Genetic Variation in Drug Transporters in Ethnic Populations (vol 84, pg, 412, 2008)

被引:40
作者
Cropp, C. D.
Yee, S. W.
Giacomini, K. M.
机构
[1] Department of Biopharmaceutical Sciences, University of California, San Francisco, San Francisco, CA
关键词
D O I
10.1038/clpt.2008.98
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Drug-metabolizing enzymes and membrane transporters work in concert to play crucial roles in drug absorption, distribution, and elimination. It is well recognized that genetic variation in drug-metabolizing enzymes contributes substantially to interindividual differences in drug response. With the notable exceptions of CYP1A1 and CYP2E1, genes encoding cytochrome P450s, which are involved in the metabolism of >80% of all drugs used in clinical practice, are highly polymorphic.1 Interethnic variation in the distribution and frequency of occurrence of variant alleles in drug-metabolizing enzymes is known to alter the rate of drug metabolism in vivo, resulting in interethnic variation in drug disposition and response. © 2008 American Society for Clinical Pharmacology and Therapeutics.
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页码:108 / 109
页数:2
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