Department of Laboratory Medicine, West China Hospital, Sichuan University, Chengdu, China.
Microbiol Immunol. 2021 Apr;65(4):143-153. doi: 10.1111/1348-0421.12877. Epub 2021 Mar 24.
Antituberculosis drug-induced liver injury (ATDILI) has received increasing attention globally, which may limit the effectiveness of antituberculosis (anti-TB) treatment. Many host genetic determinants of ATDILI have been identified recently. As little knowledge is currently available about the association between aldehyde dehydrogenase 1 family member A1 (ALDH1A1) polymorphisms and ATDILI, the association between their variants and the susceptibility to ATDILI was investigated. A total of 747 patients with TB treated by first-line anti-TB drugs were prospectively enrolled at West China Hospital. Genomic DNA was extracted from the peripheral blood sample of each patient and seven single-nucleotide polymorphisms (SNPs) of ALDH1A1 gene were screened and genotyped with a custom-designed 2×48-plex SNP Scan TM kit. The patients were followed up monthly to monitor the development of ATDILI. The C allele and the CA genotype of rs7852860 were significantly associated with an elevated risk for ATDILI (p = .006 and 0.005, respectively), which was consistent with the results in the dominant and additive models. No allele, genotype, or genetic model of the other six SNPs (rs3764435, rs348471, rs63319, rs610529, rs7027604, rs8187876) were found to be associated with susceptibility to ATDILI. The findings first demonstrate that rs7852860 variants in ALDH1A1 gene is associated with susceptibility to ATDILI in the Chinese Han population. Validation studies with larger sample sizes and other ethnic groups are needed to confirm the findings.
抗结核药物性肝损伤(ATDILI)在全球范围内受到越来越多的关注,这可能会限制抗结核(抗-TB)治疗的效果。最近已经确定了许多宿主遗传决定因素与 ATDILI 相关。由于目前对于醛脱氢酶 1 家族成员 A1(ALDH1A1)基因多态性与 ATDILI 之间的关联知之甚少,因此研究了它们的变体与 ATDILI 易感性之间的关联。华西医院前瞻性纳入了 747 例接受一线抗结核药物治疗的结核病患者。从每位患者的外周血样本中提取基因组 DNA,并使用定制的 2×48-plex SNP Scan™试剂盒筛选和基因分型 ALDH1A1 基因的 7 个单核苷酸多态性(SNP)。每月对患者进行随访以监测 ATDILI 的发生。rs7852860 的 C 等位基因和 CA 基因型与 ATDILI 风险升高显著相关(p=0.006 和 0.005),这与显性和加性模型的结果一致。其他六个 SNPs(rs3764435、rs348471、rs63319、rs610529、rs7027604、rs8187876)的等位基因、基因型或遗传模型均与 ATDILI 易感性无关。这些发现首次表明,ALDH1A1 基因中的 rs7852860 变体与中国汉族人群中 ATDILI 的易感性相关。需要更大样本量和其他种族的验证研究来证实这些发现。