Min Fu-Li, Mao Bi-Jun, Zheng Zhong-Zheng, He Na, Fan Cui-Xia, Cai Rui-Yan, Wang Juan, Ou Yang-Mei, Qin Bing, Liao Wei-Ping, Yi Yong-Hong, Li Ze, Shi Yi-Wu
Institute of Neuroscience and Department of Neurology of the Second Affiliated Hospital of Guangzhou Medical University, Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Guangzhou, China.
Department of Neurology, Guangzhou First People's Hospital, School of Medicine, South China University of Technology, Guangzhou Medical University, Guangzhou, China.
Front Neurol. 2019 Jun 11;10:614. doi: 10.3389/fneur.2019.00614. eCollection 2019.
Antiepileptic drugs frequently cause cutaneous adverse reactions (cADRs). Numerous studies have reported associations between human leukocyte antigen (HLA) alleles and cADRs caused by single antiepileptic drug in Southern Han Chinese people. However, the relationship between the HLA allele and cADRs sequentially induced by two or more antiepileptic drugs (AEDs-induced cross-reactivity) is unclear. To explore the associations between HLA alleles and AEDs-induced cross-reactivity, we prospectively recruited patients with AEDs-induced cross-reactivity from 2009 to 2017 and performed high-resolution genotyping to detect the HLA-A, B, C, and DRB1 alleles in patients for comparison with normal controls. To verify the important genotype, we compared its presence in patients with cross-reactivity to enlarged normal controls, and its presence in patients with carbamazepine (CBZ)-induced maculopapular exanthema (MPE) to CBZ-tolerant controls. Further, the important allele was replicated by meta-analysis. Twenty-three patients with AED-induced cross-reactivity and 500 healthy individuals were enrolled from Southern China. All patients had a mild rash without mucosal or systemic involvement. The HLA-B13:01 allele was present in 34.78% (8/23) of patients, 14.60% (73/500) of healthy individuals, and 14.5% (763/5,270) healthy individuals, revealing a significant association (8/23 vs. 73/500; = 0.02; OR: 3.12; 95% CI: 1.28-7.62; 8/23 vs. 763/5,270; = 0.014; OR: 3.15; 95% CI: 1.33-7.46). HLA-B13:01 was presented numerically higher in CBZ-induced MPE than that in CBZ-tolerant individuals without statistical significance (33/145, 22.76%, vs. 28/179, 15.64%; = 0.103). Meta-analysis revealed an association between HLA-B13:01 and cADRs induced by single AEDs or/and non-AEDs in Chinese and Thai populations ( = 0.000). This study suggests that HLA-B13:01 is potentially associated with AED-cADRs in general, possibly with stronger effect in cross-reactivity. Screening for HLA-B13:01 prior to starting AEDs therapy may help to avoid cADRs. However, this association requires further analysis in a multi-center study with a larger sample size.
抗癫痫药物常引起皮肤不良反应(cADRs)。众多研究报道了人类白细胞抗原(HLA)等位基因与中国南方汉族人群中单一抗癫痫药物所致cADRs之间的关联。然而,HLA等位基因与两种或更多种抗癫痫药物序贯诱导的cADRs(抗癫痫药物诱导的交叉反应性)之间的关系尚不清楚。为了探究HLA等位基因与抗癫痫药物诱导的交叉反应性之间的关联,我们在2009年至2017年期间前瞻性招募了抗癫痫药物诱导交叉反应性的患者,并进行高分辨率基因分型以检测患者的HLA - A、B、C和DRB1等位基因,以便与正常对照进行比较。为了验证重要的基因型,我们将其在交叉反应性患者中的存在情况与扩大的正常对照进行比较,并将其在卡马西平(CBZ)诱导的斑丘疹(MPE)患者中的存在情况与CBZ耐受对照进行比较。此外,通过荟萃分析对重要等位基因进行了重复验证。从中国南方招募了23例抗癫痫药物诱导交叉反应性的患者和500名健康个体。所有患者均有轻度皮疹,无黏膜或全身受累。HLA - B13:01等位基因在23例患者中的占比为34.78%(8/23),在500名健康个体中的占比为14.60%(73/500),在5270名健康个体中的占比为14.5%(763/5270),显示出显著关联(8/23 vs. 73/500;P = 0.02;OR:3.12;95%CI:1.28 - 7.62;8/23 vs. 763/5270;P = 0.014;OR:3.15;95%CI:1.33 - 7.46)。HLA - B13:01在CBZ诱导的MPE中的数值高于CBZ耐受个体,但无统计学意义(145例中有33例,2