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Genetic polymorphisms of drug-metabolizing phase I enzymes CYP2E1, CYP2A6 and CYP3A5 in South Indian population

机译:药物代谢I期酶CYP2E1,CYP2A6和CYP3A5在南印度人群中的遗传多态性

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CYP2E1, CYP2A6 and CYP3A5 enzymes belong to phase I group of drug-metabolizing enzymes, which are involved in the metabolism of various compounds and xenobiotics. Presence of polymorphisms in the genes coding for these enzymes results in interindividual variations in drug metabolism, therapeutic response and susceptibility towards various diseases. The frequencies of these variants in genes differ considerably between ethnic groups. This study was carried out to estimate the allele and genotype frequencies of common variants in CYP2E1, CYP2A6 and CYP3A5 in South Indian population. Six hundred and fifty-two unrelated healthy volunteers of South Indian origin (Andhra Pradesh, Karnataka, Kerala and Tamil Nadu) were included in this study. Polymerase chain reaction-restriction fragment length polymorphism, allele-specific PCR, real-time PCR, SNaPshot and gene sequencing methods were used for the identification of gene polymorphisms. The frequencies of CYP2E1*1B, CYP2E1*5B and CYP2E1*6 alleles in South Indian population were 14.3, 1.3 and 22.4%, respectively. The frequencies of CYP2A6*2, CYP2A6*4A and CYP2A6*5 alleles were found to be 1, 8.9 and 0.7%, respectively. The distribution of CYP3A5*3 allele was 63.5%. There were no variant alleles of CYP3A5*2, CYP3A5*4 and CYP3A5*6 in South Indian population. The frequencies of CYP2E1, CYP2A6 and CYP3A5 in the South Indian population are distinct from Caucasians, Chinese, Japanese, African Americans and other compared populations. This is the first study conducted in the South Indian population with a larger sample size. The findings of our study provide the basic genetic information for further pharmacogenomic investigations in the population.
机译:CYP2E1,CYP2A6和CYP3A5酶属于药物代谢酶的I期组,它们参与各种化合物和异生物素的代谢。在编码这些酶的基因中多态性的存在导致药物代谢,治疗反应和对各种疾病的敏感性之间的个体差异。这些变异基因的频率在不同种族之间有很大差异。进行这项研究来估计南印度人CYP2E1,CYP2A6和CYP3A5常见变异的等位基因和基因型频率。这项研究包括来自印度南部的542名无亲属健康志愿者(安得拉邦,卡纳塔克邦,喀拉拉邦和泰米尔纳德邦)。聚合酶链反应限制片段长度多态性,等位基因特异性PCR,实时荧光定量PCR,SNaPshot和基因测序方法用于鉴定基因多态性。 CYP2E1 * 1B,CYP2E1 * 5B和CYP2E1 * 6等位基因在南印度人群中的频率分别为14.3%,1.3%和22.4%。 CYP2A6 * 2,CYP2A6 * 4A和CYP2A6 * 5等位基因的频率分别为1,8.9%和0.7%。 CYP3A5 * 3等位基因分布为63.5%。在南印度人群中没有CYP3A5 * 2,CYP3A5 * 4和CYP3A5 * 6的变异等位基因。 CYP2E1,CYP2A6和CYP3A5在南印度人口中的频率不同于白种人,华人,日本人,非裔美国人和其他比较的人口。这是在南印度人口中进行的第一项样本量较大的研究。我们的研究结果为人群中进一步的药物基因组学研究提供了基本的遗传信息。

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