Criteria for Iron Deficiency in Patients With Heart Failure
- PMID: 35086656
- DOI: 10.1016/j.jacc.2021.11.039
Criteria for Iron Deficiency in Patients With Heart Failure
Abstract
Background: Guidelines on heart failure (HF) define iron deficiency (ID) as a serum ferritin <100 ng/mL or, when 100-299 ng/mL, a transferrin saturation (TSAT) <20%. Inflammation (common in HF) may hinder interpretation of serum ferritin.
Objectives: This study sought to investigate how different definitions of ID affect its prevalence and relationship to prognosis in ambulatory patients with chronic HF.
Methods: Prevalence, relationship with patients' characteristics, and outcomes of various ID definitions were evaluated among patients with HF referred to a regional clinic (Hull LifeLab) from 2001 to 2019.
Results: Of 4,422 patients with HF (median age 75 years [range: 68-82 years], 60% men, 32% with reduced left ventricular ejection fraction), 46% had TSAT <20%, 48% had serum iron ≤13 μmol/L, 57% had serum ferritin <100 ng/mL, and 68% fulfilled current guideline criteria for ID, of whom 35% had a TSAT >20%. Irrespective of definition, ID was more common in women and those with more severe symptoms, anemia, or preserved ejection fraction. TSAT <20% and serum iron ≤13 μmol/L, but not guideline criteria, were associated with higher 5-year mortality (HR: 1.27; 95% CI: 1.14-1.43; P < 0.001; and HR: 1.37; 95% CI: 1.22-1.54; P < 0.001, respectively). Serum ferritin <100 ng/mL tended to be associated with lower mortality (HR: 0.91; 95% CI: 0.81-1.01; P = 0.09).
Conclusions: Different definitions of ID provide discordant results for prevalence and prognosis. Definitions lacking specificity may attenuate the benefits of intravenous iron observed in trials while definitions lacking sensitivity may exclude patients who should receive intravenous iron. Prespecified subgroup analyses of ongoing randomized trials should address this issue.
Keywords: definition; heart failure; iron deficiency.
Copyright © 2022 The Authors. Published by Elsevier Inc. All rights reserved.
Conflict of interest statement
Funding Support and Author Disclosures Drs Pellicori and Cleland are supported by the British Heart Foundation Centre of Research Excellence (RE/18/6/34217). Dr Graham has received a sponsorship from Vifor to attend an international meeting. Dr Cleland has received personal fees from Abbott, Amgen, Novartis, Medtronic, Idorsia, Servier, AstraZeneca, Innolife, Torrent, and Respicardia; has received grants and personal fees from Bayer, Bristol Myers Squibb, Vifor, Pharmacosmos, Cytokinetics, Johnson & Johsnon, Myokardia, Stealth Biopharmaceuticals, and Viscardia; and has received personal fees and nonfinancial support from Boehringer Ingelheim, outside the submitted work. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose.
Comment in
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21st Century CE: The New Iron Age?J Am Coll Cardiol. 2022 Feb 1;79(4):352-354. doi: 10.1016/j.jacc.2021.11.026. J Am Coll Cardiol. 2022. PMID: 35086657 No abstract available.
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