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Imbalance of Iron Availability and Demand in Patients With Acute and Chronic Heart Failure
Lukas Lanser1, Gerhard Poelzl2, Moritz Messner2
1Department of Internal Medicine II Medical University of Innsbruck Innsbruck Austria.
Insights
Iron deficiency (ID) is common in heart failure patients. Current definitions may overestimate ID, suggesting more specific criteria are needed to identify patients who benefit from iron supplementation.
Area of Science:
- Cardiology
- Hematology
- Biochemistry
Background:
- Iron deficiency (ID) is a significant comorbidity in acute (AHF) and chronic heart failure (CHF) patients, linked to increased morbidity and mortality.
- Understanding iron homeostasis is crucial for managing heart failure patients.
Purpose of the Study:
- To characterize iron homeostasis in heart failure patients using various biomarkers.
- To evaluate the accuracy of current European Society of Cardiology/American College of Cardiology/American Heart Association (ESC/ACC/AHA) ID definitions in reflecting tissue iron status.
Main Methods:
- Retrospective cohort study of 277 AHF and 476 CHF patients.
- Analysis of biomarkers including ferritin, transferrin saturation, soluble transferrin receptor, hepcidin, and reticulocyte hemoglobin.
- Evaluation of current ESC/ACC/AHA ID definition accuracy.
Main Results:
- AHF patients exhibited more advanced ID than CHF patients.
- Current ID definitions identified ID in a significant proportion of patients, but biomarker analysis suggested overestimation, particularly in CHF.
- More specific ID criteria could reduce unnecessary iron supplementation by up to 65.6% in CHF patients.
Conclusions:
- The current ESC/ACC/AHA-based ID definition may overestimate true ID in heart failure, especially in CHF.
- Stricter ID thresholds could better identify heart failure patients with reduced tissue iron availability who would benefit from intravenous iron therapy.
Background:
Iron deficiency (ID) is a frequent comorbidity in patients with acute (AHF) and chronic heart failure (CHF) associated with morbidity and death. We aimed to better characterize iron homeostasis in patients with heart failure applying different biomarkers and to evaluate the accuracy of current ID definition by the European Society of Cardiology/American College of Cardiology/American Heart Association to indicate tissue iron availability and demand.
Methods And Results:
We performed a retrospective cohort study investigating 277 patients with AHF and 476 patients with CHF between February 2021 and May 2022. Patients with AHF had more advanced ID than patients with CHF, reflected by increased soluble transferrin receptor and soluble transferrin receptor-ferritin index, and lower ferritin, serum iron, transferrin saturation, hepcidin, and reticulocyte hemoglobin. Decreased iron availability or increased tissue iron demand, reflected by increased soluble transferrin receptor-ferritin index and decreased reticulocyte hemoglobin, was found in 84.1% (AHF) and 28.0% (CHF) with absolute ID and in 50.0% (AHF) and 10.5% (CHF) with combined ID according to the current European Society of Cardiology/American College of Cardiology/American Heart Association-based ID definition. Low hepcidin expression as an indicator of systemic ID was found in 91.1% (AHF) and 80.4% (CHF) of patients with absolute ID and in 32.3% (AHF) and 18.8% (CHF) of patients with combined ID. ID definitions with higher specificity reduce the need for iron supplementation by 25.5% in patients with AHF and by 65.6% in patients with CHF.
Conclusions:
Our results suggest that the current European Society of Cardiology/American College of Cardiology/American Heart Association-based ID definition might overestimate true ID, particularly in CHF. More stringent thresholds for ID could more accurately identify patients with heart failure with reduced tissue iron availability who benefit from intravenous iron supplementation.
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