Impact of the HLA-B*58:01 Allele and Renal Impairment on Allopurinol-Induced Cutaneous Adverse Reactions

被引:66
作者
Ng, Chau Yee [1 ,2 ,3 ,4 ]
Yeh, Yu-Ting [1 ,2 ,3 ,4 ]
Wang, Chuang-Wei [1 ,2 ,3 ,5 ,6 ]
Hung, Shuen-Iu [7 ]
Yang, Chih-Hsun [1 ,2 ,3 ,4 ]
Chang, Ya-Ching [1 ,2 ,3 ,4 ]
Chang, Wan-Chun [7 ]
Lin, Yu-Jr [8 ,9 ]
Chang, Chee-Jen [8 ,9 ]
Su, Shih-Chi [1 ,2 ,3 ,13 ]
Fan, Wen-Lang [13 ]
Chen, Der-Yuan [10 ]
Wu, Yeong-Jian Jan [4 ,11 ]
Tian, Ya-Chung [12 ]
Hui, Rosaline Chung-Yee [1 ,2 ,3 ,4 ]
Chung, Wen-Hung [1 ,2 ,3 ,4 ,5 ,6 ,13 ]
机构
[1] Chang Gung Mem Hosp, Drug Hypersensit Clin & Res Ctr, Dept Dermatol, Taipei, Taiwan
[2] Chang Gung Mem Hosp, Drug Hypersensit Clin & Res Ctr, Dept Dermatol, Linkou, Taiwan
[3] Chang Gung Mem Hosp, Drug Hypersensit Clin & Res Ctr, Dept Dermatol, Keelung, Taiwan
[4] Chang Gung Univ, Sch Med, Coll Med, Taoyuan, Taiwan
[5] Chang Gung Mem Hosp, Chang Gung Immunol Consortium, Taoyuan, Taiwan
[6] Chang Gung Univ, Taoyuan, Taiwan
[7] Natl Yang Ming Univ, Inst Pharmacol, Sch Med, Taipei, Taiwan
[8] Chang Gung Univ, Grad Inst Clin Med Sci, Clin Informat & Med Stat Res Ctr, Taoyuan, Taiwan
[9] Chang Gung Mem Hosp, Biostat Ctr Clin Res, Linkou, Taiwan
[10] Taichung Vet Gen Hosp, Dept Rheumatol, Taichung, Taiwan
[11] Chang Gung Mem Hosp, Dept Med, Div Allergy Immunol & Rheumatol, Keelung, Taiwan
[12] Chang Gung Univ, Chang Gung Mem Hosp, Dept Nephrol, Kidney Res Ctr, Taoyuan, Taiwan
[13] Chang Gung Mem Hosp, Whole Genome Res Core, Lab Human Dis, Keelung, Taiwan
关键词
STEVENS-JOHNSON-SYNDROME; TOXIC EPIDERMAL NECROLYSIS; HYPERSENSITIVITY SYNDROME; DRESS SYNDROME; HLA-B; ASSOCIATION; RISK; MANAGEMENT; PROGRESSION; THERAPY;
D O I
10.1016/j.jid.2016.02.808
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Allopurinol, a common drug for treating hyperuricemia, is associated with cutaneous adverse drug reactions ranging from mild maculopapular exanthema to life-threatening severe cutaneous adverse reactions, including drug reaction with eosinophilia and systemic symptoms, Stevens-Johnson syndrome, and toxic epidermal necrolysis. We have previously reported that HLA-B*58:01 is strongly associated with allopurinol-induced severe cutaneous adverse reactions in Han Chinese, but the associations of the HLA-B*58:01 genotype in an allopurinol-induced hypersensitivity phenotype remain unclear. To investigate the comprehensive associations of HLA-B*58:01, we enrolled 146 patients with allopurinol-induced cutaneous adverse drug reactions (severe cutaneous adverse reactions, n = 106; maculopapular exanthema, n = 40) and 285 allopurinol-tolerant control subjects. Among these allopurinol-induced cutaneous adverse drug reactions, HLA-B*58:01 was strongly associated with severe cutaneous adverse reactions (odds ratio [OR] = 44.0; 95% confidence interval = 21.5-90.3; P = 2.6 x 10(-41)), and the association was correlated with disease severity (OR = 44.0 for severe cutaneous adverse reactions, OR = 8.5 for maculopapular exanthema). The gene dosage effect of HLA-B*58:01 also influenced the development of allopurinol-induced cutaneous adverse drug reactions (OR = 15.25 for HLA-B*58:01 heterozygotes and OR = 72.45 for homozygotes). Furthermore, coexistence of HLA-B*58:01 and renal impairment increased the risk and predictive accuracy of allopurinol-induced cutaneous adverse drug reactions (heterozygous HLA-B*58:01 and normal renal function:OR = 15.25, specificity = 82%; homozygous HLA-B*58:01 and severe renal impairment:OR = 1269.45, specificity = 100%). This HLA-B*58:01 correlation study suggests that patients with coexisting HLA-B*58:01 and renal impairment (especially estimated glomerular filtration rate <30ml/minute/1.73 m(2)) should be cautious and avoid using allopurinol.
引用
收藏
页码:1373 / 1381
页数:9
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