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

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. W...

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Autores principales: Eijsbouts, Chris, Zheng, Tenghao, Kennedy, Nicholas A., Bonfiglio, Ferdinando, Anderson, Carl A., Moutsianas, Loukas, Holliday, Joanne, Shi, Jingchunzi, Shringarpure, Suyash, Voda, Alexandru-Ioan, 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8571093/
https://www.ncbi.nlm.nih.gov/pubmed/34741163
http://dx.doi.org/10.1038/s41588-021-00950-8
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author Eijsbouts, Chris
Zheng, Tenghao
Kennedy, Nicholas A.
Bonfiglio, Ferdinando
Anderson, Carl A.
Moutsianas, Loukas
Holliday, Joanne
Shi, Jingchunzi
Shringarpure, Suyash
Voda, Alexandru-Ioan
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
author_facet Eijsbouts, Chris
Zheng, Tenghao
Kennedy, Nicholas A.
Bonfiglio, Ferdinando
Anderson, Carl A.
Moutsianas, Loukas
Holliday, Joanne
Shi, Jingchunzi
Shringarpure, Suyash
Voda, Alexandru-Ioan
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
author_sort Eijsbouts, Chris
collection PubMed
description 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 (r(g) > 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.
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spelling pubmed-85710932021-11-23 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 Voda, Alexandru-Ioan 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 Nat Genet Article 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 (r(g) > 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. Nature Publishing Group US 2021-11-05 2021 /pmc/articles/PMC8571093/ /pubmed/34741163 http://dx.doi.org/10.1038/s41588-021-00950-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Eijsbouts, Chris
Zheng, Tenghao
Kennedy, Nicholas A.
Bonfiglio, Ferdinando
Anderson, Carl A.
Moutsianas, Loukas
Holliday, Joanne
Shi, Jingchunzi
Shringarpure, Suyash
Voda, Alexandru-Ioan
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
title Genome-wide analysis of 53,400 people with irritable bowel syndrome highlights shared genetic pathways with mood and anxiety disorders
title_full Genome-wide analysis of 53,400 people with irritable bowel syndrome highlights shared genetic pathways with mood and anxiety disorders
title_fullStr Genome-wide analysis of 53,400 people with irritable bowel syndrome highlights shared genetic pathways with mood and anxiety disorders
title_full_unstemmed Genome-wide analysis of 53,400 people with irritable bowel syndrome highlights shared genetic pathways with mood and anxiety disorders
title_short Genome-wide analysis of 53,400 people with irritable bowel syndrome highlights shared genetic pathways with mood and anxiety disorders
title_sort genome-wide analysis of 53,400 people with irritable bowel syndrome highlights shared genetic pathways with mood and anxiety disorders
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8571093/
https://www.ncbi.nlm.nih.gov/pubmed/34741163
http://dx.doi.org/10.1038/s41588-021-00950-8
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