Evidence map›Paper›PMID 37494403›Full record

ArticlePloS one2023

Genetics of cannabis use in opioid use disorder: A genome-wide association and polygenic risk score study.

Alannah Hillmer, Caroul Chawar, Amel Lamri, Jacqueline Hudson, Flavio Kapczinski, Luciano Minuzzi, David C Marsh, Lehana Thabane, Andrew D Paterson, Zainab Samaan

Abstract read
In one paragraph

Article in PloS one, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Alannah HillmerDepartment of Psychiatry and Behavioural Neurosciences, McMaster University, Hamilton, ON, Canada.ORCID 0000-0002-5535-7432
Caroul ChawarDepartment of Psychiatry and Behavioural Neurosciences, McMaster University, Hamilton, ON, Canada.ORCID 0000-0001-8935-5454
Amel LamriDepartment of Medicine, McMaster University, Hamilton, ON, Canada.
Jacqueline HudsonDepartment of Psychiatry and Behavioural Neurosciences, McMaster University, Hamilton, ON, Canada.
Flavio KapczinskiMcMaster University, Hamilton, ON, Canada.
Luciano MinuzziDepartment of Psychiatry and Behavioural Neurosciences, McMaster University, Hamilton, ON, Canada.ORCID 0000-0001-7532-1851
David C MarshNOSM University, Sudbury, ON, Canada.
Lehana ThabaneDepartment of Health Research Method, Evidence & Impact, Hamilton, ON, Canada.
Andrew D PatersonProgram in Genetics and Genome Biology, The Hospital for Sick Children, Divisions of Biostatistics and Epidemiology, Dalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada.
Zainab SamaanDepartment of Psychiatry and Behavioural Neurosciences, McMaster University, Hamilton, ON, Canada.ORCID 0000-0002-5974-9361

Funding

CIHR PJT-156306
6 · The paper itself

Abstract

backgroundIndividuals with an Opioid Use Disorder (OUD) have increased rates of cannabis use in comparison to the general population. Research on the short- and long-term impacts of cannabis use in OUD patients has been inconclusive. A genetic component may contribute to cannabis cravings.

aimsIdentify genetic variants associated with cannabis use through Genome-wide Association Study (GWAS) methods and investigate a Polygenic Risk Score (PRS). In addition, we aim to identify any sex differences in effect size for genetic variants reaching or nearing genome-wide significance in the GWAS.

methodsThe study outcomes of interest were: regular cannabis use (yes/no) (n = 2616), heaviness of cannabis use (n = 1293) and cannabis cravings (n = 836). Logistic and linear regressions were preformed, respectively, to test the association between genetic variants and each outcome, regular cannabis use and heaviness of cannabis use. GWAS summary statistics from a recent large meta-GWAS investigating cannabis use disorder were used to conduct PRS's. Findings are limited to a European ancestry sample.

resultsNo genome-wide significant associations were found. Rs1813412 (chromosome 17) for regular cannabis use and rs62378502 (chromosome 5) for heaviness of cannabis use were approaching genome-wide significance. Both these SNPs were nominally significant (p<0.05) within males and females, however sex did not modify the association. The PRS identified statistically significant association with cannabis cravings. The variance explained by all PRSs were less than 1.02x10-2.

conclusionThis study provides promising results in understanding the genetic contribution to cannabis use in individuals living with OUD.

Indexed as

CannabisOpioid-Related DisordersFemaleGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansMaleMultifactorial InheritanceRisk Factors

Identifiers

PMID37494403
PMCPMC10370765

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.