Association of HLA shared epitope with joint damage progression in rheumatoid arthritis

Citation
A. Valenzuela et al., Association of HLA shared epitope with joint damage progression in rheumatoid arthritis, HUMAN IMMUN, 60(3), 1999, pp. 250-254
Citations number
15
Categorie Soggetti
Immunology
Journal title
HUMAN IMMUNOLOGY
ISSN journal
01988859 → ACNP
Volume
60
Issue
3
Year of publication
1999
Pages
250 - 254
Database
ISI
SICI code
0198-8859(199903)60:3<250:AOHSEW>2.0.ZU;2-D
Abstract
A nine years prospective study was performed on 82 Spanish rheumatoid arthr itis patients with a disease duration of less than two years at the study e ntry, in order to evaluate the role of HLA markers in the susceptibility an d progression of rheumatoid arthritis. Radiological evaluation of disease s everity was performed at the time of diagnosis and 9 years later. High reso lution HLA-DR typing demonstrated chat the presence of the shared epitope ( SE) was more frequent among patients (61% vs. 31% in controls; P = 0.00003; OR = 3.48). Fourteen patients carried two SE+ HLA-DRB1 alleles (Si +/+); 3 6, one single allele (SE +/-) and 32 were SE negative(SE -/-). HLA-DR4 (par ticularly DRB1*0401 and DRB1*0405) and HLA-DR10 were increased among patien ts. Ar study entry, the frequencies of locally severe (hands and feet) RA w ere more frequent among SE +/+ patients (79%) than among SE +/- (47%) and S E -/- (44%) patients (p = 0.05; RR = 1.80). After 3 years of disease these differences disappeared, where as differences in the extent of the disease arise: 79%, 50% and 32% of SE +/+, SE +/- and SE -/- patients respectively showed large joints involvement (shoulders, elbows, hips and knees) (p = 0. 01; RR = 2.44 for SE+/+ vs. SE -/-; and p = 0.04; RR = 1.81 for SE+ vs. SE- ). These results suggest that the presence of the shared epitope is associa ted with the extent and progression of radiological joint damage in rheumat oid arthritis. Human Immunology 60, 250-254 (1999). (C) American Society fo r Histocompatibility and Immunogenetics, 1999. Published by Elsevier Scienc e Inc.