Research papers of the week – December 6, 2021

Michał Tkaczyszyn, Josep Comin-Colet, Adriaan A. Voors, Dirk J. van Veldhuisen, Cristina Enjuanes, Pedro Moliner, Marcin Drozd, Radosław Sierpiński, Piotr Rozentryt, Jolanta Nowak, Tomasz Suchocki, Waldemar Banasiak, Piotr Ponikowski, Peter van der Meer, Ewa A. Jankowska

European Journal of Heart Failure

Ministerial score = 200.0
JIF Impact Factor (2020) = 15.534 (Q1)

Aims: Abnormal endogenous erythropoietin (EPO) constitutes an important cause of anaemia in chronic diseases. We analysed the relationships between iron deficiency (ID) and the adequacy of endogenous EPO in anaemic heart failure (HF) patients, and the impact of abnormal EPO on 12-month mortality. Methods and results: We investigated 435 anaemic HF patients (age: 74 ± 10 years; males: 60%; New York Heart Association class I or II: 39%; left ventricular ejection fraction: 43 ± 17%). Patients with EPO higher than expected for a given haemoglobin were considered EPO-resistant whereas those with EPO lower than expected - EPO-deficient. ID was defined as serum ferritin <100 µg/L or 100–299 µg/L with transferrin saturation <20%. EPO-resistant patients (22%) had more advanced HF whereas those with EPO deficiency (57%) were more frequently females and had worse renal function. Lower serum ferritin (indicating depleted body iron stores) was related to higher EPO observed/predicted ratio when adjusted for significant clinical confounders, including C-reactive protein. One year all-cause mortality was 28% in patients with EPO resistance compared to 17% in patients with EPO deficiency and 10% in patients with adequate EPO (log-rank test for the comparison EPO resistance vs. adequate EPO: P = 0.02). When adjusted for other prognosticators, there was still a trend towards increased 12-month mortality in patients with higher EPO level. Conclusion: Anaemic HF patients with endogenous EPO deficiency vs. resistance have different clinical and laboratory characteristics. In such patients, ID contributes to EPO resistance independently of inflammation.

DOI:10.1002/ejhf.2253

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