Skip to main content

Research Repository

Advanced Search

Genome-wide analysis of 53,400 people with irritable bowel syndrome highlights shared genetic pathways with mood and anxiety disorders

Eijsbouts, Chris; Zheng, Tenghao; Kennedy, Nicholas A.; Bonfiglio, Ferdinando; Anderson, Carl A.; Moutsianas, Loukas; Holliday, Joanne; Shi, Jingchunzi; Shringarpure, Suyash; 23andMe Research Team; Voda, Alexandru-Ioan; The Bellygenes Initiative; Farrugia, Gianrico; Franke, Andre; Hübenthal, Matthias; Abecasis, Gonçalo; Zawistowski, Matthew; Skogholt, Anne Heidi; Ness-Jensen, Eivind; Hveem, Kristian; Esko, Tõnu; Teder-Laving, Maris; Zhernakova, Alexandra; Camilleri, Michael; Boeckxstaens, Guy; Whorwell, Peter J.; Spiller, Robin; McVean, Gil; D’Amato, Mauro; Jostins, Luke; Parkes, Miles

Genome-wide analysis of 53,400 people with irritable bowel syndrome highlights shared genetic pathways with mood and anxiety disorders Thumbnail


Authors

Chris Eijsbouts

Tenghao Zheng

Nicholas A. Kennedy

Ferdinando Bonfiglio

Carl A. Anderson

Loukas Moutsianas

Joanne Holliday

Jingchunzi Shi

Suyash Shringarpure

23andMe Research Team

Alexandru-Ioan Voda

The Bellygenes Initiative

Gianrico Farrugia

Andre Franke

Matthias Hübenthal

Gonçalo Abecasis

Matthew Zawistowski

Anne Heidi Skogholt

Eivind Ness-Jensen

Kristian Hveem

Tõnu Esko

Maris Teder-Laving

Alexandra Zhernakova

Michael Camilleri

Guy Boeckxstaens

Peter J. Whorwell

Gil McVean

Mauro D’Amato

Luke Jostins

Miles Parkes



Abstract

Irritable 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.

Citation

Eijsbouts, C., Zheng, T., Kennedy, N. A., Bonfiglio, F., Anderson, C. A., Moutsianas, L., Holliday, J., Shi, J., Shringarpure, S., 23andMe Research Team, Voda, A.-I., The Bellygenes Initiative, Farrugia, G., Franke, A., Hübenthal, M., Abecasis, G., Zawistowski, M., Skogholt, A. H., Ness-Jensen, E., Hveem, K., …Parkes, M. (2021). Genome-wide analysis of 53,400 people with irritable bowel syndrome highlights shared genetic pathways with mood and anxiety disorders. Nature Genetics, 53(11), 1543-1552. https://doi.org/10.1038/s41588-021-00950-8

Journal Article Type Article
Acceptance Date Sep 8, 2021
Online Publication Date Nov 5, 2021
Publication Date Nov 5, 2021
Deposit Date Jan 30, 2022
Publicly Available Date Feb 1, 2022
Journal Nature Genetics
Print ISSN 1061-4036
Electronic ISSN 1546-1718
Publisher Nature Publishing Group
Peer Reviewed Peer Reviewed
Volume 53
Issue 11
Pages 1543-1552
DOI https://doi.org/10.1038/s41588-021-00950-8
Keywords Genetics
Public URL https://nottingham-repository.worktribe.com/output/7356143
Publisher URL https://www.nature.com/articles/s41588-021-00950-8