preschool
- Cohort Studies
- Female
- Follow-Up Studies
- Gene Frequency
- Genetic Linkage
(genetics)
- HLA-DR Antigens
(genetics)
- HLA-DR Serological Subtypes
- Humans
- Male
- Middle Aged
- Multiple Sclerosis
(diagnosis, genetics)
- Optic Neuritis
(diagnosis, genetics)
- Pars Planitis
(diagnosis, genetics)
- Prognosis
- Visual Acuity
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