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Re-defining iron deficiency in patients with heart failure
J J Cuthbert1,2, N Ransome3, A L Clark2
1Department of Cardiorespiratory Medicine, Centre for Clinical Sciences, Hull York Medical School, University of Hull, Kingston-Upon-Hull, UK.
Insights
Iron deficiency in chronic heart failure (CHF) is common and impacts prognosis. Current diagnostic methods may be flawed, suggesting a need for better indicators to guide intravenous iron therapy in CHF patients.
Area of Science:
- Cardiology
- Hematology
- Internal Medicine
Background:
- Iron deficiency (ID) is prevalent in patients with chronic heart failure (CHF), negatively affecting symptoms and outcomes, irrespective of anemia.
- Randomized controlled trials (RCTs) investigating intravenous (IV) iron for ID in CHF have yielded conflicting results.
- This review examines the current understanding and future directions for diagnosing and managing ID in CHF.
Purpose of the Study:
- To review the definition and treatment of iron deficiency in chronic heart failure.
- To evaluate the limitations of current diagnostic criteria for iron deficiency in CHF.
- To explore alternative biomarkers for identifying high-risk patients who may benefit from IV iron.
Main Methods:
- Literature review of existing studies on iron deficiency in chronic heart failure.
- Analysis of current guideline definitions for iron deficiency.
- Evaluation of observational data and alternative diagnostic markers.
Main Results:
- The current definition of ID (serum ferritin <100 µg/L or ferritin 100-299 µg/L and TSAT <20%) is derived from studies in end-stage renal failure and may be inadequate for CHF.
- Inflammatory cytokines in CHF can affect ferritin levels, potentially masking true iron deficiency.
- Observational data suggest the current definition fails to identify a high-risk population in CHF.
Conclusions:
- The existing definition of iron deficiency in CHF may not accurately identify patients who would benefit from IV iron therapy.
- Alternative markers like low serum iron or transferrin saturation (TSAT) may be more effective in identifying at-risk CHF patients.
- Further research is needed to refine diagnostic criteria and optimize IV iron treatment strategies for ID in CHF.
Introduction:
Iron deficiency (ID) is common in patients with chronic heart failure (CHF) and is associated with worse symptoms and prognosis regardless of whether anemia is also present. However, randomized controlled trials (RCT) of intravenous (IV) iron in patients with CHF have produced inconsistent results. This review considers the past, present, and future of defining and treating ID in patients with CHF.
Areas Covered:
The current guideline definition of ID is a serum ferritin <100 µg/L or serum ferritin 100-299 µg/L and transferrin saturation (TSAT) <20% derived from trials of IV iron in patients with end-stage renal failure. Ferritin synthesis and secretion is promoted by inflammatory cytokines which are raised in patients with CHF; thus, using ferritin to define iron deficiency in patients with CHF may be flawed. Observational data suggest that the current definition of iron deficiency in CHF does not identify a high-risk population.
Expert Opinion:
Alternative indicators of ID such as low serum iron concentrations or TSAT may better identify patients with ID who are at greater risk of adverse outcome and thus, possibly, more likely to benefit from IV iron.
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