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巴基斯坦六个主要民族 CYP2C9 基因多态性频率的变化。

Variations in the frequencies of polymorphisms in the CYP2C9 gene in six major ethnicities of Pakistan.

机构信息

Department of Basic Medical Sciences, Shifa College of Pharmaceutical Sciences, Shifa Tameer-E-Millat University, Sector H-8, Islamabad, 44000, Pakistan.

Overseas Pakistanis Foundation Boys College, Sector H-8, Islamabad, Pakistan.

出版信息

Sci Rep. 2020 Nov 9;10(1):19370. doi: 10.1038/s41598-020-76366-x.

DOI:10.1038/s41598-020-76366-x
PMID:33168919
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7652876/
Abstract

Genetic variation in cytochrome P450 (CYP) 2C9 is known to cause significant inter-individual differences in drug response and adverse effects. The frequencies of CYP2C92 and CYP2C93, both of which are responsible for the low activity of the enzyme, are not known in the Pakistani population. Therefore, we screened various ethnic groups residing in Pakistan for these polymorphisms. A total of 467 healthy human volunteers were recruited from six major ethnicities of Pakistan after written informed consent. Our results indicate that about 20% of the Pakistani population has a genotype containing at least one low activity allele. Ethnic Punjabi and Pathan populations had the highest frequencies of wild type genotypes while Urdu, Seraiki, and Sindhi populations showed higher rates of both low activity genotypes. The Baloch population showed the highest rates of low activity genotypes with less than 50% of the samples showing wild type genotypes, suggesting that more than half of the Baloch population possesses low activity genotypes. The frequencies found in various ethnic groups in Pakistan were comparable with ethnicities in the South Asian region except for the Baloch population. These results suggest that pharmacogenetics screening for low activity genotypes may be a helpful tool for clinicians while prescribing medications metabolized by CYP2C9.

摘要

细胞色素 P450(CYP)2C9 的遗传变异导致药物反应和不良反应的个体间存在显著差异。在巴基斯坦人群中,CYP2C92 和 CYP2C93 的频率(这两种变异均导致酶活性降低)尚不清楚。因此,我们对居住在巴基斯坦的各种族人群进行了这些多态性的筛查。在书面知情同意后,我们从巴基斯坦的 6 个主要民族中招募了 467 名健康志愿者。结果表明,约 20%的巴基斯坦人群至少有一种低活性等位基因的基因型。旁遮普族和普什图族人群的野生型基因型频率最高,而乌尔都语、塞雷基语和信德语人群的低活性基因型频率较高。俾路支族人群的低活性基因型频率最高,不到 50%的样本显示野生型基因型,提示俾路支族人群中超过一半的人携带低活性基因型。在巴基斯坦各民族中发现的频率与南亚地区的民族相似,但俾路支族人群除外。这些结果表明,在为 CYP2C9 代谢的药物开处方时,低活性基因型的药物遗传学筛查可能是临床医生的有用工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5de/7652876/ca23cf993ae1/41598_2020_76366_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5de/7652876/ca23cf993ae1/41598_2020_76366_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5de/7652876/ca23cf993ae1/41598_2020_76366_Fig1_HTML.jpg

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