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Use of Pharmacogenetic Drugs by the Dutch Population

INTRODUCTION: The Dutch Pharmacogenetics Working Group (DPWG) indicated a list of actionable genotypes that affect patients’ response to more 50 drugs; these drugs which show variable effects based on patients’ genetic traits were named as pharmacogenetics (PGX) drugs. Preemptive genetic testing bef...

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Autores principales: Alshabeeb, Mohammad A., Deneer, Vera H. M., Khan, Amjad, Asselbergs, Folkert W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6614185/
https://www.ncbi.nlm.nih.gov/pubmed/31312209
http://dx.doi.org/10.3389/fgene.2019.00567
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author Alshabeeb, Mohammad A.
Deneer, Vera H. M.
Khan, Amjad
Asselbergs, Folkert W.
author_facet Alshabeeb, Mohammad A.
Deneer, Vera H. M.
Khan, Amjad
Asselbergs, Folkert W.
author_sort Alshabeeb, Mohammad A.
collection PubMed
description INTRODUCTION: The Dutch Pharmacogenetics Working Group (DPWG) indicated a list of actionable genotypes that affect patients’ response to more 50 drugs; these drugs which show variable effects based on patients’ genetic traits were named as pharmacogenetics (PGX) drugs. Preemptive genetic testing before using these drugs may protect certain patients from serious adverse reactions and could help in avoiding treatment failures. The objectives of this study include identifying the rate of PGX drug usage among Dutch population, estimating the level of users who carry the actionable genotypes and determining the main genes involved in drug’s effect variability. METHODS: Usage of PGX drugs over 2011–2017 by the insured population (an average of 11.4 million) in outpatient clinics in Netherlands was obtained from the publically available GIP databank. The data of 45 drugs were analyzed and their interactions with selected pharmacogenes were estimated. Frequency of actionable genotypes of 249 Dutch parents was obtained from the public database: Genome of Netherlands (GoNL), to identify the pattern of genetic characteristics of Dutch population. RESULTS: Over a 7 year period, 51.3 million exposures of patients to PGX drugs were reported with an average of 5.3 exposures per each drug user. One quarterof the exposures (12.4 million) are predicted to be experienced by individuals with actionable genotypes (risky exposures). Up to 60% of the risky exposures (around 7.5 million) were related to drugs metabolized by CYP2D6. SLCO1B1, and CYP2C19 were also identified among the top genes affecting response of drugs users (involved in about 22 and 12.4% of the risky exposures, respectively). Cardiovascular medications were the top prescribed PGX drug class (43%), followed by gastroenterology (29%) and psychiatry/neurology medications (15%). Women use more PGX drugs than men (55.8 vs. 44.2%, respectively) with the majority (84%) of users in both sexes are above 45 years. CONCLUSION: PGX drugs are commonly used in Netherlands. Preemptive panel testing for CYP2D6, SLCO1B1, and CYP2C19 only could be useful to predict 95% of vulnerable patients’ exposures to PGX drugs. Future studies to assess the economic impact of preemptive panel testing on patients of older age are suggested.
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spelling pubmed-66141852019-07-16 Use of Pharmacogenetic Drugs by the Dutch Population Alshabeeb, Mohammad A. Deneer, Vera H. M. Khan, Amjad Asselbergs, Folkert W. Front Genet Genetics INTRODUCTION: The Dutch Pharmacogenetics Working Group (DPWG) indicated a list of actionable genotypes that affect patients’ response to more 50 drugs; these drugs which show variable effects based on patients’ genetic traits were named as pharmacogenetics (PGX) drugs. Preemptive genetic testing before using these drugs may protect certain patients from serious adverse reactions and could help in avoiding treatment failures. The objectives of this study include identifying the rate of PGX drug usage among Dutch population, estimating the level of users who carry the actionable genotypes and determining the main genes involved in drug’s effect variability. METHODS: Usage of PGX drugs over 2011–2017 by the insured population (an average of 11.4 million) in outpatient clinics in Netherlands was obtained from the publically available GIP databank. The data of 45 drugs were analyzed and their interactions with selected pharmacogenes were estimated. Frequency of actionable genotypes of 249 Dutch parents was obtained from the public database: Genome of Netherlands (GoNL), to identify the pattern of genetic characteristics of Dutch population. RESULTS: Over a 7 year period, 51.3 million exposures of patients to PGX drugs were reported with an average of 5.3 exposures per each drug user. One quarterof the exposures (12.4 million) are predicted to be experienced by individuals with actionable genotypes (risky exposures). Up to 60% of the risky exposures (around 7.5 million) were related to drugs metabolized by CYP2D6. SLCO1B1, and CYP2C19 were also identified among the top genes affecting response of drugs users (involved in about 22 and 12.4% of the risky exposures, respectively). Cardiovascular medications were the top prescribed PGX drug class (43%), followed by gastroenterology (29%) and psychiatry/neurology medications (15%). Women use more PGX drugs than men (55.8 vs. 44.2%, respectively) with the majority (84%) of users in both sexes are above 45 years. CONCLUSION: PGX drugs are commonly used in Netherlands. Preemptive panel testing for CYP2D6, SLCO1B1, and CYP2C19 only could be useful to predict 95% of vulnerable patients’ exposures to PGX drugs. Future studies to assess the economic impact of preemptive panel testing on patients of older age are suggested. Frontiers Media S.A. 2019-07-02 /pmc/articles/PMC6614185/ /pubmed/31312209 http://dx.doi.org/10.3389/fgene.2019.00567 Text en Copyright © 2019 Alshabeeb, Deneer, Khan and Asselbergs. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Alshabeeb, Mohammad A.
Deneer, Vera H. M.
Khan, Amjad
Asselbergs, Folkert W.
Use of Pharmacogenetic Drugs by the Dutch Population
title Use of Pharmacogenetic Drugs by the Dutch Population
title_full Use of Pharmacogenetic Drugs by the Dutch Population
title_fullStr Use of Pharmacogenetic Drugs by the Dutch Population
title_full_unstemmed Use of Pharmacogenetic Drugs by the Dutch Population
title_short Use of Pharmacogenetic Drugs by the Dutch Population
title_sort use of pharmacogenetic drugs by the dutch population
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6614185/
https://www.ncbi.nlm.nih.gov/pubmed/31312209
http://dx.doi.org/10.3389/fgene.2019.00567
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