Genetic markers associated with cutaneous adverse drug reactions to allopurinol: aysystematic review

被引:2
|
作者
Jarjour, Samantha [1 ]
Barrette, Mathieu [1 ]
Normand, Valerie [2 ]
Rouleau, Jean Lucien [3 ,4 ]
Dube, Marie-Pierre [2 ,3 ,4 ]
de Denus, Simon [1 ,2 ,4 ]
机构
[1] Univ Montreal, Fac Pharm, Montreal, PQ H3T 1J4, Canada
[2] Univ Montreal, Beaulieu Saucier Pharmacogen Ctr, Montreal, PQ, Canada
[3] Univ Montreal, Fac Med, Montreal, PQ, Canada
[4] Montreal Heart Inst, Res Ctr, Montreal, PQ H1T 1C8, Canada
关键词
adverse reaction; allopurinol; drug-induced hypersensitivity syndrome; HLA; pharmacogenomics; rash; safety; Stevens-Johnson syndrome; toxic epidermal necrolysis; STEVENS-JOHNSON-SYNDROME; TOXIC EPIDERMAL NECROLYSIS; HAN CHINESE; HLA-B; HLA-B-ASTERISK-5801; ALLELE; RISK; POPULATION; GUIDELINES; THERAPY;
D O I
10.2217/PGS.15.21
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Pharmacogenomic markers in the HLA coding genes have been associated with drug hypersensitivity of multiple drugs, including allopurinol. In this systematic review, we summarize the pharmacogenomic evidence available regarding allopurinol-induced cutaneous adverse drug reactions (cADRs). We found that the HLA-B*5801 allele was significantly associated with the risk of severe cADRs in the Han Chinese, Korean, Thai, Japanese and European populations. The association between less severe cADRs and HLA-B*5801 was less consistent. All SNPs identified in genome-wide association studies of common variants were also located in or nearby HLA-B*5801. Future studies should focus on more common but less severe allopurinol-induced cADRs, as well as the potential role of rare variants as predictors of these cADRs.
引用
收藏
页码:755 / 767
页数:13
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