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Published in: Clinical Pharmacokinetics 3/2015

01-03-2015 | Letter to the Editor

Quantitative Methods for Prediction of the Effect of Cytochrome P450 Gene Polymorphisms on Substrate Drug Exposure

Authors: Sylvain Goutelle, Michel Tod

Published in: Clinical Pharmacokinetics | Issue 3/2015

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Excerpt

We read with interest the article by Chang and colleagues who studied the influence of cytochrome P450 2C19 (CYP2C19) genetic polymorphism on citalopram and escitalopram exposure by using meta-analysis [1]. The authors state that this is the first study which provides precise estimates of the influence of CYP2C19 genotypes on (es)citalopram drug exposure, especially for heterozygous genotypes with the CYP2C19*17 gain-of-function allele. …
Literature
1.
go back to reference Chang M, Tybring G, Dahl ML, Lindh JD. Impact of cytochrome P450 2C19 polymorphisms on citalopram/escitalopram exposure: a systematic review and meta-analysis. Clin Pharmacokinet. 2014;53(9):801–11.CrossRefPubMed Chang M, Tybring G, Dahl ML, Lindh JD. Impact of cytochrome P450 2C19 polymorphisms on citalopram/escitalopram exposure: a systematic review and meta-analysis. Clin Pharmacokinet. 2014;53(9):801–11.CrossRefPubMed
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go back to reference Goutelle S, Bourguignon L, Bleyzac N, Berry J, Clavel-Grabit F, Tod M. In vivo quantitative prediction of the effect of gene polymorphisms and drug interactions on drug exposure for CYP2C19 substrates. AAPS J. 2013;15(2):415–26.CrossRefPubMedCentralPubMed Goutelle S, Bourguignon L, Bleyzac N, Berry J, Clavel-Grabit F, Tod M. In vivo quantitative prediction of the effect of gene polymorphisms and drug interactions on drug exposure for CYP2C19 substrates. AAPS J. 2013;15(2):415–26.CrossRefPubMedCentralPubMed
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go back to reference Tod M, Goutelle S, Gagnieu MC. Genotype-based quantitative prediction of drug exposure for drugs metabolized by CYP2D6. Clin Pharmacol Ther. 2011;90(4):582–7.CrossRefPubMed Tod M, Goutelle S, Gagnieu MC. Genotype-based quantitative prediction of drug exposure for drugs metabolized by CYP2D6. Clin Pharmacol Ther. 2011;90(4):582–7.CrossRefPubMed
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go back to reference Castellan AC, Tod M, Gueyffier F, Audars M, Cambriels F, Kassai B, et al. Quantitative prediction of the impact of drug interactions and genetic polymorphisms on cytochrome P450 2C9 substrate exposure. Clin Pharmacokinet. 2013;52(3):199–209.CrossRefPubMed Castellan AC, Tod M, Gueyffier F, Audars M, Cambriels F, Kassai B, et al. Quantitative prediction of the impact of drug interactions and genetic polymorphisms on cytochrome P450 2C9 substrate exposure. Clin Pharmacokinet. 2013;52(3):199–209.CrossRefPubMed
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go back to reference Weiss J, Ten Hoevel MM, Burhenne J, Walter-Sack I, Hoffmann MM, Rengelshausen J, et al. CYP2C19 genotype is a major factor contributing to the highly variable pharmacokinetics of voriconazole. J Clin Pharmacol. 2009;49(2):196–204.CrossRefPubMed Weiss J, Ten Hoevel MM, Burhenne J, Walter-Sack I, Hoffmann MM, Rengelshausen J, et al. CYP2C19 genotype is a major factor contributing to the highly variable pharmacokinetics of voriconazole. J Clin Pharmacol. 2009;49(2):196–204.CrossRefPubMed
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Metadata
Title
Quantitative Methods for Prediction of the Effect of Cytochrome P450 Gene Polymorphisms on Substrate Drug Exposure
Authors
Sylvain Goutelle
Michel Tod
Publication date
01-03-2015
Publisher
Springer International Publishing
Published in
Clinical Pharmacokinetics / Issue 3/2015
Print ISSN: 0312-5963
Electronic ISSN: 1179-1926
DOI
https://doi.org/10.1007/s40262-014-0217-3

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