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Inflammatory bowel disease and cardiovascular diseases: a concise review
Cardiovascular diseases (CVDs) remain the leading cause of morbidity and mortality despite aggressive treatment of traditional risk factors. Chronic inflammation plays an important role in the initiation and progression of CVDs. Inflammatory bowel disease (IBD) is a systemic state of inflammation ex...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9242064/ https://www.ncbi.nlm.nih.gov/pubmed/35919661 http://dx.doi.org/10.1093/ehjopen/oeab029 |
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author | Wu, Hao Hu, Tingzi Hao, Hong Hill, Michael A Xu, Canxia Liu, Zhenguo |
author_facet | Wu, Hao Hu, Tingzi Hao, Hong Hill, Michael A Xu, Canxia Liu, Zhenguo |
author_sort | Wu, Hao |
collection | PubMed |
description | Cardiovascular diseases (CVDs) remain the leading cause of morbidity and mortality despite aggressive treatment of traditional risk factors. Chronic inflammation plays an important role in the initiation and progression of CVDs. Inflammatory bowel disease (IBD) is a systemic state of inflammation exhibiting increased levels of pro-inflammatory cytokines including tumour necrosis factor-α (TNF-α), interleukin (IL)-1β, and IL-6. Importantly, IBD is associated with increased risk for CVDs especially in women and young adults, including coronary artery disease, stroke, thromboembolic diseases, and arrhythmias. Potential mechanisms underlying the increased risk for CVDs in IBD patients include increased levels of inflammatory cytokines and oxidative stress, altered platelet function, hypercoagulability, decreased numbers of circulating endothelial progenitor cells, endothelial dysfunction, and possible interruption of gut microbiota. Although IBD does not appear to exacerbate the traditional risk factors for CVDs, including hypertension, hyperlipidaemia, diabetes mellitus, and obesity, aggressive risk stratifications are important for primary and secondary prevention of CVDs for IBD patients. Compared to 5-aminosalicylates and corticosteroids, anti-TNF-α therapy in IBD patients was consistently associated with decreasing cardiovascular events. In the absence of contraindications, low-dose aspirin and statins appear to be beneficial for IBD patients. Low-molecular-weight heparin is also recommended for patients who are hospitalized with acute IBD flares without major bleeding risk. A multidisciplinary team approach should be considered for the management of IBD patients. |
format | Online Article Text |
id | pubmed-9242064 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-92420642022-08-01 Inflammatory bowel disease and cardiovascular diseases: a concise review Wu, Hao Hu, Tingzi Hao, Hong Hill, Michael A Xu, Canxia Liu, Zhenguo Eur Heart J Open Review Cardiovascular diseases (CVDs) remain the leading cause of morbidity and mortality despite aggressive treatment of traditional risk factors. Chronic inflammation plays an important role in the initiation and progression of CVDs. Inflammatory bowel disease (IBD) is a systemic state of inflammation exhibiting increased levels of pro-inflammatory cytokines including tumour necrosis factor-α (TNF-α), interleukin (IL)-1β, and IL-6. Importantly, IBD is associated with increased risk for CVDs especially in women and young adults, including coronary artery disease, stroke, thromboembolic diseases, and arrhythmias. Potential mechanisms underlying the increased risk for CVDs in IBD patients include increased levels of inflammatory cytokines and oxidative stress, altered platelet function, hypercoagulability, decreased numbers of circulating endothelial progenitor cells, endothelial dysfunction, and possible interruption of gut microbiota. Although IBD does not appear to exacerbate the traditional risk factors for CVDs, including hypertension, hyperlipidaemia, diabetes mellitus, and obesity, aggressive risk stratifications are important for primary and secondary prevention of CVDs for IBD patients. Compared to 5-aminosalicylates and corticosteroids, anti-TNF-α therapy in IBD patients was consistently associated with decreasing cardiovascular events. In the absence of contraindications, low-dose aspirin and statins appear to be beneficial for IBD patients. Low-molecular-weight heparin is also recommended for patients who are hospitalized with acute IBD flares without major bleeding risk. A multidisciplinary team approach should be considered for the management of IBD patients. Oxford University Press 2021-10-14 /pmc/articles/PMC9242064/ /pubmed/35919661 http://dx.doi.org/10.1093/ehjopen/oeab029 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the European Society of Cardiology. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Review Wu, Hao Hu, Tingzi Hao, Hong Hill, Michael A Xu, Canxia Liu, Zhenguo Inflammatory bowel disease and cardiovascular diseases: a concise review |
title | Inflammatory bowel disease and cardiovascular diseases: a concise review |
title_full | Inflammatory bowel disease and cardiovascular diseases: a concise review |
title_fullStr | Inflammatory bowel disease and cardiovascular diseases: a concise review |
title_full_unstemmed | Inflammatory bowel disease and cardiovascular diseases: a concise review |
title_short | Inflammatory bowel disease and cardiovascular diseases: a concise review |
title_sort | inflammatory bowel disease and cardiovascular diseases: a concise review |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9242064/ https://www.ncbi.nlm.nih.gov/pubmed/35919661 http://dx.doi.org/10.1093/ehjopen/oeab029 |
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