Evidence map›Paper›PMID 37208114›Full record

ArticleThe lancet. Psychiatry2023

The relationship between cannabis use, schizophrenia, and bipolar disorder: a genetically informed study.

Weiqiu Cheng, Nadine Parker, Naz Karadag, Elise Koch, Guy Hindley, Romain Icick, Alexey Shadrin, Kevin S O'Connell, Thomas Bjella, Shahram Bahrami and 12 more

Open access · greenAbstract read
In one paragraph

Article in The lancet. Psychiatry, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 3 pooled it
12.8field-weighted citation impact, top 1% of its field
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

34 citing papers in PubMed, 3 syntheses or guidelines pooled it, 41 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Genetic overlap between treatment-resistant schizophrenia and smoking initiation.The international journal of neuropsychopharmacology · 2026
    Article
  5. Article
  6. Review
  7. Leveraging the genetics of psychiatric disorders to prioritize potential drug targets and compounds.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. 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

22 authors at 5 institutions in 5 countries.

Weiqiu ChengNORMENT, Centre for Mental Disorders Research, Division of Mental Health and Addiction, University of Oslo, Oslo, Norway.
Nadine ParkerNORMENT, Centre for Mental Disorders Research, Division of Mental Health and Addiction, University of Oslo, Oslo, Norway.
Naz KaradagNORMENT, Centre for Mental Disorders Research, Division of Mental Health and Addiction, University of Oslo, Oslo, Norway.
Elise KochNORMENT, Centre for Mental Disorders Research, Division of Mental Health and Addiction, University of Oslo, Oslo, Norway.
Guy HindleyNORMENT, Centre for Mental Disorders Research, Division of Mental Health and Addiction, University of Oslo, Oslo, Norway; Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.
Romain IcickINSERM UMR-S1144, University of Paris, Paris, France.
Alexey ShadrinNORMENT, Centre for Mental Disorders Research, Division of Mental Health and Addiction, University of Oslo, Oslo, Norway; KG Jebsen Centre for Neurodevelopmental disorders, University of Oslo, Oslo, Norway.
Kevin S O'ConnellNORMENT, Centre for Mental Disorders Research, Division of Mental Health and Addiction, University of Oslo, Oslo, Norway.
Thomas BjellaNORMENT, Centre for Mental Disorders Research, Division of Mental Health and Addiction, University of Oslo, Oslo, Norway.
Shahram BahramiNORMENT, Centre for Mental Disorders Research, Division of Mental Health and Addiction, University of Oslo, Oslo, Norway.
Zillur RahmanNORMENT, Centre for Mental Disorders Research, Division of Mental Health and Addiction, University of Oslo, Oslo, Norway.
Markos TesfayeNORMENT, Centre for Mental Disorders Research, Division of Mental Health and Addiction, University of Oslo, Oslo, Norway; Department of Psychiatry, St Paul's Hospital Millennium Medical College, Addis Ababa, Ethiopia.
Piotr JaholkowskiNORMENT, Centre for Mental Disorders Research, Division of Mental Health and Addiction, University of Oslo, Oslo, Norway.
Linn RødevandNORMENT, Centre for Mental Disorders Research, Division of Mental Health and Addiction, University of Oslo, Oslo, Norway.
Børge HolenNORMENT, Centre for Mental Disorders Research, Division of Mental Health and Addiction, University of Oslo, Oslo, Norway.
Trine Vik LagerbergNORMENT, Centre for Mental Disorders Research, Division of Mental Health and Addiction, University of Oslo, Oslo, Norway.
Nils Eiel SteenNORMENT, Centre for Mental Disorders Research, Division of Mental Health and Addiction, University of Oslo, Oslo, Norway.
Srdjan DjurovicDepartment of Medical Genetics, Oslo University Hospital, Oslo, Norway; NORMENT, Department of Clinical Science, University of Bergen, Bergen, Norway.
Anders M DaleDepartment of Psychiatry, and Department of Neurosciences, and Department of Radiology, University of California San Diego, La Jolla, CA, USA.
Oleksandr FreiNORMENT, Centre for Mental Disorders Research, Division of Mental Health and Addiction, University of Oslo, Oslo, Norway; Center for Bioinformatics, Department of Informatics, University of Oslo, Oslo, Norway.
Olav B SmelandNORMENT, Centre for Mental Disorders Research, Division of Mental Health and Addiction, University of Oslo, Oslo, Norway.
Ole A AndreassenNORMENT, Centre for Mental Disorders Research, Division of Mental Health and Addiction, University of Oslo, Oslo, Norway. Electronic address: ole.andreassen@medisin.uio.no.
University of Oslo · NOInserm · FRKing's College London · GBOslo University Hospital · NOUniversity of California, San Diego · US

