Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10961996 | Tuberculosis | 2015 | 7 Pages |
Abstract
This study investigated the association between genetic variants in two hepatic uptake transporter genes (SLCO1B1 and SLC10A1) and the risk of anti-tuberculosis drug-induced hepatotoxicity (ATDH) in a Chinese cohort. The frequencies and distributions of single nucleotide polymorphisms (SNPs) and haplotypes of these genes were compared among 89 incident ATDH cases and 356 matched ATDH-free controls using a multivariate conditional logistic regression analysis. After correction for potential confounding factors, significant differences were found in polymorphism of rs4149014 under an addictive model (PÂ =Â 0.008) and a recessive model (PÂ =Â 0.016). The result of haplotype analysis suggested that patients carrying at least one SLCO1B1*15 haplotype had a higher risk of ATDH (odds ratio (OR)Â =Â 1.74, 95% confidence intervals (CI): 1.04-2.90, PÂ =Â 0.034) in comparison with those carrying SLCO1B1*1a or SLCO1B1*1b haplotypes. These findings indicate that genetic variants of SLCO1B1 are associated with the development of ATDH in Chinese population.
Related Topics
Life Sciences
Immunology and Microbiology
Applied Microbiology and Biotechnology
Authors
Ru Chen, Jing Wang, Shaowen Tang, Yuan Zhang, Xiaozhen Lv, Shanshan Wu, Yinyin Xia, Peiyuan Deng, Yu Ma, Dehua Tu, Dafang Chen, Siyan Zhan,