药物基因组学
基因型
遗传学
生物
CYP3A5
人口
药物遗传学
基因
医学
环境卫生
作者
Wenting Meng,Wenjie Zhang,Shuangyu Yang,Xia Dou,Yuanwei Liu,Haiyue Li,Jianfeng Liu,Tianbo Jin,Bin Li
出处
期刊:Personalized Medicine
[Future Medicine]
日期:2022-07-08
卷期号:19 (5): 403-410
标识
DOI:10.2217/pme-2021-0157
摘要
Aim: Our study aimed to screen the genotype frequencies of very important pharmacogenomic (VIP) mutations and identify their differences between Bai and other populations. Materials & methods: We selected 66 VIP variants from PharmGKB (www.pharmgkb.org/) for genotyping. χ2 test was used to identify differences in loci between these populations and FST values of Bai and the other 26 populations were analyzed. Results: Our study showed that the frequencies of SNPs of CYP3A5, ACE, PTGS2 and NAT2 differed significantly from those of the other 26 populations. At the same time, we found that some VIP variants may affect the metabolism of drugs and the genetic relationship between the Bai population and East Asian populations was found to be the closest. Conclusion: By comparing the genotype frequencies of different populations, the loci with significant differences were identified and discussed, providing a theoretical basis for individualized drug use in the Bai ethnic population.
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