A genome-wide association, polygenic risk score and sex study on opioid use disorder treatment outcomes

Abstract Opioid use disorder continues to be a health concern with a high rate of opioid related deaths occurring worldwide. Medication Assisted Treatments (MAT) have been shown to reduce opioid withdrawal, cravings and opioid use, however variability exists in individual’s treatment outcomes. Sex-s...

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Main Authors: Alannah McEvoy, Caroul Chawar, Amel Lamri, Jacqueline Hudson, Luciano Minuzzi, David C. Marsh, Lehana Thabane, Andrew D. Paterson, Zainab Samaan
Format: Article
Language:English
Published: Nature Portfolio 2023-12-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-023-49605-0
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author Alannah McEvoy
Caroul Chawar
Amel Lamri
Jacqueline Hudson
Luciano Minuzzi
David C. Marsh
Lehana Thabane
Andrew D. Paterson
Zainab Samaan
author_facet Alannah McEvoy
Caroul Chawar
Amel Lamri
Jacqueline Hudson
Luciano Minuzzi
David C. Marsh
Lehana Thabane
Andrew D. Paterson
Zainab Samaan
author_sort Alannah McEvoy
collection DOAJ
description Abstract Opioid use disorder continues to be a health concern with a high rate of opioid related deaths occurring worldwide. Medication Assisted Treatments (MAT) have been shown to reduce opioid withdrawal, cravings and opioid use, however variability exists in individual’s treatment outcomes. Sex-specific differences have been reported in opioid use patterns, polysubstance use and health and social functioning. Candidate gene studies investigating methadone dose as an outcome have identified several candidate genes and only five genome-wide associations studies have been conducted for MAT outcomes. This study aimed to identify genetic variants associated with MAT outcomes through genome-wide association study (GWAS) and test the association between genetic variants previously associated with methadone dose through a polygenic risk score (PRS). Study outcomes include: continued opioid use, relapse, methadone dose and opioid overdose. No genome-wide significance SNPs or sex-specific results were identified. The PRS identified statistically significant results (p < 0.05) for the outcome of methadone dose (R2 = 3.45 × 10–3). No other PRS was statistically significant. This study provides evidence for association between a PRS and methadone dose. More research on the PRS to increase the variance explained is needed before it can be used as a tool to help identify a suitable methadone dose within this population.
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spelling doaj.art-67ad56d376fb4475a75f2b513a7e85d62023-12-17T12:18:18ZengNature PortfolioScientific Reports2045-23222023-12-011311910.1038/s41598-023-49605-0A genome-wide association, polygenic risk score and sex study on opioid use disorder treatment outcomesAlannah McEvoy0Caroul Chawar1Amel Lamri2Jacqueline Hudson3Luciano Minuzzi4David C. Marsh5Lehana Thabane6Andrew D. Paterson7Zainab Samaan8Department of Psychiatry and Behavioural Neurosciences, McMaster UniversityDepartment of Psychiatry and Behavioural Neurosciences, McMaster UniversityDepartment of Medicine, McMaster UniversityDepartment of Psychiatry and Behavioural Neurosciences, McMaster UniversityDepartment of Psychiatry and Behavioural Neurosciences, McMaster UniversityNOSM UniversityDepartment of Health Research MethodProgram in Genetics and Genome Biology, The Hospital for Sick ChildrenDepartment of Psychiatry and Behavioural Neurosciences, McMaster UniversityAbstract Opioid use disorder continues to be a health concern with a high rate of opioid related deaths occurring worldwide. Medication Assisted Treatments (MAT) have been shown to reduce opioid withdrawal, cravings and opioid use, however variability exists in individual’s treatment outcomes. Sex-specific differences have been reported in opioid use patterns, polysubstance use and health and social functioning. Candidate gene studies investigating methadone dose as an outcome have identified several candidate genes and only five genome-wide associations studies have been conducted for MAT outcomes. This study aimed to identify genetic variants associated with MAT outcomes through genome-wide association study (GWAS) and test the association between genetic variants previously associated with methadone dose through a polygenic risk score (PRS). Study outcomes include: continued opioid use, relapse, methadone dose and opioid overdose. No genome-wide significance SNPs or sex-specific results were identified. The PRS identified statistically significant results (p < 0.05) for the outcome of methadone dose (R2 = 3.45 × 10–3). No other PRS was statistically significant. This study provides evidence for association between a PRS and methadone dose. More research on the PRS to increase the variance explained is needed before it can be used as a tool to help identify a suitable methadone dose within this population.https://doi.org/10.1038/s41598-023-49605-0
spellingShingle Alannah McEvoy
Caroul Chawar
Amel Lamri
Jacqueline Hudson
Luciano Minuzzi
David C. Marsh
Lehana Thabane
Andrew D. Paterson
Zainab Samaan
A genome-wide association, polygenic risk score and sex study on opioid use disorder treatment outcomes
Scientific Reports
title A genome-wide association, polygenic risk score and sex study on opioid use disorder treatment outcomes
title_full A genome-wide association, polygenic risk score and sex study on opioid use disorder treatment outcomes
title_fullStr A genome-wide association, polygenic risk score and sex study on opioid use disorder treatment outcomes
title_full_unstemmed A genome-wide association, polygenic risk score and sex study on opioid use disorder treatment outcomes
title_short A genome-wide association, polygenic risk score and sex study on opioid use disorder treatment outcomes
title_sort genome wide association polygenic risk score and sex study on opioid use disorder treatment outcomes
url https://doi.org/10.1038/s41598-023-49605-0
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