Genetic susceptibility and the link between cat exposure and rheumatoid arthritis

Citation
Ps. Penglis et al., Genetic susceptibility and the link between cat exposure and rheumatoid arthritis, SEM ARTH RH, 30(2), 2000, pp. 111-120
Citations number
36
Categorie Soggetti
Rheumatology
Journal title
SEMINARS IN ARTHRITIS AND RHEUMATISM
ISSN journal
00490172 → ACNP
Volume
30
Issue
2
Year of publication
2000
Pages
111 - 120
Database
ISI
SICI code
0049-0172(200010)30:2<111:GSATLB>2.0.ZU;2-#
Abstract
Objectives: Rheumatoid arthritis (RA) is a chronic inflammatory disease for which immunogenetic susceptibility factors have been defined. In a recent case control study, it was shown that a prior intimate relationship with pe t cats or budgerigars confers risk for subsequent development of RA after a period of latency. Pets are a potential reservoir for putative microbial a gents that could be a stimulus for chronic inflammation subject to the infl uence of immunogenetic factors. Therefore, a study was undertaken to determ ine whether the presence of HLA-DRB1 alleles bearing the RA susceptibility motif influenced risk for RA associated with prior exposure to pets. Methods: Blood samples were obtained from available RA patients and their c ase controls who had participated in the prior epidemiologic study. DR and DQ genotypes were determined by sequence analysis of oligonucleotides ampli fied from the DRB1 and DQB1 genes by polymerase chain reactions (PCR). Subj ects were segregated according to pet exposure (as determined previously) a nd genotype for statistical analyses. Results: The odds ratio (OR) for prepubertal exposure to cats and RA in ava ilable subjects irrespective of DRB1 genotype was 4.2 (CI, 2.1 to 8.5; P < .00002). The OR between prior exposure to cats and RA in subjects with the RA susceptibility genotype DRB1 *0401 and *0404 was 5.8 (CI, 1.4 to 26; P < .02) and >24 (CI, 1.6 to 813; P < .01), respectively. In subjects with the genotype DRB1 *1501, the association between RA and prior cat exposure was OR 8.4 (CI, 1.7 to 45; P < .01). No significant association between RA and pet exposure was found in patients selected according to other genotypes. The association between RA and the recognized HLA-DR susceptibility motif w as slightly stronger in subjects with a history of intimate cat exposure (O R 4.7 [CI, 1.5 to 14.8], P < .005) than subjects without prior intimate exp osure (OR 3.3 [CI; 1.2 to 9.3], P < .02). In the small number of subjects w ho had reported an intimate association with pet birds, no influence of DR genotype on risk for RA was discerned. Conclusions: Risk for RA associated with prior intimate exposure to cats is concentrated in subjects with the RA-susceptibility conferring genotypes D RB1 *0401 and *0404. The findings suggest an interaction between an environ mental agent associated with pet cats and certain RA susceptibility-conferr ing DR genotypes. The risk for RA associated with intimate cat exposure als o was significant in subjects with DRB1*1501, a genotype not otherwise asso ciated with RA, but which shares with known RA susceptibility-bearing allel es the presence of an electropositive pocket (Pocket 4) in the DR peptide b inding groove. Copyright (C) 2000 by W.B. Saunders Company.