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Depression and 24 gastrointestinal diseases: a Mendelian randomization study
The causality of the association between depression and gastrointestinal diseases is undetermined. We conducted Mendelian randomization (MR) analyses to systematically explore the associations of depression with 24 gastrointestinal diseases. Independent genetic variants associated with depression at...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10160129/ https://www.ncbi.nlm.nih.gov/pubmed/37142593 http://dx.doi.org/10.1038/s41398-023-02459-6 |
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author | Ruan, Xixian Chen, Jie Sun, Yuhao Zhang, Yao Zhao, Jianhui Wang, Xiaoyan Li, Xue Yuan, Shuai Larsson, Susanna C. |
author_facet | Ruan, Xixian Chen, Jie Sun, Yuhao Zhang, Yao Zhao, Jianhui Wang, Xiaoyan Li, Xue Yuan, Shuai Larsson, Susanna C. |
author_sort | Ruan, Xixian |
collection | PubMed |
description | The causality of the association between depression and gastrointestinal diseases is undetermined. We conducted Mendelian randomization (MR) analyses to systematically explore the associations of depression with 24 gastrointestinal diseases. Independent genetic variants associated with depression at the genome-wide significance level were selected as instrumental variables. Genetic associations with 24 gastrointestinal diseases were obtained from the UK Biobank study, the FinnGen study, and large consortia. Multivariable MR analysis was conducted to explore the mediation effects of body mass index, cigarette smoking, and type 2 diabetes. After multiple-testing corrections, genetic liability to depression was associated with an increased risk of irritable bowel syndrome, non-alcohol fatty liver disease, alcoholic liver disease, gastroesophageal reflux, chronic pancreatitis, duodenal ulcer, chronic gastritis, gastric ulcer, diverticular disease, cholelithiasis, acute pancreatitis, and ulcerative colitis. For the causal effect of genetic liability to depression on non-alcoholic fatty liver disease, a substantial proportion was mediated by body mass index. Genetic predisposition to smoking initiation mediated half of effect of depression on acute pancreatitis. This MR study suggests that depression may play a causal role in many gastrointestinal diseases. |
format | Online Article Text |
id | pubmed-10160129 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-101601292023-05-06 Depression and 24 gastrointestinal diseases: a Mendelian randomization study Ruan, Xixian Chen, Jie Sun, Yuhao Zhang, Yao Zhao, Jianhui Wang, Xiaoyan Li, Xue Yuan, Shuai Larsson, Susanna C. Transl Psychiatry Article The causality of the association between depression and gastrointestinal diseases is undetermined. We conducted Mendelian randomization (MR) analyses to systematically explore the associations of depression with 24 gastrointestinal diseases. Independent genetic variants associated with depression at the genome-wide significance level were selected as instrumental variables. Genetic associations with 24 gastrointestinal diseases were obtained from the UK Biobank study, the FinnGen study, and large consortia. Multivariable MR analysis was conducted to explore the mediation effects of body mass index, cigarette smoking, and type 2 diabetes. After multiple-testing corrections, genetic liability to depression was associated with an increased risk of irritable bowel syndrome, non-alcohol fatty liver disease, alcoholic liver disease, gastroesophageal reflux, chronic pancreatitis, duodenal ulcer, chronic gastritis, gastric ulcer, diverticular disease, cholelithiasis, acute pancreatitis, and ulcerative colitis. For the causal effect of genetic liability to depression on non-alcoholic fatty liver disease, a substantial proportion was mediated by body mass index. Genetic predisposition to smoking initiation mediated half of effect of depression on acute pancreatitis. This MR study suggests that depression may play a causal role in many gastrointestinal diseases. Nature Publishing Group UK 2023-05-04 /pmc/articles/PMC10160129/ /pubmed/37142593 http://dx.doi.org/10.1038/s41398-023-02459-6 Text en © The Author(s) 2023 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 Ruan, Xixian Chen, Jie Sun, Yuhao Zhang, Yao Zhao, Jianhui Wang, Xiaoyan Li, Xue Yuan, Shuai Larsson, Susanna C. Depression and 24 gastrointestinal diseases: a Mendelian randomization study |
title | Depression and 24 gastrointestinal diseases: a Mendelian randomization study |
title_full | Depression and 24 gastrointestinal diseases: a Mendelian randomization study |
title_fullStr | Depression and 24 gastrointestinal diseases: a Mendelian randomization study |
title_full_unstemmed | Depression and 24 gastrointestinal diseases: a Mendelian randomization study |
title_short | Depression and 24 gastrointestinal diseases: a Mendelian randomization study |
title_sort | depression and 24 gastrointestinal diseases: a mendelian randomization study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10160129/ https://www.ncbi.nlm.nih.gov/pubmed/37142593 http://dx.doi.org/10.1038/s41398-023-02459-6 |
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