Association between HLA-B*1502 and carbamazepine-induced severe cutaneous adverse drug reactions in a Thai population

被引:233
作者
Tassaneeyakul, Wichittra [1 ]
Tiamkao, Somsak [2 ]
Jantararoungtong, Thawinee
Chen, Pei [3 ]
Lin, Shu-Yi [3 ]
Chen, Wei-Hsuan [3 ]
Konyoung, Parinya [4 ]
Khunarkornsiri, Usanee [4 ]
Auvichayapat, Narong [5 ]
Pavakul, Kasemsin [6 ]
Kulkantrakorn, Kongkiat [7 ]
Choonhakarn, Charoen [2 ]
Phonhiamhan, Siranun [8 ]
Piyatrakul, Namfon [9 ]
Aungaree, Thiti [10 ]
Pongpakdee, Sunsanee [11 ]
Yodnopaglaw, Praphan [12 ]
机构
[1] Khon Kaen Univ, Fac Med, Dept Pharmacol, Khon Kaen 40002, Thailand
[2] Khon Kaen Univ, Dept Med, Khon Kaen 40002, Thailand
[3] Acad Sinica, Inst Biomed Sci, Taipei, Taiwan
[4] Udonthani Hosp, Pharm Unit, Udonthani, Thailand
[5] Khon Kaen Univ, Fac Med, Dept Pediat, Khon Kaen 40002, Thailand
[6] Khon Kaen Hosp, Dept Med, Khon Kaen, Thailand
[7] Thammasat Univ, Fac Med, Dept Med, Pathum Thani, Thailand
[8] Nakhonphanom Hosp, Pharm Unit, Nakhonphanom, Thailand
[9] Suanprung Psychiat Hosp, Pharm Unit, Chiangmai, Thailand
[10] Udonthani Hosp, Dept Med, Udonthani, Thailand
[11] Royal Thai AF, Bhumibol Adulyadej Hosp, Dept Med, Bangkok, Thailand
[12] Surin Hosp, Dept Med, Surin, Thailand
关键词
HLA-B*1502; Carbamazepine; Severe cutaneous adverse drug reactions; Stevens-Johnson syndrome (S[!text type='JS']JS[!/text]); Toxic epidermal necrolysis (TEN); STEVENS-JOHNSON-SYNDROME; TOXIC EPIDERMAL NECROLYSIS; ALLELE; MARKER; RISK;
D O I
10.1111/j.1528-1167.2010.02533.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
P>Carbamazepine (CBZ) has been reported as the most common culprit drug for Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) in several Asian countries including Thailand. A strong association between HLA-B*1502 and CBZ-induced SJS/TEN has been reported in Han Chinese but not in Caucasian and Japanese populations. A case-control study was conducted to determine whether HLA-B*1502 is a valid pharmacogenetic test for SJS/TEN caused by CBZ in a Thai population. Among 42 CBZ-induced patients with SJS/TEN, 37 (88.10%) patients carried the HLA-B*1502 while only 5 (11.90%) of the CBZ-tolerant controls had this allele. The risk of CBZ-induced SJS/TEN was significantly higher in the patients with HLA-B*1502, with an odds ratio (OR) of 54.76 [95% confidence interval (CI) 14.62-205.13, p = 2.89 x 10-12]. The sensitivity and specificity of HLA-B*1502 for prediction of CBZ-induced SJS/TEN were 88.10%. By assuming a 0.27% as a prevalence rate of CBZ-induced SJS/TEN in a Thai population, the positive predictive value (PPV) and negative predictive value (NPV) of the HLA-B*1502 were 1.92% and 99.96%. Results from this study suggest that HLA-B*1502 may be a useful pharmacogenetic test for screening Thai individuals who may be at risk for CBZ-induced SJS and TEN.
引用
收藏
页码:926 / 930
页数:5
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