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Polymorphisms in drug transporter genes (ABCB1, SLCO1B1 and ABCC2) and hepatitis induced by antituberculosis drugs

机译:抗结核药物诱导的药物转运蛋白基因(ABCB1,SLCO1B1和ABCC2)和肝炎的多态性

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摘要

Unusual drug accumulation is a common mechanism underlying serious drug-induced liver injury. Polymorphisms in three drug transporter genes (ABCB1, SLCO1B1 and ABCC2) may be risk markers for hepatitis induced by the unusual accumulation of anti-tuberculosis drugs (ATDs). We therefore investigated whether polymorphisms and haplotypes of these genes are associated with ATD-induced hepatitis by comparing the frequencies and distributions of single nucleotide polymorphisms and haplotypes of these three drug transporter genes among 67 patients with ATD-induced hepatitis and 159 patients tolerant to ATDs using a multivariate logistic regression analysis. We found that the frequencies of polymorphisms and haplotypes of ABCB1, SLCO1B1 and ABCC2 were similar in patients with ATD-induced hepatitis and ATD-tolerant controls. The present results suggest that these drug transporters do not play important roles in the pathogenesis of ATD-induced hepatitis in Korean patients.
机译:异常的药物蓄积是引起严重药物诱发的肝损伤的常见机制。三种药物转运蛋白基因(ABCB1,SLCO1B1和ABCC2)的多态性可能是由抗结核药物(ATD)异常积累引起的肝炎的危险标志。因此,我们通过比较67例ATD诱发的肝炎患者和159例耐受ATD的患者中这三种药物转运蛋白基因的单核苷酸多态性和单倍型的频率和分布,调查了这些基因的多态性和单倍型是否与ATD诱发的肝炎相关。多元逻辑回归分析。我们发现,在ATD诱发的肝炎患者和ATD耐受的患者中,ABCB1,SLCO1B1和ABCC2的多态性和单倍型频率相似。目前的结果表明,这些药物转运蛋白在韩国患者的ATD诱发的肝炎的发病机理中不发挥重要作用。

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