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Independent association of HLA-DPB1*02:01 with rheumatoid arthritis in Japanese populations

OBJECTIVE: Rheumatoid arthritis (RA) is a chronic autoimmune disease characterized with joint destructions; environmental and genetic factors were thought to be involved in the etiology of RA. The production of anti-citrullinated peptide antibodies (ACPA) is specifically associated with RA. DRB1 is...

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Detalles Bibliográficos
Autores principales: Furukawa, Hiroshi, Oka, Shomi, Shimada, Kota, Hashimoto, Atsushi, Komiya, Akiko, Tsunoda, Shinichiro, Suda, Akiko, Ito, Satoshi, Saisho, Koichiro, Katayama, Masao, Shinohara, Satoshi, Sato, Takeo, Nagatani, Katsuya, Minota, Seiji, Matsui, Toshihiro, Fukui, Naoshi, Sugii, Shoji, Sano, Hajime, Migita, Kiyoshi, Nagaoka, Shouhei, Tohma, Shigeto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6157818/
https://www.ncbi.nlm.nih.gov/pubmed/30235330
http://dx.doi.org/10.1371/journal.pone.0204459
Descripción
Sumario:OBJECTIVE: Rheumatoid arthritis (RA) is a chronic autoimmune disease characterized with joint destructions; environmental and genetic factors were thought to be involved in the etiology of RA. The production of anti-citrullinated peptide antibodies (ACPA) is specifically associated with RA. DRB1 is associated with the susceptibility of RA, especially ACPA-positive RA [ACPA(+)RA]. However, a few studies reported on the independent associations of DPB1 alleles with RA susceptibility. Thus, we investigated the independent association of DPB1 alleles with RA in Japanese populations. METHODS: Association analyses of DPB1 were conducted by logistic regression analysis in 1667 RA patients and 413 controls. RESULTS: In unconditioned analysis, DPB1*04:02 was nominally associated with the susceptibility of ACPA(+)RA (P = 0.0021, corrected P (Pc) = 0.0275, odds ratio [OR] 1.52, 95% confidence interval [CI] 1.16–1.99). A significant association of DPB1*02:01 with the susceptibility of ACPA(+)RA was observed, when conditioned on DRB1 (P(adjusted) = 0.0003, Pc(adjusted) = 0.0040, OR(adjusted) 1.47, 95%CI 1.19–1.81). DPB1*05:01 was tended to be associated with the protection against ACPA(+)RA, when conditioned on DRB1 (P(adjusted) = 0.0091, Pc(adjusted) = 0.1184, OR(adjusted) 0.78, 95%CI 0.65–0.94). When conditioned on DRB1, the association of DPB1*04:02 with ACPA(+)RA was disappeared. No association of DPB1 alleles with ACPA-negative RA was detected. CONCLUSION: The independent association of DPB1*02:01 with Japanese ACPA(+)RA was identified.