Relationship between CYP2E1 Gene Polymorphism and Anti-tuberculosis Drug-induced Liver Injury

Donglin Zhu, Yun Xi, Jie-Ming Dong, F. Huang, Changzhi Xu, G. Xiao
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Abstract

 Objective: To investigate the relationship between cytochrome P450 E1 (CYP2E1) gene polymorphisms and susceptibility to anti-tuberculosis drug-induced liver damage (ATDLI) in tuberculosis patients in the Chinese Han nationality. Methods: A retrospective analysis was performed on 360 patients with tuberculosis who had liver damage after tuberculosis treatment (case group) and 360 patients with tuberculosis who did not develop liver injury after treatment (control group). MassARRAY were used to detect CYP2E1 gene polymorphisms. Results: In a total of 8 tagged SNP loci selected, the rs8192773 locus failed to pass the test, and therefore, it is not included in subsequent analysis. At the remaining seven SNP sites, the difference in alleles was not statistically significant between the case group and the control group, suggesting that these sites may not be related to liver damage caused by anti-tuberculosis drugs. Three monomer domains were found in the seven tags SNP loci mentioned above. However, it was found that these haplotypes are not closely related to anti-tuberculosis drug-induced liver damage. Conclusion: The CYP2E1 gene polymorphism in the Chinese Han nationality is not related to the occurrence of anti-tuberculosis drug-induced liver injury.
CYP2E1基因多态性与抗结核药物性肝损伤的关系
目的:探讨中国汉族结核病患者细胞色素P450 E1 (CYP2E1)基因多态性与抗结核药物性肝损害(ATDLI)易感性的关系。方法:回顾性分析360例结核治疗后出现肝损伤的结核患者(病例组)和360例治疗后未出现肝损伤的结核患者(对照组)。使用MassARRAY检测CYP2E1基因多态性。结果:在选择的8个标记SNP位点中,rs8192773位点未通过检测,因此不纳入后续分析。其余7个SNP位点,病例组与对照组的等位基因差异无统计学意义,提示这些位点可能与抗结核药物引起的肝损害无关。在上述7个标签SNP位点中发现了3个单体结构域。然而,我们发现这些单倍型与抗结核药物引起的肝损害关系并不密切。结论:中国汉族CYP2E1基因多态性与抗结核药物性肝损伤的发生无关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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