The relationship between HLA-DRB1 alleles and disease subsets of rheumatoid arthritis in Japanese

被引:0
|
作者
Wakitani, S
Murata, N
Toda, Y
Ogawa, R
Kaneshige, T
Nishimura, Y
Ochi, T
机构
[1] KANSAI MED UNIV, OTOKOYAMA HOSP, DEPT ORTHOPAED SURG, YAHATA 614, JAPAN
[2] KANSAI MED UNIV, DEPT ORTHOPAED SURG, MORIGUCHI, OSAKA 570, JAPAN
[3] SHIONOGI BIOMED LABS, SETTSU 566, JAPAN
[4] KUMAMOTO UNIV, GRAD SCH MED SCI, DEPT NEUROSCI & IMMUNOL, KUMAMOTO 860, JAPAN
[5] OSAKA UNIV, SCH MED, DEPT ORTHOPAED SURG, SUITA, OSAKA 565, JAPAN
来源
BRITISH JOURNAL OF RHEUMATOLOGY | 1997年 / 36卷 / 06期
关键词
HLA; RA; shared epitope; disease severity;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
To assess the association between HLA-DRB1 and the pathogenesis of rheumatoid arthritis (RA) in the Japanese population, we typed for HLA-DRB1 alleles in 852 Japanese patients. An analysis of HLA-DRB1 allele associations was performed on the overall group and in three disease subsets of adult-onset RA, classified according to the extent of joint destruction evident on plain radiograms, i.e. least erosive subset (LES), more erosive subset (MES) and most erosive subset with mutilating disease (MUD). The Japanese RA patients were positively associated with DRB1*0101 and *0405, and negatively associated with DRB1*0701, *0802, *1302 and *1405. DRB1*0101 was associated more strongly with a milder disease subset and the relative risk (RR) was 1.9, 1.5 and 1.2 for LES, MES and MUD, respectively. On the other hand, DRB1*0405 was associated more strongly with a more severe disease subset, the RR being 1.8, 4.0 and 4.3 for LES, MES and MUD, respectively. These findings suggest that RA is a heterogeneous disease, not only clinically, but also in terms of its immunogenetic background, and that HLA-DRB1 can be a useful prognostic factor for RA.
引用
收藏
页码:630 / 636
页数:7
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