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中国拉祜族人群中非常重要的药物基因组学变异分析。

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

作者信息

Cheng Yujing, Li Qi, Yang Xin, Ding Heng, Chen Wanlu, Dai Run, Zhang Chan

机构信息

Department of Blood Transfusion, First People's Hospital of Yunnan, Kunming City, 650021, Yunnan Province, People's Republic of China.

Blood Station of Honghe State Center, Honghe Prefecture City, 661100, Yunnan Province, People's Republic of China.

出版信息

Pharmgenomics Pers Med. 2021 Oct 1;14:1275-1289. doi: 10.2147/PGPM.S324410. eCollection 2021.

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.

摘要

背景

显然,基因多态性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无报道。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Agena MassARRAY单核苷酸多态性(SNP)基因分型技术检测拉祜族人群中81个药物基因组学基因的VIP突变,并将其基因型频率与其他11个主要群体进行比较。采用卡方检验来确定这些群体之间的不同位点。最后,分析了拉祜族与其他11个群体的遗传结构和成对Fst值。

结果

我们发现,拉祜族不同药物基因内的等位基因频率分布与其他群体存在显著差异。此外,成对F统计量(Fst)值和遗传结构表明,拉祜族人群中的变异在基因上也大多与中国北京的汉族(CHB)和日本东京的日本人群体(JPT)相关。

结论

本研究将为安全用药提供理论依据,并有助于在拉祜族人群中建立适当的个体化治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9de9/8493477/a82da4d26fe9/PGPM-14-1275-g0001.jpg

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