HMOX1型
单核苷酸多态性
血红素
医学
基因分型
邦费罗尼校正
SNP公司
人口
病例对照研究
UGT2B7型
药理学
血红素加氧酶
基因型
基因
生物
内科学
遗传学
血红素
葡萄糖醛酸化
生物化学
数学
环境卫生
酶
体外
微粒体
统计
作者
Wenpei Liu,Lihuan Lu,Hongqiu Pan,Xiaomin He,Meiling Zhang,Nannan Wang,Jia Zhu,Honggang Yi,Shaowen Tang
出处
期刊:Pharmacogenomics
[Future Medicine]
日期:2022-04-26
卷期号:23 (7): 431-441
被引量:4
标识
DOI:10.2217/pgs-2022-0015
摘要
Objective: To assess whether the risk of anti-tuberculosis drug-induced hepatotoxicity (ATDH) might be influenced by heme oxygenase-1 (HMOX1) and hemopexin (HPX) gene polymorphisms. Methods: A dynamic anti-tuberculosis treatment cohort was constructed, and the 1:4 matched nested case-control study was analysed. Eight single-nucleotide polymorphisms (SNPs) of the two genes were selected for genotyping and Bonferroni correction was performed to correct for multiple comparison. Results: Overall, 7.8% of patients developed ATDH. SNP rs1807714 in the HMOX1 gene had decreased effects on the risk of moderate and severe hepatotoxicity under the dominant and additive models, and hepatocellular injury under the additive model. SNP rs2682099 in the HPX gene had increased effects on the risk of moderate and severe hepatotoxicity under the recessive model. However, these associations disappeared after Bonferroni correction. Conclusion:HMOX1 and HPX gene polymorphisms might not be associated with susceptibility to ATDH in the Chinese population.
科研通智能强力驱动
Strongly Powered by AbleSci AI