Abstract | AIMS: Anaemia is often observed in patients with chronic heart failure (CHF), and it may be associated with a worse prognosis. Aim of this study was to identify the individual mechanisms of anaemia in CHF patients. METHODS AND RESULTS: One hundred and forty-eight consecutive patients with haemoglobin concentration <13 g/dL (if males) or <12 g/dL (if females) were enrolled. Factors responsible for anaemia were investigated by evaluating endogenous erythropoietin (Epo) production, serum cytokines levels, body iron status, and iron supply for erythropoiesis. Most patients (57%) presented anaemia of chronic disease and among them, 92% showed evidence of a defective endogenous Epo production. This was indicated by an observed/predicted log(serum Epo) ratio less than 0.8 and/or a defective iron supply for erythropoiesis diagnosed by low transferrin saturation and/or increased value of soluble transferrin receptor. According to regression analysis sex, renal failure, and serum Epo were correlated with anaemia. CONCLUSION: According to our study, about half of anaemic CHF patients showed anaemia of chronic disease with blunted endogenous Epo production and/or a defective iron supply for erythropoiesis. Determination of the individual mechanisms of anaemia in CHF could justify a rational therapeutic approach to anaemia.
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Authors | Cristina Opasich, Mario Cazzola, Laura Scelsi, Stefania De Feo, Enzo Bosimini, Rocco Lagioia, Oreste Febo, Roberto Ferrari, Alessandro Fucili, Remigio Moratti, Roberto Tramarin, Luigi Tavazzi |
Journal | European heart journal
(Eur Heart J)
Vol. 26
Issue 21
Pg. 2232-7
(Nov 2005)
ISSN: 0195-668X [Print] England |
PMID | 15987710
(Publication Type: Journal Article, Multicenter Study, Research Support, Non-U.S. Gov't)
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Chemical References |
- Cytokines
- Receptors, Transferrin
- Erythropoietin
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Topics |
- Anemia
(etiology)
- Chronic Disease
- Cytokines
(metabolism)
- Erythropoiesis
(physiology)
- Erythropoietin
(deficiency)
- Female
- Heart Failure
(blood, complications)
- Humans
- Iron Deficiencies
- Male
- Middle Aged
- Receptors, Transferrin
(metabolism)
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