Anti-citrullinated peptide antibody-negative RA is a genetically distinct subset: a definitive study using only bone-erosive ACPA-negative rheumatoid arthritis

被引:62
作者
Ohmura, Koichiro [1 ]
Terao, Chikashi [2 ]
Maruya, Etsuko [3 ]
Katayama, Masaki
Matoba, Kenichiro [4 ]
Shimada, Kota [5 ]
Murasawa, Akira [6 ]
Honjo, Shigeru [7 ]
Takasugi, Kiyoshi [4 ]
Tohma, Shigeto [5 ]
Matsuo, Keitaro [8 ,9 ]
Tajima, Kazuo [8 ,9 ]
Yukawa, Naoichiro
Kawabata, Daisuke
Nojima, Takaki
Fujii, Takao
Yamada, Ryo [2 ]
Saji, Hiroo [3 ]
Matsuda, Fumihiko [2 ]
Mimori, Tsuneyo
机构
[1] Kyoto Univ, Dept Rheumatol & Clin Immunol, Grad Sch Med, Sakyo Ku, Kyoto 6068507, Japan
[2] Kyoto Univ, Grad Sch Med, Ctr Genom Med, Kyoto 6068507, Japan
[3] HLA Lab, Sakyo Ku, Kyoto, Japan
[4] Dohgo Spa Hosp, Dept Rheumatol, Matsuyama, Ehime, Japan
[5] Sagamihara Natl Hosp, Natl Hosp Org, Dept Rheumatol, Sagamihara, Kanagawa, Japan
[6] Niigata Rheumat Ctr, Dept Rheumatol, Niigata, Japan
[7] Saiseikai Takaoka Hosp, Dept Rheumatol, Toyama, Japan
[8] Aichi Canc Ctr Hosp, Div Epidemiol & Prevent, Nagoya, Aichi 464, Japan
[9] Aichi Canc Ctr, Res Inst, Chikusa Ku, Nagoya, Aichi 464, Japan
关键词
Rheumatoid arthritis; Anti-citrullinated peptide antibody; HLA; Shared epitope; Subset; Genetics; Association study; SHARED EPITOPE; ASSOCIATION; AUTOANTIBODIES; SUSCEPTIBILITY; HLA-DRB1; GENE; HYPOTHESIS; HAPLOTYPE; DIAGNOSIS; PROTEINS;
D O I
10.1093/rheumatology/keq273
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Methods. We genotyped HLA-DRB1 alleles for 574 ACPA-positive RA, 185 ACPA-negative RA (including 97 erosive RA) and 1508 healthy donors. We also tested whether HLA-DR SE is associated with RF-negative or ANA-negative RA. Results. ACPA-negative RA with apparent bone erosion was not associated with SE, supporting the idea that ACPA-negative RA is genetically distinct from ACPA-positive RA. We also tested whether these subsets are based on autoantibody-producing activity. In accordance with the ACPA-negative RA subset, the RF-negative RA subset showed a clearly distinct pattern of association with SE from the RF-positive RA. In contrast, ANA-negative as well as ANA-positive RA was similarly associated with SE, suggesting that the subsets distinguished by ACPA are not based simply on differences in autoantibody production. Conclusions. ACPA-negative erosive RA is genetically distinct from ACPA-positive RA.
引用
收藏
页码:2298 / 2304
页数:7
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