GWAS-identified genetic variants associated with medication-assisted treatment outcomes in patients with opioid use disorder: a systematic review and meta-analysis protocol.


Journal

Systematic reviews
ISSN: 2046-4053
Titre abrégé: Syst Rev
Pays: England
ID NLM: 101580575

Informations de publication

Date de publication:
01 09 2020
Historique:
received: 20 04 2020
accepted: 21 08 2020
entrez: 3 9 2020
pubmed: 3 9 2020
medline: 22 6 2021
Statut: epublish

Résumé

The burden of opioid use disorder (OUD) has been increasing in North America. Administration of medication-assisted treatments (MATs) for OUD on an individual-dose basis has been shown to affect patient responses to treatment, proving to be, on occasion, dangerous. A genetic basis has been identified for some MAT responses in a candidate gene context, but consensus has not been reached for any genome-wide significant associations. This systematic review aims to identify and assess any genetic variants associated with MAT patient outcomes at genome-wide significance. The databases searched by the authors will be: MEDLINE, Web of Science, EMBASE, CINAHL and Pre-CINAHL, GWAS Catalog, GWAS Central, and NIH Database of Genotypes and Phenotypes. A title and abstract screening, full-text screening, data extraction, and quality assessment will be completed in duplicate for each study via Covidence. Treatment outcomes of interest include continued opioid use or abstinence during treatment or at follow-up, time to relapse, treatment retention rates, opioid overdose, other substance use, comorbid psychiatric disorders, risk taking behaviors, MAT plasma concentrations, and mortality rates. Analysis methods applied, if appropriate, will include random effects meta-analysis with pooled odds ratios for all outcomes. Subgroup analyses will also be implemented, when possible. This systematic review can hopefully inform the direction of future research, aiding in the development of a safer and more patient-centered treatment. It will be able to highlight genome-wide significant variants that are replicable and associated with MAT patient outcomes. This systematic review protocol has been registered with the International Prospective Register of Systematic Reviews (PROSPERO) (registration ID CRD42020169121).

Sections du résumé

BACKGROUND
The burden of opioid use disorder (OUD) has been increasing in North America. Administration of medication-assisted treatments (MATs) for OUD on an individual-dose basis has been shown to affect patient responses to treatment, proving to be, on occasion, dangerous. A genetic basis has been identified for some MAT responses in a candidate gene context, but consensus has not been reached for any genome-wide significant associations. This systematic review aims to identify and assess any genetic variants associated with MAT patient outcomes at genome-wide significance.
METHODS
The databases searched by the authors will be: MEDLINE, Web of Science, EMBASE, CINAHL and Pre-CINAHL, GWAS Catalog, GWAS Central, and NIH Database of Genotypes and Phenotypes. A title and abstract screening, full-text screening, data extraction, and quality assessment will be completed in duplicate for each study via Covidence. Treatment outcomes of interest include continued opioid use or abstinence during treatment or at follow-up, time to relapse, treatment retention rates, opioid overdose, other substance use, comorbid psychiatric disorders, risk taking behaviors, MAT plasma concentrations, and mortality rates. Analysis methods applied, if appropriate, will include random effects meta-analysis with pooled odds ratios for all outcomes. Subgroup analyses will also be implemented, when possible.
DISCUSSION
This systematic review can hopefully inform the direction of future research, aiding in the development of a safer and more patient-centered treatment. It will be able to highlight genome-wide significant variants that are replicable and associated with MAT patient outcomes.
SYSTEMATIC REVIEW REGISTRATION
This systematic review protocol has been registered with the International Prospective Register of Systematic Reviews (PROSPERO) (registration ID CRD42020169121).

Identifiants

pubmed: 32873330
doi: 10.1186/s13643-020-01461-z
pii: 10.1186/s13643-020-01461-z
pmc: PMC7466496
doi:

Substances chimiques

Analgesics, Opioid 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

200

Subventions

Organisme : CIHR
ID : PJT-156306
Pays : Canada

Références

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pubmed: 8042602
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pubmed: 22253303
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pubmed: 20418051
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pubmed: 21185693
Curr Psychiatry Rev. 2014 May;10(2):156-167
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BMJ. 2017 Apr 26;357:j1550
pubmed: 28446428

Auteurs

Caroul Chawar (C)

Neuroscience Graduate Program, McMaster University, Hamilton, ON, Canada.
Department of Psychiatry and Behavioural Neurosciences, St. Joseph's Healthcare Hamilton, Hamilton, ON, Canada.

Alannah Hillmer (A)

Neuroscience Graduate Program, McMaster University, Hamilton, ON, Canada.
Department of Psychiatry and Behavioural Neurosciences, St. Joseph's Healthcare Hamilton, Hamilton, ON, Canada.

Stephanie Sanger (S)

Health Sciences Library, McMaster University, Hamilton, ON, Canada.

Alessia D'Elia (A)

Neuroscience Graduate Program, McMaster University, Hamilton, ON, Canada.
Department of Psychiatry and Behavioural Neurosciences, St. Joseph's Healthcare Hamilton, Hamilton, ON, Canada.

Balpreet Panesar (B)

Neuroscience Graduate Program, McMaster University, Hamilton, ON, Canada.
Department of Psychiatry and Behavioural Neurosciences, St. Joseph's Healthcare Hamilton, Hamilton, ON, Canada.

Lucy Guan (L)

Department of Psychiatry and Behavioural Neurosciences, St. Joseph's Healthcare Hamilton, Hamilton, ON, Canada.
Health Sciences Program, McMaster University, Hamilton, ON, Canada.

Dave Xiaofei Xie (DX)

Department of Psychiatry and Behavioural Neurosciences, St. Joseph's Healthcare Hamilton, Hamilton, ON, Canada.
Health Sciences Program, McMaster University, Hamilton, ON, Canada.

Nandini Bansal (N)

Department of Psychiatry and Behavioural Neurosciences, St. Joseph's Healthcare Hamilton, Hamilton, ON, Canada.
Health Sciences Program, McMaster University, Hamilton, ON, Canada.

Aamna Abdullah (A)

Department of Psychiatry and Behavioural Neurosciences, St. Joseph's Healthcare Hamilton, Hamilton, ON, Canada.
Health Sciences Program, McMaster University, Hamilton, ON, Canada.

Flavio Kapczinski (F)

Department of Psychiatry and Behavioural Neurosciences, St. Joseph's Healthcare Hamilton, Hamilton, ON, Canada.

Guillaume Pare (G)

Population Health Research Institute, Hamilton, ON, Canada.
Department of Health Research Method, Evidence, and Impact, McMaster University, Hamilton, ON, Canada.

Lehana Thabane (L)

Population Health Research Institute, Hamilton, ON, Canada.
Department of Health Research Method, Evidence, and Impact, McMaster University, Hamilton, ON, Canada.
Father Sean O'Sullivan Research Centre, St. Joseph's Healthcare Hamilton, Hamilton, ON, Canada.

Zainab Samaan (Z)

Department of Psychiatry and Behavioural Neurosciences, St. Joseph's Healthcare Hamilton, Hamilton, ON, Canada. samaanz@mcmaster.ca.

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