CYP3A5
CYP2D6型
阿拉伯语
遗传学
等位基因
生物
CYP3A4型
人口
塔克曼
等位基因频率
多态性(计算机科学)
基因
医学
聚合酶链反应
细胞色素P450
基因型
环境卫生
内分泌学
哲学
新陈代谢
语言学
作者
Thuraya M Mutawi,Mohamed M Zedan,Raida S. Yahya,Mahmoud M Zakria,Mamdouh R. El-Sawi,Andrea Gaedigk
出处
期刊:Pharmacogenomics
[Future Medicine]
日期:2021-04-01
卷期号:22 (6): 323-334
被引量:6
标识
DOI:10.2217/pgs-2020-0140
摘要
Aim: This study investigated major allelic variants of CYP2D6, CYP3A4 and CYP3A5 in Egyptians, an Arabic population for which there is little information regarding these important pharmacogenes. Patients & methods:CYP2D6*2, *4, *5, *10, *41 and gene copy number variation, as well as CYP3A4*22 and CYP3A5*3 were determined with commercially available TaqMan assays in 145 healthy study participants. Results: The CYP2D6 alleles identified suggest that the prevalence of poor metabolizers is low as none were found among the 145 subjects investigated. The frequency for CYP3A5 nonexpressers was 74.5% and the CYP3A4*22 allele frequency was low at 2.0%. Conclusion: These preliminary findings indicate that pharmacogene variation in Egyptians is different from those of other Middle Eastern/Arabic populations and warrants further investigation.
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