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Erythropoietin improves anemia exercise tolerance and renal function and reduces B-type natriuretic peptide and hospitalization in patients with heart failure and anemia - 18/08/11

Doi : 10.1016/j.ahj.2006.08.005 
Alberto Palazzuoli, MD, PhD a, , Donald Silverberg, MD b, Francesca Iovine, MD a, Stefano Capobianco, MD a, Giovanna Giannotti, MD a, Anna Calabrò, PhD a, Stella Maria Campagna, PhD a, Ranuccio Nuti, MD a
a Cardiology Section, Department of Internal Medicine and Metabolic Diseases, “Le Scotte” Hospital, University of Siena, Siena, Italy 
b Department of Nephrology, Tel Aviv Medical Center, Tel Aviv, Israel 

Reprint requests: Alberto Palazzuoli, MD, PhD, Department of Internal Medicine and Metabolic Diseases, University of Siena, “Le Scotte” Hospital, Viale Bracci, 53100 Siena, Italy.

Riassunto

Background

Anemia is now recognized as being a common finding in CHF and is associated with increased mortality and morbidity. However, it is uncertain whether the anemia is actually causing the worse prognosis or is merely a marker of more severe cardiac disease. Previous intervention studies with subcutaneous (sc) β-EPO in combination with iron have either been uncontrolled or case-controlled studies. We report a randomized, double-blind, placebo-controlled study of the combination of sc EPO and oral iron versus oral iron alone in patients with anemia and resistant CHF.

Objectives

The present study examines, in patients with advanced congestive heart failure (CHF) and anemia, the effects of β-erythropoietin (EPO) and oral iron on the anemia and on cardiac and renal functional parameters.

Methods

Forty consecutive subjects with moderate to severe CHF and anemia (hemoglobin [Hb] <11 g/dL) were studied. They were randomized to receive, in a double-blind fashion, either (a) (group A, the treatment group, 20 patients) sc β-EPO for 3 months twice weekly, in addition to daily oral iron, or (b) (group B, the placebo group, 20 patients) normal saline in sc injections and daily oral iron. Two patients in group B were eventually excluded because of a fall of Hb <8 g/dL requiring transfusion, leaving 18 patients in group B. After the 3-months study, the group A patients were maintained on the same treatment for an additional 9 months, whereas in Group B, the placebo and oral iron were stopped.

Results

In group A, after a mean of 3.5 ± 0.8 months of treatment, there was a significant increase in Hb from 10.4 ± 0.6 to 12.4 ± 0.8 g/dL (P < .01); a significant improvement in New York Heart Association functional class from 3.5 ± 0.6 to 2.8 ± 0.5 (P < .05); a longer endurance time on exercise testing, from 5.8 ± 2.2 to 7.8 ± 2.5 minutes (P < .01); a greater distance walked on exercise testing, from 278 ± 55 to 356 ± 88 meters (P < .01); a significant increase in the peak oxygen consumption (V·o2) from 12.8 ± 2.8 to 15.1 ± 2.8 mL/kg per minute (<.05); and the V·o2 at the anaerobic threshold, from 9.2 ± 2.0 to 13.2 ± 3.6 mL/kg minute (P < .01). There was also a significant fall in plasma B-type natriuretic peptide levels from 568 ± 320 to 271 ± 120 pg/mL (P < .01), a significant reduction in serum creatinine (P < .01), and an increase in estimated creatinine clearance (P < .05). In group B, there were no significant changes in any of the above parameters over the study period. At the end of the 1-year study, the Hb was still higher in group A than group B, and the rate of hospital admissions/patients over the year averaged 0.8 ± 0.2 in group A and 1.7 ± 0.8 in group B (P < .01).

Conclusions

In anemic CHF patients, correction of anemia with EPO and oral iron leads to improvement in New York Heart Association status, measured exercise endurance, oxygen use during exercise, renal function and plasma B-type natriuretic peptide levels and reduces the need for hospitalization.

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© 2006  Pubblicato da Elsevier Masson SAS.
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Vol 152 - N° 6

P. 1096.e9-1096.e15 - Dicembre 2006 Ritorno al numero
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