Chen Chun-Bing, Hsiao Yi-Hsin, Wu Tony, Hsih Mo-Song, Tassaneeyakul Wichittra, Jorns Teekayu P, Sukasem Chonlaphat, Hsu Chien-Ning, Su Shih-Chi, Chang Wan-Chun, Hui Rosaline Chung-Yee, Chu Chia-Yu, Chen Yi-Ju, Wu Ching-Ying, Hsu Chao-Kai, Chiu Tsu-Man, Sun Pei-Lun, Lee Hua-En, Yang Chin-Yi, Kao Pei-Han, Yang Chih-Hsun, Ho Hsin-Chun, Lin Jing-Yi, Chang Ya-Ching, Chen Ming-Jing, Lu Chun-Wei, Ng Chau Yee, Kuo Kang-Ling, Lin Chien-Yio, Yang Ching-Sheng, Chen Ding-Ping, Chang Pi-Yueh, Wu Tsu-Lan, Lin Yu-Jr, Weng Yi-Ching, Kuo Tseng-Tong, Hung Shuen-Iu, Chung Wen-Hung
Authors' affiliations are listed at the end of the article.
Neurology. 2017 Jan 3;88(1):78-86. doi: 10.1212/WNL.0000000000003453. Epub 2016 Dec 2.
To investigate the risk and genetic association of oxcarbazepine-induced cutaneous adverse reactions (OXC-cADRs), including Stevens-Johnson syndrome/toxic epidermal necrolysis (SJS/TEN), in Asian populations (Chinese and Thai).
We prospectively enrolled patients with OXC-cADRs in Taiwan and Thailand from 2006 to 2014, and analyzed the clinical course, latent period, drug dosage, organ involvement, complications, and mortality. We also investigated the carrier rate of HLA-B15:02 and HLA-A31:01 of patients with OXC-cADRs and compared to OXC-tolerant controls. The incidence of OXC-SJS/TEN was compared with carbamazepine (CBZ)-induced SJS/TEN according to the nationwide population dataset from the Taiwan National Health Insurance Research Database.
We enrolled 50 patients with OXC-cADRs, including 20 OXC-SJS/TEN and 6 drug reaction with eosinophilia and systemic symptoms, of Chinese patients from Taiwan and Thai patients from Thailand. OXC-cADRs presented with less clinical severity including limited skin detachment (all ≦5%) and no mortality. There was a significant association between HLA-B15:02 and OXC-SJS (p = 1.87 × 10; odds ratio 27.90; 95% confidence interval [CI] 7.84-99.23) in Chinese and this significant association was also observed in Thai patients. The positive and negative predictive values of HLA-B15:02 for OXC-SJS/TEN were 0.73% and 99.97%, respectively. HLA-A*31:01 was not associated with OXC-cADRs. The incidence and mortality of OXC-SJS/TEN was lower than CBZ-STS/TEN in new users (p = 0.003; relative risk 0.212; 95% CI 0.077-0.584).
Our findings suggest that HLA-B15:02 is significantly associated with OXC-SJS in Asian populations (Chinese and Thai). However, the severity and incidence of OXC-SJS/TEN are less than that of CBZ-SJS/TEN. The need for preemptive HLA-B15:02 screening should be evaluated further.
在亚洲人群(中国和泰国)中,调查奥卡西平诱发的皮肤不良反应(OXC-cADRs)的风险及遗传关联,包括史蒂文斯-约翰逊综合征/中毒性表皮坏死松解症(SJS/TEN)。
我们前瞻性纳入了2006年至2014年在台湾和泰国患有OXC-cADRs的患者,分析其临床病程、潜伏期、药物剂量、器官受累情况、并发症及死亡率。我们还调查了OXC-cADRs患者中HLA-B15:02和HLA-A31:01的携带率,并与耐受奥卡西平的对照组进行比较。根据台湾国民健康保险研究数据库的全国人口数据集,比较奥卡西平-SJS/TEN与卡马西平(CBZ)诱发的SJS/TEN的发生率。
我们纳入了50例患有OXC-cADRs的患者,包括20例OXC-SJS/TEN患者以及6例伴有嗜酸性粒细胞增多和全身症状的药物反应患者,这些患者来自台湾的中国患者和泰国的泰国患者。OXC-cADRs的临床严重程度较低,包括皮肤剥脱范围有限(均≤5%)且无死亡病例。在中国人群中,HLA-B15:02与OXC-SJS之间存在显著关联(p = 1.87×10;比值比27.90;95%置信区间[CI] 7.84 - 99.23),在泰国患者中也观察到了这种显著关联。HLA-B15:02对OXC-SJS/TEN的阳性预测值和阴性预测值分别为0.73%和99.97%。HLA-A*31:01与OXC-cADRs无关。新使用者中奥卡西平-SJS/TEN的发生率和死亡率低于CBZ-STS/TEN(p = 0.003;相对风险0.212;95% CI 0.077 - 0.584)。
我们的研究结果表明,在亚洲人群(中国和泰国)中,HLA-B15:02与OXC-SJS显著相关。然而,奥卡西平-SJS/TEN的严重程度和发生率低于卡马西平-SJS/TEN。对HLA-B15:02进行预防性筛查的必要性应进一步评估。