Cargando…
Evaluating the Causal Association between Inflammatory Bowel Disease and Risk of Atherosclerotic Cardiovascular Disease: Univariable and Multivariable Mendelian Randomization Study
Background: Observational studies suggested that inflammatory bowel disease (IBD) (i.e., Crohn’s disease [CD] and ulcerative colitis [UC]) is associated with an increased risk of atherosclerotic cardiovascular disease (ASCVD), including coronary artery disease (CAD) and ischemic stroke. However, it...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10526051/ https://www.ncbi.nlm.nih.gov/pubmed/37760983 http://dx.doi.org/10.3390/biomedicines11092543 |
_version_ | 1785110930354339840 |
---|---|
author | Liu, Baike Qin, Zijian Cai, Zhaolun Liu, Zheran Chen, Yun-Lin Yin, Xiaonan Yin, Yuan Peng, Xingchen Zhang, Bo |
author_facet | Liu, Baike Qin, Zijian Cai, Zhaolun Liu, Zheran Chen, Yun-Lin Yin, Xiaonan Yin, Yuan Peng, Xingchen Zhang, Bo |
author_sort | Liu, Baike |
collection | PubMed |
description | Background: Observational studies suggested that inflammatory bowel disease (IBD) (i.e., Crohn’s disease [CD] and ulcerative colitis [UC]) is associated with an increased risk of atherosclerotic cardiovascular disease (ASCVD), including coronary artery disease (CAD) and ischemic stroke. However, it is still unclear whether the observed associations causally exist. Thus, we aim to examine the potential effect of IBD, CD, and UC on the risk of CAD and ischemic stroke, using a two-sample Mendelian randomization (MR) study. Methods: Genetic instruments for IBD, CD, and UC were retrieved from the latest published genome-wide association studies (GWASs) of European ancestry. GWAS summary data for instrument–outcome associations were gathered from four independent resources: CARDIoGRAMplusC4D Consortium, MEGASTROKE consortium, FinnGen, and UK Biobank. The inverse variance weighted (IVW) method and multiple pleiotropy-robust approaches were conducted and, subsequently, combined in a fixed-effect meta-analysis. Moreover, multivariable MR (MVMR) analysis was conducted to adjust for potential influencing instrumental variables. Results: The IVW method revealed no causal effect of IBD on the risk of CAD (overall IBD on CAD: OR 1.003, 95%CI 0.982 to 1.025; CD on CAD: OR 0.997, 95%CI 0.978 to 1.016; UC on CAD: OR 0.986, 95%CI 0.963 to 1.010) or the risk of ischemic stroke (overall IBD on ischemic stroke: OR 0.994, 95%CI 0.970 to 1.018; CD on ischemic stroke: OR 0.996, 95%CI 0.979 to 1.014; UC on ischemic stroke: OR 0.999, 95%CI 0.978 to 1.020). The results of the meta-analysis and MVMR remained consistent. Conclusion: Our MR analysis does not support a causal effect of IBD on CAD and ischemic stroke, and previous results from observational studies might be biased through uncontrolled confoundings (such as IBD-specific medications and detection bias, etc.) that warrant further research. |
format | Online Article Text |
id | pubmed-10526051 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-105260512023-09-28 Evaluating the Causal Association between Inflammatory Bowel Disease and Risk of Atherosclerotic Cardiovascular Disease: Univariable and Multivariable Mendelian Randomization Study Liu, Baike Qin, Zijian Cai, Zhaolun Liu, Zheran Chen, Yun-Lin Yin, Xiaonan Yin, Yuan Peng, Xingchen Zhang, Bo Biomedicines Article Background: Observational studies suggested that inflammatory bowel disease (IBD) (i.e., Crohn’s disease [CD] and ulcerative colitis [UC]) is associated with an increased risk of atherosclerotic cardiovascular disease (ASCVD), including coronary artery disease (CAD) and ischemic stroke. However, it is still unclear whether the observed associations causally exist. Thus, we aim to examine the potential effect of IBD, CD, and UC on the risk of CAD and ischemic stroke, using a two-sample Mendelian randomization (MR) study. Methods: Genetic instruments for IBD, CD, and UC were retrieved from the latest published genome-wide association studies (GWASs) of European ancestry. GWAS summary data for instrument–outcome associations were gathered from four independent resources: CARDIoGRAMplusC4D Consortium, MEGASTROKE consortium, FinnGen, and UK Biobank. The inverse variance weighted (IVW) method and multiple pleiotropy-robust approaches were conducted