HLA-DRB1 typing in rheumatoid arthritis: predicting response to specific treatments

被引:98
作者
O'Dell, JR
Nepom, BS
Haire, C
Gersuk, VH
Gaur, L
Moore, GF
Drymalski, W
Palmer, W
Eckhoff, PJ
Klassen, LW
Wees, S
Thiele, G
Nepom, GT
机构
[1] Univ Nebraska, Med Ctr, Dept Internal Med, Omaha, NE 68198 USA
[2] Omaha Vet Affairs Med Ctr, Omaha, NE USA
[3] Virginia Mason Res Ctr, Seattle, WA 98101 USA
关键词
D O I
10.1136/ard.57.4.209
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective-To determine the predictive value of shared epitope alleles for response to treatment in patients with rheumatoid arthritis. Methods-Patients from our previously published triple DIMARD study were tested for the presence of shared epitope alleles (DRB1 star 0401,0404/0408, 0405,0101, 1001,and 1402). Patients who were shared epitope positive were then compared with those who were negative to see if there was a differential effect on therapeutic response. Results-Shared epitope positive patients were much more likely to achieve a 50% response if treated with methotrexate-sulphasalazine-hydroxychloroquine compared with methotrexate alone (94% responders versus 32%, p<0.0001). In contrast shared epitope negative patients did equally well regardless of treatment (88% responders for methotrexate-sulphasalazine-hydroxychloroquine versus 83% for methotrexate). Additionally, a trend toward an inverse relation of the gene dose was seen for response to methotrexate treatment (p=0.05). Conclusions-These data suggest that determining shared epitope status may provide clinical information useful in selecting among treatment options.
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收藏
页码:209 / 213
页数:5
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