Funding

Spatiotemporal Brain Imaging: Microscopic &System LevelR01EB000790 · NIBIB · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI DALE, ANDERS M · 2002 to 2015
$15.3M
Neuronal, glial and BOLD fMRI signals: From BOLD to 2-photon microscopyR01NS057198 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI DEVOR, ANNA · 2009 to 2017
$2.6M
3/7 Psychiatric Genomics Consortium: Advancing Discovery and ImpactR01MH124839 · NIMH · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI ANDREASSEN, OLE A, HUCKINS, LAURA MARIANNE · 2021 to 2025
$2.0M
NIBIB NIH HHS R01 EB000790NIMH NIH HHS R01 MH124839NINDS NIH HHS R01 NS057198
6 · The paper itself

Abstract

backgroundThe relationship between psychotic disorders and cannabis use is heavily debated. Shared underlying genetic risk is one potential explanation. We investigated the genetic association between psychotic disorders (schizophrenia and bipolar disorder) and cannabis phenotypes (lifetime cannabis use and cannabis use disorder).

methodsWe used genome-wide association summary statistics from individuals with European ancestry from the Psychiatric Genomics Consortium, UK Biobank, and International Cannabis Consortium. We estimated heritability, polygenicity, and discoverability of each phenotype. We performed genome-wide and local genetic correlations. Shared loci were identified and mapped to genes, which were tested for functional enrichment. Shared genetic liabilities to psychotic disorders and cannabis phenotypes were explored using causal analyses and polygenic scores, using the Norwegian Thematically Organized Psychosis cohort.

findingsPsychotic disorders were more heritable than cannabis phenotypes and more polygenic than cannabis use disorder. We observed positive genome-wide genetic correlations between psychotic disorders and cannabis phenotypes (range 0·22-0·35) with a mixture of positive and negative local genetic correlations. Three to 27 shared loci were identified for the psychotic disorder and cannabis phenotype pairs. Enrichment of mapped genes implicated neuronal and olfactory cells as well as drug-gene targets for nicotine, alcohol, and duloxetine. Psychotic disorders showed a causal effect on cannabis phenotypes, and lifetime cannabis use had a causal effect on bipolar disorder. Of 2181 European participants from the Norwegian Thematically Organized Psychosis cohort applied in polygenic risk score analyses, 1060 (48·6%) were females and 1121 (51·4%) were males (mean age 33·1 years [SD 11·8]). 400 participants had bipolar disorder, 697 had schizophrenia, and 1044 were healthy controls. Within this sample, polygenic scores for cannabis phenotypes predicted psychotic disorders independently and improved prediction beyond the polygenic score for the psychotic disorders.

interpretationA subgroup of individuals might have a high genetic risk of developing a psychotic disorder and using cannabis. This finding supports public health efforts to reduce cannabis use, particularly in individuals at high risk or patients with psychotic disorders. Identified shared loci and their functional implications could facilitate development of novel treatments.

fundingUS National Institutes of Health, the Research Council Norway, the South-East Regional Health Authority, Stiftelsen Kristian Gerhard Jebsen, EEA-RO-NO-2018-0535, European Union's Horizon 2020 Research and Innovation Programme, the Marie Skłodowska-Curie Actions, and University of Oslo Life Science.

Indexed as

Bipolar DisorderCannabisMarijuana AbuseSchizophreniaSubstance-Related DisordersAnimalsGenetic Predisposition to DiseaseGenome-Wide Association Study

Identifiers

PMID37208114
PMCPMC10311008
OpenAlexW4376866885

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.