Guo Jinping, Zhou Wenqian, Ma Xiaoya, Li Yujie, Zhang Huan, Wei Jie, Du Shuli, Jin Tianbo
Key Laboratory of Resource Biology and Biotechnology in Western China (Northwest University), School of Life Sciences, Ministry of Education, Northwest University, #229 North TaiBai Road, Xi'an, Shaanxi, 710069, China.
College of Life Science, Northwest University, Xi'an, 710127, China.
Biochem Genet. 2024 Jun 8. doi: 10.1007/s10528-024-10748-y.
Genetic polymorphisms of very important pharmacogenes (VIP) are a significant factor contributing to inter-individual variability in drug therapy. The purpose of this study was to identify significantly different loci in the Yi population and to enrich their pharmacogenomic information. 54 VIP variants were selected from the Pharmacogenomics Knowledge Base (PharmGKB) and genotyped in 200 Yi individuals. Then, we compared their genotype distribution between the Yi population and the other 26 populations using the χ test. Compared with the other 26 populations, the genotype frequencies of 4 single nucleotide polymorphisms (SNPs), rs2108622 (CYP4F2), rs1065852 (CYP2D6), rs2070676 (CYP2E1), and rs4291 (ACE), had significant differences in the Yi population. For example, the TT genotype frequency of rs2108622 (8.1%) was higher than that of African populations, and the AA genotype frequency of rs1065852 (27.3%) was higher than that of other populations except East Asians. We also found that the Yi populations differed the least from East Asians and the most from Africans. Furthermore, the differences in these variants might be related to the effectiveness and toxicity risk of using warfarin, iloperidone, cisplatin cyclophosphamide, and other drugs in the Yi population. Our data complement the pharmacogenomic information of the Yi population and provide theoretical guidance for their personalized treatment.
非常重要的药物代谢基因(VIP)的遗传多态性是导致药物治疗个体差异的重要因素。本研究的目的是确定彝族人群中存在显著差异的基因座,并丰富其药物基因组学信息。从药物基因组学知识库(PharmGKB)中选取了54个VIP变异位点,并对200名彝族个体进行基因分型。然后,我们使用χ检验比较了彝族人群与其他26个群体之间的基因型分布。与其他26个群体相比,彝族人群中4个单核苷酸多态性(SNP),即rs2108622(CYP4F2)、rs1065852(CYP2D6)、rs2070676(CYP2E1)和rs4291(ACE)的基因型频率存在显著差异。例如,rs2108622的TT基因型频率(8.1%)高于非洲人群,rs1065852的AA基因型频率(27.3%)高于除东亚人群以外的其他人群。我们还发现彝族人群与东亚人群差异最小,与非洲人群差异最大。此外,这些变异的差异可能与彝族人群使用华法林、伊潘立酮、顺铂环磷酰胺等药物的有效性和毒性风险有关。我们的数据补充了彝族人群的药物基因组学信息,并为其个性化治疗提供了理论指导。