Genetic variability of CYP2D6, CYP3A4 and CYP3A5 among the Egyptian population

被引:8
|
作者
Mutawi, Thuraya M. [1 ]
Zedan, Mohamed M. [2 ]
Yahya, Raida S. [1 ]
Zakria, Mahmoud M. [3 ]
El-Sawi, Mamdouh R. [4 ]
Gaedigk, Andrea [5 ,6 ]
机构
[1] Mansoura Univ, Children Hosp, Dept Labs, Fac Med, Mansoura 35516, Egypt
[2] Mansoura Univ, Dept Pediat, Fac Med, Mansoura 35516, Egypt
[3] Mansoura Univ, Urol & Nephrol Ctr, Fac Sci, Mansoura 35516, Egypt
[4] Mansoura Univ, Div Physiol, Dept Zool, Fac Sci, Mansoura 35516, Egypt
[5] Univ Missouri Kansas City, Childrens Mercy Kansas City, Div Clin Pharmacol Toxicol & Therapeut Innovat, Kansas City, MO 64108 USA
[6] Univ Missouri Kansas City, Sch Med, Kansas City, MO 64108 USA
关键词
genotype; phenotype Egyptian population; PHARMACOGENETICS IMPLEMENTATION CONSORTIUM; HUMAN CYTOCHROME-P450 2D6; POOR METABOLIZERS; CPIC GUIDELINE; CYP3A4-ASTERISK-22; POLYMORPHISMS; ALLELES; DUPLICATION; PHENOTYPE; VARIANTS;
D O I
10.2217/pgs-2020-0140
中图分类号
R9 [药学];
学科分类号
1007 ;
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.
引用
收藏
页码:323 / 334
页数:12
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