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Iron deficiency and cardiovascular disease
Iron deficiency (ID) is common in patients with cardiovascular disease. Up to 60% of patients with coronary artery disease, and an even higher proportion of those with heart failure (HF) or pulmonary hypertension have ID; the evidence for cerebrovascular disease, aortic stenosis and atrial fibrillat...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9805408/ https://www.ncbi.nlm.nih.gov/pubmed/36282723 http://dx.doi.org/10.1093/eurheartj/ehac569 |
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author | Savarese, Gianluigi von Haehling, Stephan Butler, Javed Cleland, John G F Ponikowski, Piotr Anker, Stefan D |
author_facet | Savarese, Gianluigi von Haehling, Stephan Butler, Javed Cleland, John G F Ponikowski, Piotr Anker, Stefan D |
author_sort | Savarese, Gianluigi |
collection | PubMed |
description | Iron deficiency (ID) is common in patients with cardiovascular disease. Up to 60% of patients with coronary artery disease, and an even higher proportion of those with heart failure (HF) or pulmonary hypertension have ID; the evidence for cerebrovascular disease, aortic stenosis and atrial fibrillation is less robust. The prevalence of ID increases with the severity of cardiac and renal dysfunction and is probably more common amongst women. Insufficient dietary iron, reduced iron absorption due to increases in hepcidin secondary to the low-grade inflammation associated with atherosclerosis and congestion or reduced gastric acidity, and increased blood loss due to anti-thrombotic therapy or gastro-intestinal or renal disease may all cause ID. For older people in the general population and patients with HF with reduced ejection fraction (HFrEF), both anaemia and ID are associated with a poor prognosis; each may confer independent risk. There is growing evidence that ID is an important therapeutic target for patients with HFrEF, even if they do not have anaemia. Whether this is also true for other HF phenotypes or patients with cardiovascular disease in general is currently unknown. Randomized trials showed that intravenous ferric carboxymaltose improved symptoms, health-related quality of life and exercise capacity and reduced hospitalizations for worsening HF in patients with HFrEF and mildly reduced ejection fraction (<50%). Since ID is easy to treat and is effective for patients with HFrEF, such patients should be investigated for possible ID. This recommendation may extend to other populations in the light of evidence from future trials. |
format | Online Article Text |
id | pubmed-9805408 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-98054082023-01-03 Iron deficiency and cardiovascular disease Savarese, Gianluigi von Haehling, Stephan Butler, Javed Cleland, John G F Ponikowski, Piotr Anker, Stefan D Eur Heart J State of the Art Review Iron deficiency (ID) is common in patients with cardiovascular disease. Up to 60% of patients with coronary artery disease, and an even higher proportion of those with heart failure (HF) or pulmonary hypertension have ID; the evidence for cerebrovascular disease, aortic stenosis and atrial fibrillation is less robust. The prevalence of ID increases with the severity of cardiac and renal dysfunction and is probably more common amongst women. Insufficient dietary iron, reduced iron absorption due to increases in hepcidin secondary to the low-grade inflammation associated with atherosclerosis and congestion or reduced gastric acidity, and increased blood loss due to anti-thrombotic therapy or gastro-intestinal or renal disease may all cause ID. For older people in the general population and patients with HF with reduced ejection fraction (HFrEF), both anaemia and ID are associated with a poor prognosis; each may confer independent risk. There is growing evidence that ID is an important therapeutic target for patients with HFrEF, even if they do not have anaemia. Whether this is also true for other HF phenotypes or patients with cardiovascular disease in general is currently unknown. Randomized trials showed that intravenous ferric carboxymaltose improved symptoms, health-related quality of life and exercise capacity and reduced hospitalizations for worsening HF in patients with HFrEF and mildly reduced ejection fraction (<50%). Since ID is easy to treat and is effective for patients with HFrEF, such patients should be investigated for possible ID. This recommendation may extend to other populations in the light of evidence from future trials. Oxford University Press 2022-10-25 /pmc/articles/PMC9805408/ /pubmed/36282723 http://dx.doi.org/10.1093/eurheartj/ehac569 Text en © The Author(s) 2022. 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 | State of the Art Review Savarese, Gianluigi von Haehling, Stephan Butler, Javed Cleland, John G F Ponikowski, Piotr Anker, Stefan D Iron deficiency and cardiovascular disease |
title | Iron deficiency and cardiovascular disease |
title_full | Iron deficiency and cardiovascular disease |
title_fullStr | Iron deficiency and cardiovascular disease |
title_full_unstemmed | Iron deficiency and cardiovascular disease |
title_short | Iron deficiency and cardiovascular disease |
title_sort | iron deficiency and cardiovascular disease |
topic | State of the Art Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9805408/ https://www.ncbi.nlm.nih.gov/pubmed/36282723 http://dx.doi.org/10.1093/eurheartj/ehac569 |
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