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Multiple Sclerosis and the Risk of Cardiovascular Diseases: A Mendelian Randomization Study
BACKGROUND: Observational studies suggested that multiple sclerosis (MS) is associated with cardiovascular diseases (CVDs). However, the causal association has not been fully elucidated. Thus, we aim to assess the causality of the associations of MS with risk of CVDs. METHODS: A two-sample Mendelian...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8964627/ https://www.ncbi.nlm.nih.gov/pubmed/35371017 http://dx.doi.org/10.3389/fimmu.2022.861885 |
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author | Yang, Fangkun Hu, Teng He, Kewan Ying, Jiajun Cui, Hanbin |
author_facet | Yang, Fangkun Hu, Teng He, Kewan Ying, Jiajun Cui, Hanbin |
author_sort | Yang, Fangkun |
collection | PubMed |
description | BACKGROUND: Observational studies suggested that multiple sclerosis (MS) is associated with cardiovascular diseases (CVDs). However, the causal association has not been fully elucidated. Thus, we aim to assess the causality of the associations of MS with risk of CVDs. METHODS: A two-sample Mendelian randomization (MR) study was performed to explore the causality. Genetic instruments were identified for MS from a genome-wide association study (GWAS) involving 115,803 individuals. Summary-level data for CVDs were obtained from different GWAS meta-analysis studies. MR analysis was conducted mainly using the inverse-variance weighted (IVW) method. Sensitivity analyses were further performed to ensure the robustness of the results. RESULTS: This MR study found suggestive evidence that genetic liability to MS was associated with an increased risk of coronary artery disease (CAD) [odds ratio (OR), 1.02; 95% confidence interval (CI), 1.00–1.04; p = 0.03], myocardial infarction (MI) (OR, 1.03; 95% CI, 1.00–1.06; p = 0.01), heart failure (HF) (OR, 1.02; 95% CI, 1.00–1.04; p = 0.02), all-cause stroke (AS) (OR, 1.02; 95% CI, 1.00–1.05; p = 0.02), and any ischemic stroke (AIS) (OR, 1.02; 95% CI, 1.00–1.05; p = 0.04). The null-association was observed between MS and the other CVDs. Further analyses found little evidence of pleiotropy. CONCLUSIONS: We provided suggestive genetic evidence for the causal associations of MS with increased risk of CAD, MI, HF, AS, and AIS, which highlighted the significance of active monitoring and prevention of cardiovascular risk to combat cardiovascular comorbidities in MS patients. |
format | Online Article Text |
id | pubmed-8964627 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-89646272022-03-31 Multiple Sclerosis and the Risk of Cardiovascular Diseases: A Mendelian Randomization Study Yang, Fangkun Hu, Teng He, Kewan Ying, Jiajun Cui, Hanbin Front Immunol Immunology BACKGROUND: Observational studies suggested that multiple sclerosis (MS) is associated with cardiovascular diseases (CVDs). However, the causal association has not been fully elucidated. Thus, we aim to assess the causality of the associations of MS with risk of CVDs. METHODS: A two-sample Mendelian randomization (MR) study was performed to explore the causality. Genetic instruments were identified for MS from a genome-wide association study (GWAS) involving 115,803 individuals. Summary-level data for CVDs were obtained from different GWAS meta-analysis studies. MR analysis was conducted mainly using the inverse-variance weighted (IVW) method. Sensitivity analyses were further performed to ensure the robustness of the results. RESULTS: This MR study found suggestive evidence that genetic liability to MS was associated with an increased risk of coronary artery disease (CAD) [odds ratio (OR), 1.02; 95% confidence interval (CI), 1.00–1.04; p = 0.03], myocardial infarction (MI) (OR, 1.03; 95% CI, 1.00–1.06; p = 0.01), heart failure (HF) (OR, 1.02; 95% CI, 1.00–1.04; p = 0.02), all-cause stroke (AS) (OR, 1.02; 95% CI, 1.00–1.05; p = 0.02), and any ischemic stroke (AIS) (OR, 1.02; 95% CI, 1.00–1.05; p = 0.04). The null-association was observed between MS and the other CVDs. Further analyses found little evidence of pleiotropy. CONCLUSIONS: We provided suggestive genetic evidence for the causal associations of MS with increased risk of CAD, MI, HF, AS, and AIS, which highlighted the significance of active monitoring and prevention of cardiovascular risk to combat cardiovascular comorbidities in MS patients. Frontiers Media S.A. 2022-03-15 /pmc/articles/PMC8964627/ /pubmed/35371017 http://dx.doi.org/10.3389/fimmu.2022.861885 Text en Copyright © 2022 Yang, Hu, He, Ying and Cui 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 | Immunology Yang, Fangkun Hu, Teng He, Kewan Ying, Jiajun Cui, Hanbin Multiple Sclerosis and the Risk of Cardiovascular Diseases: A Mendelian Randomization Study |
title | Multiple Sclerosis and the Risk of Cardiovascular Diseases: A Mendelian Randomization Study |
title_full | Multiple Sclerosis and the Risk of Cardiovascular Diseases: A Mendelian Randomization Study |
title_fullStr | Multiple Sclerosis and the Risk of Cardiovascular Diseases: A Mendelian Randomization Study |
title_full_unstemmed | Multiple Sclerosis and the Risk of Cardiovascular Diseases: A Mendelian Randomization Study |
title_short | Multiple Sclerosis and the Risk of Cardiovascular Diseases: A Mendelian Randomization Study |
title_sort | multiple sclerosis and the risk of cardiovascular diseases: a mendelian randomization study |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8964627/ https://www.ncbi.nlm.nih.gov/pubmed/35371017 http://dx.doi.org/10.3389/fimmu.2022.861885 |
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