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ABSTRACT: Background
There is a growing recognition of the inherent limitations of the use of the left ventricular ejection fraction (LVEF) to accurately phenotype patients with heart failure (HF).Objectives
The authors sought to identify unique proteomic signatures for patients with HF with reduced ejection fraction (HFrEF), HF with a midrange LVEF (HFmrEF), and HF with preserved ejection fraction (HFpEF), as well as to identify molecular differences between patients with ischemic and nonischemic HF.Methods
We used high-content aptamer-based proteomics technology (SOMAscan) to interrogate the blood proteome of age- and sex-matched patients with HF within different LVEF groups.Results
Within the Washington University Heart Failure Registry, we identified age/sex-match
SUBMITTER: Adamo L
PROVIDER: S-EPMC7584807 | biostudies-literature | 2020 Oct
REPOSITORIES: biostudies-literature