Redefining Iron Deficiency in Patients With Chronic Heart Failure

Author:

Packer Milton12ORCID,Anker Stefan D.3ORCID,Butler Javed415ORCID,Cleland John G.F.6ORCID,Kalra Paul R.789,Mentz Robert J.1011ORCID,Ponikowski Piotr1213ORCID,Talha Khawaja M.5ORCID

Affiliation:

1. Baylor University Medical Center (M.P.), Dallas, TX.

2. Imperial College, London, UK (M.P.).

3. Department of Cardiology, German Heart Center Charité, Institute of Health Center for Regenerative Therapies, German Centre for Cardiovascular Research, partner site Berlin, Charité Universitätsmedizin, Berlin, Germany (S.D.A.).

4. Baylor Scott and White Research Institute (J.B.), Dallas, TX.

5. University of Mississippi Medical Center, Jackson (J.B., K.M.T.).

6. British Heart Foundation Centre of Research Excellence, School of Cardiovascular and Metabolic Health (J.G.F.C.), University of Glasgow, UK.

7. College of Medical, Veterinary & Life Sciences (P.R.K.), University of Glasgow, UK.

8. Department of Cardiology, Portsmouth Hospitals University NHS Trust, Portsmouth, UK (P.R.K.).

9. Faculty of Science and Health, University of Portsmouth, UK (P.R.K.).

10. Division of Cardiology, Department of Medicine, Duke University School of Medicine, Durham, NC (R.J.M.).

11. Duke Clinical Research Institute, Durham, NC (R.J.M.).

12. Institute of Heart Diseases, Wroclaw Medical University, Poland (P.P.).

13. Institute of Heart Diseases, University Hospital, Wroclaw, Poland (P.P.).

Abstract

A serum ferritin level <15 to 20 μg/L historically identified patients who had absent bone marrow iron stores, but serum ferritin levels are distorted by the systemic inflammatory states seen in patients with chronic kidney disease or heart failure. As a result, nearly 25 years ago, the diagnostic ferritin threshold was increased 5- to 20-fold in patients with chronic kidney disease (ie, iron deficiency was identified if the serum ferritin level was <100 μg/L, regardless of transferrin saturation [TSAT], or 100 to 299 μg/L if TSAT was <20%). This guidance was motivated not by the findings of studies of total body or tissue iron depletion, but by a desire to encourage the use of iron supplements to potentiate the response to erythropoiesis-stimulating agents in patients with renal anemia. However, in patients with heart failure, this definition does not reliably identify patients with an absolute or functional iron-deficiency state, and it includes individuals with TSATs (≥20%) and serum ferritin levels in the normal range (20–100 mg/L) who are not iron deficient, have an excellent prognosis, and do not respond favorably to iron therapy. Furthermore, serum ferritin levels may be distorted by the use of both neprilysin and sodium-glucose cotransporter 2 inhibitors, both of which may act to mobilize endogenous iron stores. The most evidence-based and trial-tested definition of iron deficiency is the presence of hypoferremia, as reflected by as a TSAT <20%. These hypoferremic patients are generally iron deficient on bone marrow examination, and after intravenous iron therapy, they exhibit an improvement in exercise tolerance and functional capacity (when meaningfully impaired) and show the most marked reduction (ie, 20%–30%) in the risk of cardiovascular death or total heart failure hospitalizations. Therefore, we propose that the current ferritin-driven definition of iron deficiency in heart failure should be abandoned and that a definition based on hypoferremia (TSAT <20%) should be adopted.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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