| Literature DB >> 30957868 |
Filippos Triposkiadis1, Javed Butler2, Francois M Abboud3, Paul W Armstrong4, Stamatis Adamopoulos5, John J Atherton6, Johannes Backs7, Johann Bauersachs8, Daniel Burkhoff9, Robert O Bonow10, Vijay K Chopra11, Rudolf A de Boer12, Leon de Windt13, Nazha Hamdani14, Gerd Hasenfuss15, Stephane Heymans16, Jean-Sébastien Hulot17,18,19, Marvin Konstam20, Richard T Lee21, Wolfgang A Linke22, Ida G Lunde23, Alexander R Lyon24,25, Christoph Maack26, Douglas L Mann27, Alexandre Mebazaa28, Robert J Mentz29, Petros Nihoyannopoulos30, Zoltan Papp31, John Parissis32, Thierry Pedrazzini33, Giuseppe Rosano34, Jean Rouleau35, Petar M Seferovic36, Ajay M Shah37, Randall C Starling38, Carlo G Tocchetti39, Jean-Noel Trochu40, Thomas Thum41, Faiez Zannad42, Dirk L Brutsaert43, Vincent F Segers44,45, Gilles W De Keulenaer44,46.
Abstract
Randomized clinical trials initially used heart failure (HF) patients with low left ventricular ejection fraction (LVEF) to select study populations with high risk to enhance statistical power. However, this use of LVEF in clinical trials has led to oversimplification of the scientific view of a complex syndrome. Descriptive terms such as 'HFrEF' (HF with reduced LVEF), 'HFpEF' (HF with preserved LVEF), and more recently 'HFmrEF' (HF with mid-range LVEF), assigned on arbitrary LVEF cut-off points, have gradually arisen as separate diseases, implying distinct pathophysiologies. In this article, based on pathophysiological reasoning, we challenge the paradigm of classifying HF according to LVEF. Instead, we propose that HF is a heterogeneous syndrome in which disease progression is associated with a dynamic evolution of functional and structural changes leading to unique disease trajectories creating a spectrum of phenotypes with overlapping and distinct characteristics. Moreover, we argue that by recognizing the spectral nature of the disease a novel stratification will arise from new technologies and scientific insights that will shape the design of future trials based on deeper understanding beyond the LVEF construct alone. Published on behalf of the European Society of Cardiology. All rights reserved.Entities:
Keywords: Ejection fraction; Endothelium; Heart failure; Pathophysiology
Mesh:
Year: 2019 PMID: 30957868 DOI: 10.1093/eurheartj/ehz158
Source DB: PubMed Journal: Eur Heart J ISSN: 0195-668X Impact factor: 29.983