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Pharmacogenetic-guided cannabis usage in the community pharmacy: evaluation of a pilot program

BACKGROUND: Pharmacists possess a skillset suited to provide evidence-based guidance to current and potential users of cannabis. Clinical pharmacogenomics research has made significant progress in defining which genetic variations are important for influencing inter-patient variability in response t...

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Autores principales: Papastergiou, John, Li, Wilson, Sterling, Carly, van den Bemt, Bart
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7819344/
https://www.ncbi.nlm.nih.gov/pubmed/33526106
http://dx.doi.org/10.1186/s42238-020-00033-1
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author Papastergiou, John
Li, Wilson
Sterling, Carly
van den Bemt, Bart
author_facet Papastergiou, John
Li, Wilson
Sterling, Carly
van den Bemt, Bart
author_sort Papastergiou, John
collection PubMed
description BACKGROUND: Pharmacists possess a skillset suited to provide evidence-based guidance to current and potential users of cannabis. Clinical pharmacogenomics research has made significant progress in defining which genetic variations are important for influencing inter-patient variability in response to cannabis. This study aims to evaluate the practicality and impact of pharmacogenetic testing in the community pharmacy to help guide in the safe use of cannabis. METHODS: The pilot program was designed as open-label, non-randomized, and observational. Two busy, urban community pharmacies, operating under the brand Shoppers Drug Mart, in Toronto, Ontario, Canada offered pharmacogenomic testing to cannabis users as part of their professional services program over a period of 2 months. Eligible patients received buccal swabs using a DNA cheek swab kit. De-identified, barcoded samples were then sent by regular mail to an off-site CLIA-certified laboratory for analysis in Mississauga, Canada. A pharmacogenetic testing platform from Lobo Genetics® was utilized for translation of participants’ DNA with respect to CYP2C9, AKT1 and COMT genetic polymorphisms. Following genomic data translation, personalized, evidence-based recommendations were generated. Pharmacists provided a cannabis pharmacogenetic consultation to patients via telephone or in-person. RESULTS: Twenty patients enrolled in the study. Pharmacogenetic screening identified 95% as having the CYP2C9*1/*1 genotype (suggesting normal THC metabolism); 35 and 25% had AKT1 genotypes suggesting intermediate risk (C/T genotype) or high risk (C/C genotype), respectively, for cannabis-induced psychosis; and 45 and 10% had COMT genotypes suggesting intermediate risk (Val/Met genotype) or high risk (Val/Val genotype), respectively for cannabis-induced neurocognitive impairment. After the pharmacogenetic consultation, 65% of patients reported an increased comfort level in choosing a specific strength/strain of cannabis for use in the future; 75% considered the consultation of high value providing information potentially vital to their health and wellbeing. CONCLUSION: Although the study did not find any CYP2C9 variants associated with highly diminished THC metabolism, most of these patients do carry genetic variants that may potentially predispose them to the development of psychosis and memory impairment. Similar initiatives can potentially improve patient safety and empower individuals to make informed decisions about cannabis use and possible complications.
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spelling pubmed-78193442021-01-25 Pharmacogenetic-guided cannabis usage in the community pharmacy: evaluation of a pilot program Papastergiou, John Li, Wilson Sterling, Carly van den Bemt, Bart J Cannabis Res Brief Research Report BACKGROUND: Pharmacists possess a skillset suited to provide evidence-based guidance to current and potential users of cannabis. Clinical pharmacogenomics research has made significant progress in defining which genetic variations are important for influencing inter-patient variability in response to cannabis. This study aims to evaluate the practicality and impact of pharmacogenetic testing in the community pharmacy to help guide in the safe use of cannabis. METHODS: The pilot program was designed as open-label, non-randomized, and observational. Two busy, urban community pharmacies, operating under the brand Shoppers Drug Mart, in Toronto, Ontario, Canada offered pharmacogenomic testing to cannabis users as part of their professional services program over a period of 2 months. Eligible patients received buccal swabs using a DNA cheek swab kit. De-identified, barcoded samples were then sent by regular mail to an off-site CLIA-certified laboratory for analysis in Mississauga, Canada. A pharmacogenetic testing platform from Lobo Genetics® was utilized for translation of participants’ DNA with respect to CYP2C9, AKT1 and COMT genetic polymorphisms. Following genomic data translation, personalized, evidence-based recommendations were generated. Pharmacists provided a cannabis pharmacogenetic consultation to patients via telephone or in-person. RESULTS: Twenty patients enrolled in the study. Pharmacogenetic screening identified 95% as having the CYP2C9*1/*1 genotype (suggesting normal THC metabolism); 35 and 25% had AKT1 genotypes suggesting intermediate risk (C/T genotype) or high risk (C/C genotype), respectively, for cannabis-induced psychosis; and 45 and 10% had COMT genotypes suggesting intermediate risk (Val/Met genotype) or high risk (Val/Val genotype), respectively for cannabis-induced neurocognitive impairment. After the pharmacogenetic consultation, 65% of patients reported an increased comfort level in choosing a specific strength/strain of cannabis for use in the future; 75% considered the consultation of high value providing information potentially vital to their health and wellbeing. CONCLUSION: Although the study did not find any CYP2C9 variants associated with highly diminished THC metabolism, most of these patients do carry genetic variants that may potentially predispose them to the development of psychosis and memory impairment. Similar initiatives can potentially improve patient safety and empower individuals to make informed decisions about cannabis use and possible complications. BioMed Central 2020-09-01 /pmc/articles/PMC7819344/ /pubmed/33526106 http://dx.doi.org/10.1186/s42238-020-00033-1 Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Brief Research Report
Papastergiou, John
Li, Wilson
Sterling, Carly
van den Bemt, Bart
Pharmacogenetic-guided cannabis usage in the community pharmacy: evaluation of a pilot program
title Pharmacogenetic-guided cannabis usage in the community pharmacy: evaluation of a pilot program
title_full Pharmacogenetic-guided cannabis usage in the community pharmacy: evaluation of a pilot program
title_fullStr Pharmacogenetic-guided cannabis usage in the community pharmacy: evaluation of a pilot program
title_full_unstemmed Pharmacogenetic-guided cannabis usage in the community pharmacy: evaluation of a pilot program
title_short Pharmacogenetic-guided cannabis usage in the community pharmacy: evaluation of a pilot program
title_sort pharmacogenetic-guided cannabis usage in the community pharmacy: evaluation of a pilot program
topic Brief Research Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7819344/
https://www.ncbi.nlm.nih.gov/pubmed/33526106
http://dx.doi.org/10.1186/s42238-020-00033-1
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