PMID- 20570952 OWN - NLM STAT- MEDLINE DCOM- 20110728 LR - 20220330 IS - 1522-9645 (Electronic) IS - 0195-668X (Linking) VI - 31 IP - 15 DP - 2010 Aug TI - Iron deficiency: an ominous sign in patients with systolic chronic heart failure. PG - 1872-80 LID - 10.1093/eurheartj/ehq158 [doi] AB - AIMS: Beyond erythropoiesis, iron is involved in numerous biological processes crucial for maintenance of homeostasis. Patients with chronic heart failure (CHF) are prone to develop iron deficiency (ID), and iron supplementation improves their functional status and quality of life. We sought to examine the relationship between ID and survival in patients with systolic CHF. METHODS AND RESULTS: In a prospective observational study, we evaluated 546 patients with stable systolic CHF [age: 55 +/- 11 (mean +/- standard deviation) years, males: 88%, left ventricular ejection fraction: 26 +/- 7%, New York Heart Association (NYHA) class (I/II/III/IV): 57/221/226/42]. Iron deficiency was defined as: ferritin <100 microg/L, or 100-300 microg/L with transferrin saturation <20%. The prevalence of ID was 37 +/- 4% [+/-95% confidence intervals (CI)] in the entire CHF population (32 +/- 4 vs. 57 +/- 10%-in subjects without vs. with anaemia defined as haemoglobin level <12 g/dL in women and <13 g/dL in men, P < 0.001). In a multiple logistic model, ID was more prevalent in women, those in the advanced NYHA class, with higher plasma N-terminal pro-type B natriuretic peptide and higher serum high-sensitivity C-reactive protein (all P < 0.05). At the end of follow-up (mean duration: 731 +/- 350 days), there were 153 (28%) deaths and 30 (6%) heart transplantations (HTX). In multivariable models, ID (but not anaemia) was related to an increased risk of death or HTX (adjusted hazard ratio 1.58, 95% CI 1.14-2.17, P < 0.01). CONCLUSION: In patients with systolic CHF, ID is common and constitutes a strong, independent predictor of unfavourable outcome. Iron supplementation may be considered as a therapeutic approach in these patients to improve prognosis. FAU - Jankowska, Ewa A AU - Jankowska EA AD - Department of Heart Diseases, Wroclaw Medical University, Centre for Heart Diseases, Military Hospital, ul. Weigla 5, Wroclaw, Poland. ewa.jankowska@antro.pan.wroc.pl FAU - Rozentryt, Piotr AU - Rozentryt P FAU - Witkowska, Agnieszka AU - Witkowska A FAU - Nowak, Jolanta AU - Nowak J FAU - Hartmann, Oliver AU - Hartmann O FAU - Ponikowska, Beata AU - Ponikowska B FAU - Borodulin-Nadzieja, Ludmila AU - Borodulin-Nadzieja L FAU - Banasiak, Waldemar AU - Banasiak W FAU - Polonski, Lech AU - Polonski L FAU - Filippatos, Gerasimos AU - Filippatos G FAU - McMurray, John J V AU - McMurray JJ FAU - Anker, Stefan D AU - Anker SD FAU - Ponikowski, Piotr AU - Ponikowski P LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20100621 PL - England TA - Eur Heart J JT - European heart journal JID - 8006263 RN - 0 (Peptide Fragments) RN - 0 (Transferrin) RN - 0 (pro-brain natriuretic peptide (1-76)) RN - 114471-18-0 (Natriuretic Peptide, Brain) RN - 9007-41-4 (C-Reactive Protein) RN - 9007-73-2 (Ferritins) SB - IM EIN - Eur Heart J. 2011 May;32(9):1054 MH - Aged MH - C-Reactive Protein/metabolism MH - Chronic Disease MH - Disease-Free Survival MH - Female MH - Ferritins/blood MH - Heart Failure, Systolic/*complications/metabolism MH - Humans MH - *Iron Deficiencies MH - Kaplan-Meier Estimate MH - Male MH - Middle Aged MH - Natriuretic Peptide, Brain/metabolism MH - Peptide Fragments/metabolism MH - Prognosis MH - Prospective Studies MH - Transferrin/metabolism EDAT- 2010/06/24 06:00 MHDA- 2011/07/29 06:00 CRDT- 2010/06/24 06:00 PHST- 2010/06/24 06:00 [entrez] PHST- 2010/06/24 06:00 [pubmed] PHST- 2011/07/29 06:00 [medline] AID - ehq158 [pii] AID - 10.1093/eurheartj/ehq158 [doi] PST - ppublish SO - Eur Heart J. 2010 Aug;31(15):1872-80. doi: 10.1093/eurheartj/ehq158. Epub 2010 Jun 21.