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Bidirectional causal link between inflammatory bowel disease and celiac disease: A two-sample mendelian randomization analysis

Background: Observational research has shown a correlation between inflammatory bowel disease (IBD) [comprising ulcerative colitis (UC) and Crohn’s disease (CD)] and celiac disease. However, the relationship between these two diseases remains uncertain. Methods: We utilized two-sample Mendelian rand...

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Autores principales: A, Gu, Sun, Caixia, Shan, Yuezhan, Husile, Husile, Bai, Haihua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9530974/
https://www.ncbi.nlm.nih.gov/pubmed/36204317
http://dx.doi.org/10.3389/fgene.2022.993492
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author A, Gu
Sun, Caixia
Shan, Yuezhan
Husile, Husile
Bai, Haihua
author_facet A, Gu
Sun, Caixia
Shan, Yuezhan
Husile, Husile
Bai, Haihua
author_sort A, Gu
collection PubMed
description Background: Observational research has shown a correlation between inflammatory bowel disease (IBD) [comprising ulcerative colitis (UC) and Crohn’s disease (CD)] and celiac disease. However, the relationship between these two diseases remains uncertain. Methods: We utilized two-sample Mendelian randomization (MR) to estimate the bidirectional causal relationships between IBD and celiac disease. This study utilized data on single nucleotide polymorphisms (SNPs) from genome-wide association studies (GWASs). Heterogeneity, pleiotropy, and sensitivity analyses were also performed to evaluate the MR results. Results: There was a significant causal relationship between IBD and CD and celiac disease (e.g., IBD and celiac disease, inverse variance weighting (IVW) odds ratio (OR) = 1.0828, 95% CI = 1.0258–1.1428, p = 0.0039; CD and celiac disease, IVW OR = 1.0807, 95% CI = 1.0227–1.1420, p = 0.0058). However, in the reverse direction, we found only suggestive positive causality between celiac disease and CD (e.g., IVW OR = 1.0366, 95% CI = 1.0031–1.0711, p = 0.0319). No evidence of heterogeneity between genetic variants was found (e.g., IBD vs. celiac disease, MR-Egger Q = 47.4391, p = 0.6159). Horizontal pleiotropy hardly influenced causality (e.g., IBD vs. celiac disease, MR-Egger test: p = 0.4340). Leave-one-out analysis showed that individual SNPs did not influence the general results. Conclusion: Our MR analysis revealed a positive causal link between IBD and celiac disease in the European population. In addition, several recommendations for disease prevention and clinical management have been discussed.
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spelling pubmed-95309742022-10-05 Bidirectional causal link between inflammatory bowel disease and celiac disease: A two-sample mendelian randomization analysis A, Gu Sun, Caixia Shan, Yuezhan Husile, Husile Bai, Haihua Front Genet Genetics Background: Observational research has shown a correlation between inflammatory bowel disease (IBD) [comprising ulcerative colitis (UC) and Crohn’s disease (CD)] and celiac disease. However, the relationship between these two diseases remains uncertain. Methods: We utilized two-sample Mendelian randomization (MR) to estimate the bidirectional causal relationships between IBD and celiac disease. This study utilized data on single nucleotide polymorphisms (SNPs) from genome-wide association studies (GWASs). Heterogeneity, pleiotropy, and sensitivity analyses were also performed to evaluate the MR results. Results: There was a significant causal relationship between IBD and CD and celiac disease (e.g., IBD and celiac disease, inverse variance weighting (IVW) odds ratio (OR) = 1.0828, 95% CI = 1.0258–1.1428, p = 0.0039; CD and celiac disease, IVW OR = 1.0807, 95% CI = 1.0227–1.1420, p = 0.0058). However, in the reverse direction, we found only suggestive positive causality between celiac disease and CD (e.g., IVW OR = 1.0366, 95% CI = 1.0031–1.0711, p = 0.0319). No evidence of heterogeneity between genetic variants was found (e.g., IBD vs. celiac disease, MR-Egger Q = 47.4391, p = 0.6159). Horizontal pleiotropy hardly influenced causality (e.g., IBD vs. celiac disease, MR-Egger test: p = 0.4340). Leave-one-out analysis showed that individual SNPs did not influence the general results. Conclusion: Our MR analysis revealed a positive causal link between IBD and celiac disease in the European population. In addition, several recommendations for disease prevention and clinical management have been discussed. Frontiers Media S.A. 2022-09-20 /pmc/articles/PMC9530974/ /pubmed/36204317 http://dx.doi.org/10.3389/fgene.2022.993492 Text en Copyright © 2022 A, Sun, Shan, Husile and Bai. 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
A, Gu
Sun, Caixia
Shan, Yuezhan
Husile, Husile
Bai, Haihua
Bidirectional causal link between inflammatory bowel disease and celiac disease: A two-sample mendelian randomization analysis
title Bidirectional causal link between inflammatory bowel disease and celiac disease: A two-sample mendelian randomization analysis
title_full Bidirectional causal link between inflammatory bowel disease and celiac disease: A two-sample mendelian randomization analysis
title_fullStr Bidirectional causal link between inflammatory bowel disease and celiac disease: A two-sample mendelian randomization analysis
title_full_unstemmed Bidirectional causal link between inflammatory bowel disease and celiac disease: A two-sample mendelian randomization analysis
title_short Bidirectional causal link between inflammatory bowel disease and celiac disease: A two-sample mendelian randomization analysis
title_sort bidirectional causal link between inflammatory bowel disease and celiac disease: a two-sample mendelian randomization analysis
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9530974/
https://www.ncbi.nlm.nih.gov/pubmed/36204317
http://dx.doi.org/10.3389/fgene.2022.993492
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