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CYP2C19 genotype-guided antiplatelet therapy: promises and pitfalls

Pharmacogenetic variants can alter the mechanism of action (pharmacodynamic gene variants) or kinetic processes such as absorption, distribution, metabolism and elimination (pharmacokinetic gene variants). Many initial successes in precision medicine occurred in the context of genes encoding the cyt...

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Autores principales: Ellithi, Moataz, Baye, Jordan, Wilke, Russell A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Future Medicine Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7444625/
https://www.ncbi.nlm.nih.gov/pubmed/32723143
http://dx.doi.org/10.2217/pgs-2020-0046
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author Ellithi, Moataz
Baye, Jordan
Wilke, Russell A
author_facet Ellithi, Moataz
Baye, Jordan
Wilke, Russell A
author_sort Ellithi, Moataz
collection PubMed
description Pharmacogenetic variants can alter the mechanism of action (pharmacodynamic gene variants) or kinetic processes such as absorption, distribution, metabolism and elimination (pharmacokinetic gene variants). Many initial successes in precision medicine occurred in the context of genes encoding the cytochromes P450 (CYP enzymes). CYP2C19 activates the antiplatelet drug clopidogrel, and polymorphisms in the CYP2C19 gene are known to alter the outcome for patients taking clopidogrel in the context of cardiovascular disease. CYP2C19 loss-of-function alleles are specifically associated with increased risk for coronary stent thrombosis and major adverse cardiovascular events in patients taking clopidogrel following percutaneous coronary intervention. We explore successes and challenges encountered as the clinical and scientific communities advance CYP2C19 genotyping in the context of routine patient care.
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spelling pubmed-74446252020-08-28 CYP2C19 genotype-guided antiplatelet therapy: promises and pitfalls Ellithi, Moataz Baye, Jordan Wilke, Russell A Pharmacogenomics Review Pharmacogenetic variants can alter the mechanism of action (pharmacodynamic gene variants) or kinetic processes such as absorption, distribution, metabolism and elimination (pharmacokinetic gene variants). Many initial successes in precision medicine occurred in the context of genes encoding the cytochromes P450 (CYP enzymes). CYP2C19 activates the antiplatelet drug clopidogrel, and polymorphisms in the CYP2C19 gene are known to alter the outcome for patients taking clopidogrel in the context of cardiovascular disease. CYP2C19 loss-of-function alleles are specifically associated with increased risk for coronary stent thrombosis and major adverse cardiovascular events in patients taking clopidogrel following percutaneous coronary intervention. We explore successes and challenges encountered as the clinical and scientific communities advance CYP2C19 genotyping in the context of routine patient care. Future Medicine Ltd 2020-07-29 2020-08 /pmc/articles/PMC7444625/ /pubmed/32723143 http://dx.doi.org/10.2217/pgs-2020-0046 Text en © Russell Wilke This work is licensed under the Attribution-NonCommercial-NoDerivatives 4.0 Unported License (http://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Review
Ellithi, Moataz
Baye, Jordan
Wilke, Russell A
CYP2C19 genotype-guided antiplatelet therapy: promises and pitfalls
title CYP2C19 genotype-guided antiplatelet therapy: promises and pitfalls
title_full CYP2C19 genotype-guided antiplatelet therapy: promises and pitfalls
title_fullStr CYP2C19 genotype-guided antiplatelet therapy: promises and pitfalls
title_full_unstemmed CYP2C19 genotype-guided antiplatelet therapy: promises and pitfalls
title_short CYP2C19 genotype-guided antiplatelet therapy: promises and pitfalls
title_sort cyp2c19 genotype-guided antiplatelet therapy: promises and pitfalls
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7444625/
https://www.ncbi.nlm.nih.gov/pubmed/32723143
http://dx.doi.org/10.2217/pgs-2020-0046
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