| Literature DB >> 25498879 |
Ru Chen1, Jing Wang1, Shaowen Tang2, Yuan Zhang3, Xiaozhen Lv4, Shanshan Wu1, Yinyin Xia5, Peiyuan Deng6, Yu Ma7, Dehua Tu8, Dafang Chen1, Siyan Zhan9.
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 (P = 0.008) and a recessive model (P = 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) = 1.74, 95% confidence intervals (CI): 1.04-2.90, P = 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.Entities:
Keywords: Anti-tuberculosis drug; Drug transporter; Hepatotoxicity
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Year: 2014 PMID: 25498879 DOI: 10.1016/j.tube.2014.11.004
Source DB: PubMed Journal: Tuberculosis (Edinb) ISSN: 1472-9792 Impact factor: 3.131