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Published on: May 10, 2022
Iron deficiency and cardiovascular disease
Gianluigi Savarese1,2, Stephan von Haehling3,4, Javed Butler5,6
1Division of Cardiology, Department of Medicine, Karolinska Institutet, Stockholm, Sweden.
Insights
Iron deficiency (ID) is a common issue in cardiovascular disease patients. Treating ID with intravenous iron in heart failure patients with reduced ejection fraction improves outcomes and quality of life.
Area of Science:
- Cardiology
- Hematology
- Internal Medicine
Background:
- Iron deficiency (ID) is highly prevalent in cardiovascular disease (CVD), affecting up to 60% of coronary artery disease patients and a higher proportion of heart failure (HF) patients.
- ID prevalence escalates with cardiac and renal dysfunction severity and is more common in women.
- Causes of ID include inadequate intake, reduced absorption (hepcidin increase), and blood loss (e.g., from anti-thrombotic therapy).
Purpose of the Study:
- To investigate the role and therapeutic implications of iron deficiency in cardiovascular disease.
- To evaluate the efficacy of iron supplementation in heart failure with reduced ejection fraction (HFrEF).
Main Methods:
- Review of existing literature and evidence regarding iron deficiency in various cardiovascular conditions.
- Analysis of randomized trials investigating intravenous iron therapy in HFrEF patients.
Main Results:
- Iron deficiency is linked to poor prognosis in older adults and HFrEF patients, potentially conferring independent risk.
- Intravenous ferric carboxymaltose improved symptoms, quality of life, exercise capacity, and reduced HF hospitalizations in HFrEF patients (<50% ejection fraction).
Conclusions:
- Iron deficiency is a significant and treatable factor in HFrEF, warranting investigation even in non-anemic patients.
- Intravenous iron therapy is effective for HFrEF patients, suggesting broader applicability in CVD populations pending further research.
Abstract:
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.
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