Pharmacogenetic biomarkers as tools for improved drug therapy; emphasis on the cytochrome P450 system

被引:37
作者
Ingelman-Sundberg, Magnus [1 ]
Sim, Sarah C. [1 ]
机构
[1] Karolinska Inst, Dept Physiol & Pharmacol, Pharmacogenet Sect, SE-17177 Stockholm, Sweden
基金
瑞典研究理事会;
关键词
Adverse drug reactions; Drug metabolism; Clopidogrel; CYP2C19; CYP2D6; CYP2C19-ASTERISK-17; ALLELE; DEBRISOQUINE HYDROXYLATION; ULTRARAPID METABOLISM; BREAST-CANCER; CYP2D6; ANTIDEPRESSANTS; GENOTYPE; CYP2C19; VARIANT; LOCUS;
D O I
10.1016/j.bbrc.2010.02.162
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Important interindividual differences in drug pharmacokinetics cause absence of drug response or adverse drug reactions in significant fractions of the populations. The identification of the major enzymes participating, and the elucidation of the genetic basis for this variation in particular among cytochromes P450, provide tools for a personalized medicine treatment, which can make drug therapy much more effective at a lower cost. Much of the pioneering work linking drug metabolizing phenotype to genetic polymorphism among the P450 enzymes has been carried out at Karolinska Institutet. In this review we give a background and description of this work as well as the important implications for future medicine. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:90 / 94
页数:5
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