and, subsequently, combined in a fixed-effect meta-analysis. Moreover, multivariable MR (MVMR) analysis was conducted to adjust for potential influencing instrumental variables. Results: The IVW method revealed no causal effect of IBD on the risk of CAD (overall IBD on CAD: OR 1.003, 95%CI 0.982 to 1.025; CD on CAD: OR 0.997, 95%CI 0.978 to 1.016; UC on CAD: OR 0.986, 95%CI 0.963 to 1.010) or the risk of ischemic stroke (overall IBD on ischemic stroke: OR 0.994, 95%CI 0.970 to 1.018; CD on ischemic stroke: OR 0.996, 95%CI 0.979 to 1.014; UC on ischemic stroke: OR 0.999, 95%CI 0.978 to 1.020). The results of the meta-analysis and MVMR remained consistent. Conclusion: Our MR analysis does not support a causal effect of IBD on CAD and ischemic stroke, and previous results from observational studies might be biased through uncontrolled confoundings (such as IBD-specific medications and detection bias, etc.) that warrant further research. MDPI 2023-09-15 /pmc/articles/PMC10526051/ /pubmed/37760983 http://dx.doi.org/10.3390/biomedicines11092543 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Liu, Baike Qin, Zijian Cai, Zhaolun Liu, Zheran Chen, Yun-Lin Yin, Xiaonan Yin, Yuan Peng, Xingchen Zhang, Bo Evaluating the Causal Association between Inflammatory Bowel Disease and Risk of Atherosclerotic Cardiovascular Disease: Univariable and Multivariable Mendelian Randomization Study |
title | Evaluating the Causal Association between Inflammatory Bowel Disease and Risk of Atherosclerotic Cardiovascular Disease: Univariable and Multivariable Mendelian Randomization Study |
title_full | Evaluating the Causal Association between Inflammatory Bowel Disease and Risk of Atherosclerotic Cardiovascular Disease: Univariable and Multivariable Mendelian Randomization Study |
title_fullStr | Evaluating the Causal Association between Inflammatory Bowel Disease and Risk of Atherosclerotic Cardiovascular Disease: Univariable and Multivariable Mendelian Randomization Study |
title_full_unstemmed | Evaluating the Causal Association between Inflammatory Bowel Disease and Risk of Atherosclerotic Cardiovascular Disease: Univariable and Multivariable Mendelian Randomization Study |
title_short | Evaluating the Causal Association between Inflammatory Bowel Disease and Risk of Atherosclerotic Cardiovascular Disease: Univariable and Multivariable Mendelian Randomization Study |
title_sort | evaluating the causal association between inflammatory bowel disease and risk of atherosclerotic cardiovascular disease: univariable and multivariable mendelian randomization study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10526051/ https://www.ncbi.nlm.nih.gov/pubmed/37760983 http://dx.doi.org/10.3390/biomedicines11092543 |
work_keys_str_mv | AT liubaike evaluatingthecausalassociationbetweeninflammatoryboweldiseaseandriskofatheroscleroticcardiovasculardiseaseunivariableandmultivariablemendelianrandomizationstudy AT qinzijian evaluatingthecausalassociationbetweeninflammatoryboweldiseaseandriskofatheroscleroticcardiovasculardiseaseunivariableandmultivariablemendelianrandomizationstudy AT caizhaolun evaluatingthecausalassociationbetweeninflammatoryboweldiseaseandriskofatheroscleroticcardiovasculardiseaseunivariableandmultivariablemendelianrandomizationstudy AT liuzheran evaluatingthecausalassociationbetweeninflammatoryboweldiseaseandriskofatheroscleroticcardiovasculardiseaseunivariableandmultivariablemendelianrandomizationstudy AT chenyunlin evaluatingthecausalassociationbetweeninflammatoryboweldiseaseandriskofatheroscleroticcardiovasculardiseaseunivariableandmultivariablemendelianrandomizationstudy AT yinxiaonan evaluatingthecausalassociationbetweeninflammatoryboweldiseaseandriskofatheroscleroticcardiovasculardiseaseunivariableandmultivariablemendelianrandomizationstudy AT yinyuan evaluatingthecausalassociationbetweeninflammatoryboweldiseaseandriskofatheroscleroticcardiovasculardiseaseunivariableandmultivariablemendelianrandomizationstudy AT pengxingchen evaluatingthecausalassociationbetweeninflammatoryboweldiseaseandriskofatheroscleroticcardiovasculardiseaseunivariableandmultivariablemendelianrandomizationstudy AT zhangbo evaluatingthecausalassociationbetweeninflammatoryboweldiseaseandriskofatheroscleroticcardiovasculardiseaseunivariableandmultivariablemendelianrandomizationstudy |