Key result
Optimizing guideline-directed medical therapy in elderly HFimpEF linked to broadly improved multi-organ biomarker profiles.
Why the study?
The study aimed to evaluate circulating biomarker levels in elderly patients with improved heart failure ejection fraction, previously with LVEF <40%, after six months of drug therapy optimisation.
Does therapeutic optimisation over six months improve circulating cardiovascular biomarkers and echocardiographic parameters in elderly patients with HFimpEF?
Observational (n=100)
No
Does therapeutic optimisation over six months improve circulating cardiovascular biomarkers and echocardiographic parameters in elderly patients with HFimpEF?
p-value: p=<0.001
Guideline-directed medical therapy optimization over six months in patients with HFimpEF yields significant structural and multi-system functional benefits, validated by improved echocardiographic indices and favorable reductions in inflammatory and oxidative stress biomarkers.
Should not yet change practice in elderly HFimpEF; hypothesis-generating for GDMT biomarker effects.
Background: Heart failure (HF) is a clinical syndrome that involves multiple interconnected pathways. Circulating biomarkers in HF emerged as powerful tools for risk stratification, diagnostic confirmation, prognostic assessment, and monitoring of treatment efficacy. The aim of the present study was to evaluate circulating levels of biomarkers in elderly patients with improved HF ejection fraction, previously with left ventricular ejection fraction (LVEF) <40%, after six months of drug therapy optimisation. Methods: We enrolled 100 HFimpEF outpatients. All patients provided medical history and underwent physical examination at baseline and after six months of follow-up. The serum values of circulating biomarkers were assessed with an ELISA test. Proteomic analysis was performed on serum samples collected from a subset of 13 patients at baseline and after six months of follow-up. Results: At follow-up, we observed significant improvements in glycometabolic, renal and inflammatory profiles (p < 0.001). Proteomic analysis revealed selective changes in key cardiovascular (CV)-related proteins, such as insulin-like growth factor-binding protein 4 (IBP4), thrombospondin-4 (TSP4), intercellular adhesion molecule 1 (ICAM1), and syndecan-4 (SDC4). Conclusions: This study demonstrates significant improvements across multiple CV biomarkers after six months of therapy optimisation in HFimpEF patients, providing evidence for comprehensive therapeutic effects targeting inflammation, oxidative stress, neurohormonal activation, and thrombotic risk.
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Cassano et al. (2026) conducted an observational in Heart failure with improved ejection fraction (HFimpEF) (n=100). Drug therapy optimization was evaluated on Glycometabolic, renal and inflammatory profiles (p=<0.001). Six months of drug therapy optimization in elderly patients with HFimpEF significantly improved glycometabolic, renal, and inflammatory biomarker profiles.
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