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Inflammatory bowel disease and cardiovascular disease: A two-sample Mendelian randomization analysis
BACKGROUND: Although epidemiological studies have shown a positive relationship between inflammatory bowel disease (IBD) and risk of cardiovascular disease (CVD) outcomes, a solid causal relationship has not been established. Thus, a two-sample Mendelian randomization (MR) study was conducted to exp...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9478388/ https://www.ncbi.nlm.nih.gov/pubmed/36119744 http://dx.doi.org/10.3389/fcvm.2022.927120 |
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author | Wu, Kaiwen Li, Aoshuang Liu, Lei Shu, Tao Xia, Demeng Sun, Xiaobin |
author_facet | Wu, Kaiwen Li, Aoshuang Liu, Lei Shu, Tao Xia, Demeng Sun, Xiaobin |
author_sort | Wu, Kaiwen |
collection | PubMed |
description | BACKGROUND: Although epidemiological studies have shown a positive relationship between inflammatory bowel disease (IBD) and risk of cardiovascular disease (CVD) outcomes, a solid causal relationship has not been established. Thus, a two-sample Mendelian randomization (MR) study was conducted to explore the potential causal effect between IBD and CVD outcomes. METHODS: We performed a two-sample MR analysis to analyze the causal effect of the IBD on CVD outcome by using summary-level genome-wide association studies of European descent. The inverse-variance weighted (IVW) method was used as the main MR analysis, with complementary analyses of MR Egger, maximum likelihood, weighted median, penalized weighted media, simple mode, weighted mode, and MR-PRESSO methods. Multiple sensitivity analyses were used to evaluate the robustness of our results. RESULTS: All P-values were greater than 0.05 in the IVW method, showing no evidence of a causal association between circulating IBD and CVD. Similar results were observed by using other MR methods. No evidence of heterogeneity, pleiotropy, or outlier single-nucleotide polymorphisms was detected. Sensitivity analyses demonstrated the robustness of the results. CONCLUSION: The findings of this study provided no evidence to support that IBD has a large effect on risk of CVD outcomes, which is in contrast to many previous observational reports. Further studies are needed to determine the potential mechanism of association identified in observational studies. |
format | Online Article Text |
id | pubmed-9478388 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-94783882022-09-17 Inflammatory bowel disease and cardiovascular disease: A two-sample Mendelian randomization analysis Wu, Kaiwen Li, Aoshuang Liu, Lei Shu, Tao Xia, Demeng Sun, Xiaobin Front Cardiovasc Med Cardiovascular Medicine BACKGROUND: Although epidemiological studies have shown a positive relationship between inflammatory bowel disease (IBD) and risk of cardiovascular disease (CVD) outcomes, a solid causal relationship has not been established. Thus, a two-sample Mendelian randomization (MR) study was conducted to explore the potential causal effect between IBD and CVD outcomes. METHODS: We performed a two-sample MR analysis to analyze the causal effect of the IBD on CVD outcome by using summary-level genome-wide association studies of European descent. The inverse-variance weighted (IVW) method was used as the main MR analysis, with complementary analyses of MR Egger, maximum likelihood, weighted median, penalized weighted media, simple mode, weighted mode, and MR-PRESSO methods. Multiple sensitivity analyses were used to evaluate the robustness of our results. RESULTS: All P-values were greater than 0.05 in the IVW method, showing no evidence of a causal association between circulating IBD and CVD. Similar results were observed by using other MR methods. No evidence of heterogeneity, pleiotropy, or outlier single-nucleotide polymorphisms was detected. Sensitivity analyses demonstrated the robustness of the results. CONCLUSION: The findings of this study provided no evidence to support that IBD has a large effect on risk of CVD outcomes, which is in contrast to many previous observational reports. Further studies are needed to determine the potential mechanism of association identified in observational studies. Frontiers Media S.A. 2022-09-02 /pmc/articles/PMC9478388/ /pubmed/36119744 http://dx.doi.org/10.3389/fcvm.2022.927120 Text en Copyright © 2022 Wu, Li, Liu, Shu, Xia and Sun. 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 | Cardiovascular Medicine Wu, Kaiwen Li, Aoshuang Liu, Lei Shu, Tao Xia, Demeng Sun, Xiaobin Inflammatory bowel disease and cardiovascular disease: A two-sample Mendelian randomization analysis |
title | Inflammatory bowel disease and cardiovascular disease: A two-sample Mendelian randomization analysis |
title_full | Inflammatory bowel disease and cardiovascular disease: A two-sample Mendelian randomization analysis |
title_fullStr | Inflammatory bowel disease and cardiovascular disease: A two-sample Mendelian randomization analysis |
title_full_unstemmed | Inflammatory bowel disease and cardiovascular disease: A two-sample Mendelian randomization analysis |
title_short | Inflammatory bowel disease and cardiovascular disease: A two-sample Mendelian randomization analysis |
title_sort | inflammatory bowel disease and cardiovascular disease: a two-sample mendelian randomization analysis |
topic | Cardiovascular Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9478388/ https://www.ncbi.nlm.nih.gov/pubmed/36119744 http://dx.doi.org/10.3389/fcvm.2022.927120 |
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