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Inflammatory bowel disease and celiac disease: A bidirectional Mendelian randomization study

Objective: Although previous epidemiological studies have reported substantial links between inflammatory bowel disease (IBD), including Crohn’s disease (CD) and ulcerative colitis (UC), and celiac disease (CeD), the causal relationship between the two remains unknown. The purpose of the current stu...

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Autores principales: Shi, Yue, Feng, Sijia, Yan, Mengdie, Wei, Shuyan, Yang, Kejia, Feng, Yue
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9437575/
https://www.ncbi.nlm.nih.gov/pubmed/36061176
http://dx.doi.org/10.3389/fgene.2022.928944
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author Shi, Yue
Feng, Sijia
Yan, Mengdie
Wei, Shuyan
Yang, Kejia
Feng, Yue
author_facet Shi, Yue
Feng, Sijia
Yan, Mengdie
Wei, Shuyan
Yang, Kejia
Feng, Yue
author_sort Shi, Yue
collection PubMed
description Objective: Although previous epidemiological studies have reported substantial links between inflammatory bowel disease (IBD), including Crohn’s disease (CD) and ulcerative colitis (UC), and celiac disease (CeD), the causal relationship between the two remains unknown. The purpose of the current study was to evaluate the bidirectional causation between IBD and CeD using Mendelian randomization (MR). Method: We obtained genome-wide association study (GWAS) summary data of IBD (CD and UC) and CeD of thoroughly European ancestry from the IEU GWAS database. We screened eligible instrumental variables (IVs) according to the three assumptions of MR. MR was performed using MR-Egger, weighted median (WM), and inverse variance weighted (IVW) methods. The MR-Egger intercept and MR-PRESSO method investigated the horizontal pleiotropy effect. A leave-one-out analysis was performed to prevent bias caused by a single SNP. Results: The study assessed a bidirectional causal effect between CD and CeD; CD increased the risk of CeD (IVW odds ratio (OR) = 1.27, 95% confidence interval (CI) = 1.19–1.35, p = 3.75E-13) and vice-a-versa (IVW OR = 1.09, 95% CI = 1.05–1.13, p = 1.39E-05). Additionally, CeD was influenced by IBD (IVW OR = 1.24, 95% CI = 1.16–1.34, p = 9.42E-10) and UC (IVW OR = 0.90, 95% CI = 0.83–0.98, p = 0.017). However, we observed no evidence of a causal relationship between CeD and IBD (IVW OR = 1.00, 95% CI = 0.97–1.04, p = 0.900) or UC (IVW OR = 0.96, 95% CI = 0.92–1.02, p = 0.172). Conclusion: The present study revealed that IBD and CeD have a bidirectional causal relationship. However, it is slightly different from the results of previous observational studies, recommending that future studies focus on the mechanisms of interaction between CD and CeD.
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spelling pubmed-94375752022-09-03 Inflammatory bowel disease and celiac disease: A bidirectional Mendelian randomization study Shi, Yue Feng, Sijia Yan, Mengdie Wei, Shuyan Yang, Kejia Feng, Yue Front Genet Genetics Objective: Although previous epidemiological studies have reported substantial links between inflammatory bowel disease (IBD), including Crohn’s disease (CD) and ulcerative colitis (UC), and celiac disease (CeD), the causal relationship between the two remains unknown. The purpose of the current study was to evaluate the bidirectional causation between IBD and CeD using Mendelian randomization (MR). Method: We obtained genome-wide association study (GWAS) summary data of IBD (CD and UC) and CeD of thoroughly European ancestry from the IEU GWAS database. We screened eligible instrumental variables (IVs) according to the three assumptions of MR. MR was performed using MR-Egger, weighted median (WM), and inverse variance weighted (IVW) methods. The MR-Egger intercept and MR-PRESSO method investigated the horizontal pleiotropy effect. A leave-one-out analysis was performed to prevent bias caused by a single SNP. Results: The study assessed a bidirectional causal effect between CD and CeD; CD increased the risk of CeD (IVW odds ratio (OR) = 1.27, 95% confidence interval (CI) = 1.19–1.35, p = 3.75E-13) and vice-a-versa (IVW OR = 1.09, 95% CI = 1.05–1.13, p = 1.39E-05). Additionally, CeD was influenced by IBD (IVW OR = 1.24, 95% CI = 1.16–1.34, p = 9.42E-10) and UC (IVW OR = 0.90, 95% CI = 0.83–0.98, p = 0.017). However, we observed no evidence of a causal relationship between CeD and IBD (IVW OR = 1.00, 95% CI = 0.97–1.04, p = 0.900) or UC (IVW OR = 0.96, 95% CI = 0.92–1.02, p = 0.172). Conclusion: The present study revealed that IBD and CeD have a bidirectional causal relationship. However, it is slightly different from the results of previous observational studies, recommending that future studies focus on the mechanisms of interaction between CD and CeD. Frontiers Media S.A. 2022-08-19 /pmc/articles/PMC9437575/ /pubmed/36061176 http://dx.doi.org/10.3389/fgene.2022.928944 Text en Copyright © 2022 Shi, Feng, Yan, Wei, Yang and Feng. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Shi, Yue
Feng, Sijia
Yan, Mengdie
Wei, Shuyan
Yang, Kejia
Feng, Yue
Inflammatory bowel disease and celiac disease: A bidirectional Mendelian randomization study
title Inflammatory bowel disease and celiac disease: A bidirectional Mendelian randomization study
title_full Inflammatory bowel disease and celiac disease: A bidirectional Mendelian randomization study
title_fullStr Inflammatory bowel disease and celiac disease: A bidirectional Mendelian randomization study
title_full_unstemmed Inflammatory bowel disease and celiac disease: A bidirectional Mendelian randomization study
title_short Inflammatory bowel disease and celiac disease: A bidirectional Mendelian randomization study
title_sort inflammatory bowel disease and celiac disease: a bidirectional mendelian randomization study
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9437575/
https://www.ncbi.nlm.nih.gov/pubmed/36061176
http://dx.doi.org/10.3389/fgene.2022.928944
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