Department of Dermatology, Huashan Hospital, Fudan University, Shanghai, China.
Department of Pharmacology, School of Medicine, Zhengzhou University, Zhengzhou, China.
Basic Clin Pharmacol Toxicol. 2018 Sep;123(3):308-313. doi: 10.1111/bcpt.13011. Epub 2018 Apr 25.
Genetic risk factors could cause cutaneous adverse drug reactions (cADRs) in patients after treatment with clarithromycin. This study explored the association of HLA class I genes with clarithromycin-cADRs in Han Chinese patients. A total of 12 clarithromycin-cADR patients and 34 clarithromycin-tolerant controls were recruited for the high-resolution genotyping of HLA class I genes (HLA-A, HLA-B and HLA-C). The population controls consisted of 283 Han Chinese retrieved from the MHC database for validated comparison. A molecular docking analysis of HLA-A02:07 protein and clarithromycin was conducted using glide module with Schrödinger Suite. Among all tested HLA alleles, the carrier frequencies of HLA-A02:07 (58% versus 5.9%, OR = 22.40, 95% CI = 3.58-139.98, p = 8.20 × 10E-5, pc = 1.1 × 10E-3) and HLA-B46:01 (50% versus 5.9%, OR = 16.00, 95% CI = 2.59-98.99, p = 0.002, pc = 0.03) were significantly higher in clarithromycin-cADRs than in clarithromycin-tolerant controls. However, when compared to population controls, only HLA-A02:07, and not HLA-B46:01, reached statistical significance (58% versus 15.5%, OR = 7.61, 95% CI = 2.31-25.04, p = 1.2 × 10E-4, pc = 1.7 × 10E-3). Furthermore, molecular docking data revealed that clarithromycin could bind to and interact with HLA-A02:07 in two possible binding situations. These data suggest that HLA-A*02:07 might be a genetic risk factor for developing clarithromycin-cADRs in Han Chinese and serve as a useful biomarker for personalized medicine to prevent clarithromycin-cADRs.
遗传风险因素可能导致使用克拉霉素治疗后的患者出现皮肤药物不良反应(cADR)。本研究旨在探讨人类白细胞抗原(HLA)I 类基因与汉族患者克拉霉素-cADR 的相关性。共招募了 12 名克拉霉素-cADR 患者和 34 名克拉霉素耐受对照者进行 HLA I 类基因(HLA-A、HLA-B 和 HLA-C)高分辨率基因分型。人群对照者来自 MHC 数据库中的 283 名汉族个体,用于验证比较。使用 Schrödinger Suite 中的 glide 模块对 HLA-A02:07 蛋白和克拉霉素进行分子对接分析。在所有检测的 HLA 等位基因中,HLA-A02:07 的携带频率(58%比 5.9%,OR=22.40,95%CI=3.58-139.98,p=8.20×10E-5,pc=1.1×10E-3)和 HLA-B46:01(50%比 5.9%,OR=16.00,95%CI=2.59-98.99,p=0.002,pc=0.03)在克拉霉素-cADR 患者中明显高于克拉霉素耐受对照者。然而,与人群对照者相比,仅 HLA-A02:07,而不是 HLA-B46:01,达到统计学意义(58%比 15.5%,OR=7.61,95%CI=2.31-25.04,p=1.2×10E-4,pc=1.7×10E-3)。此外,分子对接数据显示克拉霉素可以与 HLA-A02:07 结合并在两种可能的结合情况下相互作用。这些数据表明,HLA-A*02:07 可能是汉族患者发生克拉霉素-cADR 的遗传风险因素,可作为预防克拉霉素-cADR 的个体化医学的有用生物标志物。