Analysis of Very Important Pharmacogenomics Variants in the Chinese Lahu Population.

Pharmacogenomics and Personalized Medicine Pub Date : 2021-10-01 eCollection Date: 2021-01-01 DOI:10.2147/PGPM.S324410
Yujing Cheng, Qi Li, Xin Yang, Heng Ding, Wanlu Chen, Run Dai, Chan Zhang
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引用次数: 1

Abstract

Background: Genetic polymorphism, obviously, has a potential clinical role in determining differences in drug efficacy; however, there are no reports about the pharmacogenomic information of the Lahu population. Therefore, our research aimed to screen the genotypic frequencies of the very important pharmacogenomics (VIP) mutations and determined the differences between Lahu and the other 11 populations.

Methods: Agena MassARRAY (AgenaMassARRAY) single nucleotide polymorphism (SNP) genotyping technique was used to detect 81 VIP mutations of pharmacogenomics genes in Lahu, and their genotypic frequencies were compared with the other major 11 populations. Chi-square tests were used to identify different loci among these populations. Finally, the genetic structure and pairwise Fst values of Lahu and the other 11 populations were analyzed.

Results: We found that the distribution of allele frequencies within different pharmacogenes in Lahu showed significantly different with other populations. Additionally, the pairwise F-statistics (Fst) values and genetic structure revealed the variants in the Lahu population as well were mostly related to the Han Chinese in Beijing, China (CHB) and the Japanese population in Tokyo, Japan (JPT) genetically.

Conclusion: This study will provide a theoretical basis for safe drug use and help to establish the appropriate individualized treatment strategies in the Lahu population.

Abstract Image

Abstract Image

中国拉祜族人群重要药物基因组变异分析。
背景:基因多态性显然在决定药物疗效差异方面具有潜在的临床作用;然而,关于拉祜族人群的药物基因组学信息尚未见报道。因此,我们的研究旨在筛选非常重要的药物基因组学(VIP)突变的基因型频率,并确定拉祜族与其他11个群体之间的差异。方法:采用AgenaMassARRAY (AgenaMassARRAY)单核苷酸多态性(SNP)基因分型技术检测拉祜族81个药物基因组学基因VIP突变,并与其他11个主要人群进行基因分型频率比较。卡方检验用于在这些群体中确定不同的位点。最后,对拉祜族和其他11个群体的遗传结构和Fst值进行了分析。结果:拉祜族不同药原基因的等位基因频率分布与其他人群有显著差异。此外,Fst值和遗传结构表明,拉祜族人群的变异也与中国北京汉族(CHB)和日本东京人群(JPT)的遗传关系密切。结论:本研究将为拉祜族人群安全用药提供理论依据,并有助于制定适当的个性化治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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