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抗氧化途径中的遗传变异:结核病患者肝毒性的危险因素。

Genetic variants in antioxidant pathway: risk factors for hepatotoxicity in tuberculosis patients.

机构信息

Department of Pharmacotherapeutics, Nagasaki University Graduate School of Biomedical Sciences, 1-14 Bunkyo-machi, Nagasaki 852-8521, Japan.

出版信息

Tuberculosis (Edinb). 2012 May;92(3):253-9. doi: 10.1016/j.tube.2011.12.004. Epub 2012 Feb 15.

Abstract

Tuberculosis (TB) treatment can cause serious sequelae including adverse effects such as anti-TB drug-induced hepatotoxicity (ATDH). We performed a candidate gene-based association study between single nucleotide polymorphisms (SNPs) in 10 genes in the antioxidant pathway and ATDH susceptibility. The subjects comprised 100 Japanese patients with pulmonary TB who received a treatment regimen including isoniazid and rifampicin. Out of them, 18 patients had ATDH. Thirty-four tag SNPs in 10 genes were analyzed by PCR-restriction fragment length polymorphism or PCR-direct DNA sequencing. The frequencies of alleles and genotypes between patients with and without ATDH were compared in three different genetic models. Statistical analyses revealed that a C/C genotype at rs11080344 in NOS2A, a C/C genotype at rs2070401 in BACH1, and a G/A or A/A genotype at rs4720833 in MAFK independently conferred ATDH susceptibility. Remarkably, the association of the latter two tag SNPs with ATDH susceptibility was highly statistically significant (P = 0.0006) with an odds ratio of 9.730. This study is the first report to demonstrate that NOS2A, BACH1, and MAFK appear to be genetic determinants of ATDH in Japanese patients with TB. Furthermore, a combination of BACH1 and MAFK polymorphisms may be useful as new biomarkers to identify high-risk Japanese TB patients for ATDH.

摘要

结核病 (TB) 治疗可能会导致严重的后遗症,包括抗结核药物引起的肝毒性 (ATDH) 等不良反应。我们进行了一项基于候选基因的关联研究,探讨了抗氧化途径中 10 个基因的单核苷酸多态性 (SNP) 与 ATDH 易感性之间的关系。研究对象包括 100 名接受异烟肼和利福平治疗方案的日本肺结核患者。其中,18 名患者出现了 ATDH。通过 PCR-限制性片段长度多态性或 PCR-直接 DNA 测序分析了 10 个基因中的 34 个标记 SNP。在三种不同的遗传模型中比较了 ATDH 患者和无 ATDH 患者之间等位基因和基因型的频率。统计分析显示,NOS2A 中的 rs11080344 处的 C/C 基因型、BACH1 中的 rs2070401 处的 C/C 基因型以及 MAFK 中的 rs4720833 处的 G/A 或 A/A 基因型独立地赋予 ATDH 易感性。值得注意的是,后两个标记 SNP 与 ATDH 易感性的关联具有高度统计学意义 (P = 0.0006),其优势比为 9.730。本研究首次表明,NOS2A、BACH1 和 MAFK 似乎是日本结核病患者 ATDH 的遗传决定因素。此外,BACH1 和 MAFK 多态性的组合可能是识别日本结核病患者 ATDH 高危人群的新生物标志物。

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