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dc.date.accessioned2024-02-19T16:33:17Z
dc.date.available2024-02-19T16:33:17Z
dc.date.created2023-06-05T17:15:34Z
dc.date.issued2023
dc.identifier.citationCheng, Weiqiu Parker, Nadine Karadag, Naz Koch, Elise Hindley, Guy Frederick Lanyon Icick, Romain Shadrin, Alexey O'Connell, Kevin Sean Bjella, Thomas Bahrami, Shahram Rahman, Zillur Woldeyohannes, Markos Tesfaye Jaholkowski, Piotr Pawel Rødevand, Linn Holen, Børge Lagerberg, Trine Vik Steen, Nils Eiel Djurovic, Srdjan Dale, Anders M Frei, Oleksandr Smeland, Olav Bjerkehagen Andreassen, Ole . The relationship between cannabis use, schizophrenia, and bipolar disorder: a genetically informed study. The Lancet Psychiatry. 2023, 10(6), 441-451
dc.identifier.urihttp://hdl.handle.net/10852/108289
dc.description.abstractBackground The 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). Methods We 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. Findings Psychotic 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. Interpretation A 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.
dc.languageEN
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.titleThe relationship between cannabis use, schizophrenia, and bipolar disorder: a genetically informed study
dc.title.alternativeENEngelskEnglishThe relationship between cannabis use, schizophrenia, and bipolar disorder: a genetically informed study
dc.typeJournal article
dc.creator.authorCheng, Weiqiu
dc.creator.authorParker, Nadine
dc.creator.authorKaradag, Naz
dc.creator.authorKoch, Elise
dc.creator.authorHindley, Guy Frederick Lanyon
dc.creator.authorIcick, Romain
dc.creator.authorShadrin, Alexey
dc.creator.authorO'Connell, Kevin Sean
dc.creator.authorBjella, Thomas
dc.creator.authorBahrami, Shahram
dc.creator.authorRahman, Zillur
dc.creator.authorWoldeyohannes, Markos Tesfaye
dc.creator.authorJaholkowski, Piotr Pawel
dc.creator.authorRødevand, Linn
dc.creator.authorHolen, Børge
dc.creator.authorLagerberg, Trine Vik
dc.creator.authorSteen, Nils Eiel
dc.creator.authorDjurovic, Srdjan
dc.creator.authorDale, Anders M
dc.creator.authorFrei, Oleksandr
dc.creator.authorSmeland, Olav Bjerkehagen
dc.creator.authorAndreassen, Ole
cristin.unitcode185,53,10,70
cristin.unitnameSenter for presisjonspsykiatri
cristin.ispublishedtrue
cristin.fulltextpostprint
cristin.qualitycode2
dc.identifier.cristin2152039
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=The Lancet Psychiatry&rft.volume=10&rft.spage=441&rft.date=2023
dc.identifier.jtitleThe Lancet Psychiatry
dc.identifier.volume10
dc.identifier.issue6
dc.identifier.startpage441
dc.identifier.endpage451
dc.identifier.doihttps://doi.org/10.1016/S2215-0366(23)00143-8
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.source.issn2215-0374
dc.type.versionAcceptedVersion
dc.relation.projectSIGMA2/NS9666S
dc.relation.projectNFR/223273
dc.relation.projectNFR/223273


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