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dc.contributor.authorEijsbouts, Chris
dc.contributor.authorSkogholt, Anne Heidi
dc.contributor.authorNess-Jensen, Eivind
dc.contributor.authorHveem, Kristian
dc.date.accessioned2022-03-28T11:29:47Z
dc.date.available2022-03-28T11:29:47Z
dc.date.created2022-01-07T09:55:07Z
dc.date.issued2021
dc.identifier.citationNature Genetics. 2021, 53 (11), 1543-1552.en_US
dc.identifier.issn1061-4036
dc.identifier.urihttps://hdl.handle.net/11250/2987966
dc.description.abstractIrritable bowel syndrome (IBS) results from disordered brain–gut interactions. Identifying susceptibility genes could highlight the underlying pathophysiological mechanisms. We designed a digestive health questionnaire for UK Biobank and combined identified cases with IBS with independent cohorts. We conducted a genome-wide association study with 53,400 cases and 433,201 controls and replicated significant associations in a 23andMe panel (205,252 cases and 1,384,055 controls). Our study identified and confirmed six genetic susceptibility loci for IBS. Implicated genes included NCAM1, CADM2, PHF2/FAM120A, DOCK9, CKAP2/TPTE2P3 and BAG6. The first four are associated with mood and anxiety disorders, expressed in the nervous system, or both. Mirroring this, we also found strong genome-wide correlation between the risk of IBS and anxiety, neuroticism and depression (rg > 0.5). Additional analyses suggested this arises due to shared pathogenic pathways rather than, for example, anxiety causing abdominal symptoms. Implicated mechanisms require further exploration to help understand the altered brain–gut interactions underlying IBS.en_US
dc.language.isoengen_US
dc.publisherNature Researchen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleGenome-wide analysis of 53,400 people with irritable bowel syndrome highlights shared genetic pathways with mood and anxiety disordersen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.source.pagenumber1543-1552en_US
dc.source.volume53en_US
dc.source.journalNature Geneticsen_US
dc.source.issue11en_US
dc.identifier.doi10.1038/s41588-021-00950-8
dc.identifier.cristin1976330
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2


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