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Drug–drug–gene interactions and adverse drug reactions

The economic and health burden caused by adverse drug reactions has increased dramatically in the last few years. This is likely to be mediated by increasing polypharmacy, which increases the likelihood for drug–drug interactions. Tools utilized by healthcare practitioners to flag potential adverse...

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Detalles Bibliográficos
Autores principales: Malki, Mustafa Adnan, Pearson, Ewan Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7253354/
https://www.ncbi.nlm.nih.gov/pubmed/31792369
http://dx.doi.org/10.1038/s41397-019-0122-0
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author Malki, Mustafa Adnan
Pearson, Ewan Robert
author_facet Malki, Mustafa Adnan
Pearson, Ewan Robert
author_sort Malki, Mustafa Adnan
collection PubMed
description The economic and health burden caused by adverse drug reactions has increased dramatically in the last few years. This is likely to be mediated by increasing polypharmacy, which increases the likelihood for drug–drug interactions. Tools utilized by healthcare practitioners to flag potential adverse drug reactions secondary to drug–drug interactions ignore individual genetic variation, which has the potential to markedly alter the severity of these interactions. To date there have been limited published studies on impact of genetic variation on drug–drug interactions. In this review, we establish a detailed classification for pharmacokinetic drug–drug–gene interactions, and give examples from the literature that support this approach. The increasing availability of real-world drug outcome data linked to genetic bioresources is likely to enable the discovery of previously unrecognized, clinically important drug–drug–gene interactions.
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spelling pubmed-72533542020-06-05 Drug–drug–gene interactions and adverse drug reactions Malki, Mustafa Adnan Pearson, Ewan Robert Pharmacogenomics J Review Article The economic and health burden caused by adverse drug reactions has increased dramatically in the last few years. This is likely to be mediated by increasing polypharmacy, which increases the likelihood for drug–drug interactions. Tools utilized by healthcare practitioners to flag potential adverse drug reactions secondary to drug–drug interactions ignore individual genetic variation, which has the potential to markedly alter the severity of these interactions. To date there have been limited published studies on impact of genetic variation on drug–drug interactions. In this review, we establish a detailed classification for pharmacokinetic drug–drug–gene interactions, and give examples from the literature that support this approach. The increasing availability of real-world drug outcome data linked to genetic bioresources is likely to enable the discovery of previously unrecognized, clinically important drug–drug–gene interactions. Nature Publishing Group UK 2019-12-03 2020 /pmc/articles/PMC7253354/ /pubmed/31792369 http://dx.doi.org/10.1038/s41397-019-0122-0 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Review Article
Malki, Mustafa Adnan
Pearson, Ewan Robert
Drug–drug–gene interactions and adverse drug reactions
title Drug–drug–gene interactions and adverse drug reactions
title_full Drug–drug–gene interactions and adverse drug reactions
title_fullStr Drug–drug–gene interactions and adverse drug reactions
title_full_unstemmed Drug–drug–gene interactions and adverse drug reactions
title_short Drug–drug–gene interactions and adverse drug reactions
title_sort drug–drug–gene interactions and adverse drug reactions
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7253354/
https://www.ncbi.nlm.nih.gov/pubmed/31792369
http://dx.doi.org/10.1038/s41397-019-0122-0
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