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Smoking, alcohol consumption, and 24 gastrointestinal diseases: Mendelian randomization analysis

BACKGROUND: Whether the positive associations of smoking and alcohol consumption with gastrointestinal diseases are causal is uncertain. We conducted this Mendelian randomization (MR) to comprehensively examine associations of smoking and alcohol consumption with common gastrointestinal diseases. ME...

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Autores principales: Yuan, Shuai, Chen, Jie, Ruan, Xixian, Sun, Yuhao, Zhang, Ke, Wang, Xiaoyan, Li, Xue, Gill, Dipender, Burgess, Stephen, Giovannucci, Edward, Larsson, Susanna C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10017103/
https://www.ncbi.nlm.nih.gov/pubmed/36727839
http://dx.doi.org/10.7554/eLife.84051
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author Yuan, Shuai
Chen, Jie
Ruan, Xixian
Sun, Yuhao
Zhang, Ke
Wang, Xiaoyan
Li, Xue
Gill, Dipender
Burgess, Stephen
Giovannucci, Edward
Larsson, Susanna C
author_facet Yuan, Shuai
Chen, Jie
Ruan, Xixian
Sun, Yuhao
Zhang, Ke
Wang, Xiaoyan
Li, Xue
Gill, Dipender
Burgess, Stephen
Giovannucci, Edward
Larsson, Susanna C
author_sort Yuan, Shuai
collection PubMed
description BACKGROUND: Whether the positive associations of smoking and alcohol consumption with gastrointestinal diseases are causal is uncertain. We conducted this Mendelian randomization (MR) to comprehensively examine associations of smoking and alcohol consumption with common gastrointestinal diseases. METHODS: Genetic variants associated with smoking initiation and alcohol consumption at the genome-wide significance level were selected as instrumental variables. Genetic associations with 24 gastrointestinal diseases were obtained from the UK Biobank, FinnGen study, and other large consortia. Univariable and multivariable MR analyses were conducted to estimate the overall and independent MR associations after mutual adjustment for genetic liability to smoking and alcohol consumption. RESULTS: Genetic predisposition to smoking initiation was associated with increased risk of 20 of 24 gastrointestinal diseases, including 7 upper gastrointestinal diseases (gastroesophageal reflux, esophageal cancer, gastric ulcer, duodenal ulcer, acute gastritis, chronic gastritis, and gastric cancer), 4 lower gastrointestinal diseases (irritable bowel syndrome, diverticular disease, Crohn’s disease, and ulcerative colitis), 8 hepatobiliary and pancreatic diseases (non-alcoholic fatty liver disease, alcoholic liver disease, cirrhosis, liver cancer, cholecystitis, cholelithiasis, and acute and chronic pancreatitis), and acute appendicitis. Fifteen out of 20 associations persisted after adjusting for genetically predicted alcohol consumption. Genetically predicted higher alcohol consumption was associated with increased risk of duodenal ulcer, alcoholic liver disease, cirrhosis, and chronic pancreatitis; however, the association for duodenal ulcer did not remain statistically significant after adjustment for genetic predisposition to smoking initiation. CONCLUSIONS: This study provides MR evidence supporting causal associations of smoking with a broad range of gastrointestinal diseases, whereas alcohol consumption was associated with only a few gastrointestinal diseases. FUNDING: The Natural Science Fund for Distinguished Young Scholars of Zhejiang Province; National Natural Science Foundation of China; Key Project of Research and Development Plan of Hunan Province; the Swedish Heart Lung Foundation; the Swedish Research Council; the Swedish Cancer Society.
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spelling pubmed-100171032023-03-16 Smoking, alcohol consumption, and 24 gastrointestinal diseases: Mendelian randomization analysis Yuan, Shuai Chen, Jie Ruan, Xixian Sun, Yuhao Zhang, Ke Wang, Xiaoyan Li, Xue Gill, Dipender Burgess, Stephen Giovannucci, Edward Larsson, Susanna C eLife Epidemiology and Global Health BACKGROUND: Whether the positive associations of smoking and alcohol consumption with gastrointestinal diseases are causal is uncertain. We conducted this Mendelian randomization (MR) to comprehensively examine associations of smoking and alcohol consumption with common gastrointestinal diseases. METHODS: Genetic variants associated with smoking initiation and alcohol consumption at the genome-wide significance level were selected as instrumental variables. Genetic associations with 24 gastrointestinal diseases were obtained from the UK Biobank, FinnGen study, and other large consortia. Univariable and multivariable MR analyses were conducted to estimate the overall and independent MR associations after mutual adjustment for genetic liability to smoking and alcohol consumption. RESULTS: Genetic predisposition to smoking initiation was associated with increased risk of 20 of 24 gastrointestinal diseases, including 7 upper gastrointestinal diseases (gastroesophageal reflux, esophageal cancer, gastric ulcer, duodenal ulcer, acute gastritis, chronic gastritis, and gastric cancer), 4 lower gastrointestinal diseases (irritable bowel syndrome, diverticular disease, Crohn’s disease, and ulcerative colitis), 8 hepatobiliary and pancreatic diseases (non-alcoholic fatty liver disease, alcoholic liver disease, cirrhosis, liver cancer, cholecystitis, cholelithiasis, and acute and chronic pancreatitis), and acute appendicitis. Fifteen out of 20 associations persisted after adjusting for genetically predicted alcohol consumption. Genetically predicted higher alcohol consumption was associated with increased risk of duodenal ulcer, alcoholic liver disease, cirrhosis, and chronic pancreatitis; however, the association for duodenal ulcer did not remain statistically significant after adjustment for genetic predisposition to smoking initiation. CONCLUSIONS: This study provides MR evidence supporting causal associations of smoking with a broad range of gastrointestinal diseases, whereas alcohol consumption was associated with only a few gastrointestinal diseases. FUNDING: The Natural Science Fund for Distinguished Young Scholars of Zhejiang Province; National Natural Science Foundation of China; Key Project of Research and Development Plan of Hunan Province; the Swedish Heart Lung Foundation; the Swedish Research Council; the Swedish Cancer Society. eLife Sciences Publications, Ltd 2023-02-02 /pmc/articles/PMC10017103/ /pubmed/36727839 http://dx.doi.org/10.7554/eLife.84051 Text en © 2023, Yuan, Chen, Ruan et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Epidemiology and Global Health
Yuan, Shuai
Chen, Jie
Ruan, Xixian
Sun, Yuhao
Zhang, Ke
Wang, Xiaoyan
Li, Xue
Gill, Dipender
Burgess, Stephen
Giovannucci, Edward
Larsson, Susanna C
Smoking, alcohol consumption, and 24 gastrointestinal diseases: Mendelian randomization analysis
title Smoking, alcohol consumption, and 24 gastrointestinal diseases: Mendelian randomization analysis
title_full Smoking, alcohol consumption, and 24 gastrointestinal diseases: Mendelian randomization analysis
title_fullStr Smoking, alcohol consumption, and 24 gastrointestinal diseases: Mendelian randomization analysis
title_full_unstemmed Smoking, alcohol consumption, and 24 gastrointestinal diseases: Mendelian randomization analysis
title_short Smoking, alcohol consumption, and 24 gastrointestinal diseases: Mendelian randomization analysis
title_sort smoking, alcohol consumption, and 24 gastrointestinal diseases: mendelian randomization analysis
topic Epidemiology and Global Health
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10017103/
https://www.ncbi.nlm.nih.gov/pubmed/36727839
http://dx.doi.org/10.7554/eLife.84051
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