Genetic Polymorphism of Drug Metabolic Gene CYPs, VKORC1, NAT2, DPYD and CHST3 of Five Ethnic Minorities in Heilongjiang Province, Northeast China.

Pharmacogenomics and Personalized Medicine Pub Date : 2021-11-30 eCollection Date: 2021-01-01 DOI:10.2147/PGPM.S339854
Tingting Zhang, Qiuyan Li, Bonan Dong, Xiao Liang, Mansha Jia, Jing Bai, Jingcui Yu, Songbin Fu
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引用次数: 1

Abstract

Introduction: Genetic variability in genes encoding drug-metabolizing enzymes may contribute to the heterogeneity of drug responses in different populations. Extensive research in pharmacogenomics in major populations around the world provides us with a great deal of information about drug-related genetic polymorphisms.

Objective: The purpose of this study was to detect the genetic variation of drug-metabolism-related genes in the five ethnic minorities Daur, Hezhen, Ewenki, Mongolian and Manchu in China, and to analyze the distribution differences among ethnic groups.

Methods: We genotyped 32 SNPs of drug metabolism genes in 882 healthy Chinese volunteers from five ethnic groups. The genotype frequency and allele frequency of the five ethnic groups were calculated, and the different variants among the five ethnic groups were compared by chi-square test. Genetic parameters were analyzed using Popgene software. The genetic structure of five ethnic minorities was analyzed by principal component analysis, and compared with 26 populations.

Results: We found that SNPs of genes related to drug metabolism existed diversity in different populations. Among them, rs8192766 and rs9419082 in CYP2E1 showed statistical differences between Daur and Manchu, and NAT2 rs1801280 showed statistical differences between Hezhen and Mongolian. In addition, the five populations we studied had the smallest differences with EAS populations. There was haplotype diversity in CHST3, VKORC1, CYP1A2 and CYP2E1 genes in the five ethnic minorities, and these haplotype polymorphisms were related to the use of corresponding drug doses. Cluster analysis shows that the five ethnic minorities in Heilongjiang Province are clustered together with the EAS populations.

Conclusion: These results suggest that understanding the diversity of drug-related genetic markers is critical for individualized drug gene therapy programs in ethnic minorities in China as well as in populations highly mixed with these ethnic groups.

Abstract Image

Abstract Image

黑龙江省5个少数民族药物代谢基因CYPs、VKORC1、NAT2、DPYD和CHST3的遗传多态性
基因编码药物代谢酶的遗传变异可能导致不同人群药物反应的异质性。药物基因组学在世界主要人群中的广泛研究为我们提供了大量与药物相关的遗传多态性信息。目的:检测达斡尔族、赫哲族、鄂温克族、蒙古族和满族5个少数民族药物代谢相关基因的遗传变异,并分析其在各民族间的分布差异。方法:对来自5个民族的882名中国健康志愿者的32个药物代谢基因snp进行基因分型。计算5个民族的基因型频率和等位基因频率,并采用卡方检验比较5个民族的不同变异。采用Popgene软件对遗传参数进行分析。采用主成分分析法对5个少数民族的遗传结构进行了分析,并与26个居群进行了比较。结果:药物代谢相关基因snp在不同人群中存在多样性。其中CYP2E1基因rs8192766、rs9419082在达斡尔族与满族之间存在统计学差异,NAT2基因rs1801280在赫哲族与蒙族之间存在统计学差异。此外,我们研究的五个种群与EAS种群的差异最小。5个少数民族CHST3、VKORC1、CYP1A2和CYP2E1基因存在单倍型多样性,且这些单倍型多态性与使用相应的药物剂量有关。聚类分析表明,黑龙江省五大少数民族与东亚地区人口聚在一起。结论:这些结果表明,了解药物相关遗传标记的多样性对于中国少数民族以及这些少数民族高度混杂人群的个体化药物基因治疗方案至关重要。
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