Abstract

Background: Heart failure with preserved ejection fraction (HFpEF) is increasingly recognized as a major global public health burden and lacks effective risk stratification. We aimed to assess a multi-biomarker model in improving risk prediction in HFpEF.Methods: We analyzed 18 biomarkers from the main pathophysiological domains of HF in 380 patients hospitalized for HFpEF from a prospective cohort. The association between these biomarkers and 2-year risk of all-cause death was assessed by Cox proportional hazards model. Support vector machine (SVM), a supervised machine learning method, was used to develop a prediction model of 2-year all-cause and cardiovascular death using a combination of 18 biomarkers and clinical indicators. The improvement of this model was evaluated by c-statistics, net reclassification improvement (NRI), and integrated discrimination improvement (IDI).Results: The median age of patients was 71-years, and 50.5% were female. Multiple biomarkers independently predicted the 2-year risk of death in Cox regression model, including N-terminal pro B-type brain-type natriuretic peptide (NT-proBNP), high-sensitivity cardiac troponin T (hs-TnT), growth differentiation factor-15 (GDF-15), tumor necrosis factor-α (TNFα), endoglin, and 3 biomarkers of extracellular matrix turnover [tissue inhibitor of metalloproteinases (TIMP)-1, matrix metalloproteinase (MMP)-2, and MMP-9) (FDR < 0.05). The SVM model effectively predicted the 2-year risk of all-cause death in patients with acute HFpEF in training set (AUC 0.834, 95% CI: 0.771–0.895) and validation set (AUC 0.798, 95% CI: 0.719–0.877). The NRI and IDI indicated that the SVM model significantly improved patient classification compared to the reference model in both sets (p < 0.05).Conclusions: Multiple circulating biomarkers coupled with an appropriate machine-learning method could effectively predict the risk of long-term mortality in patients with acute HFpEF. It is a promising strategy for improving risk stratification in HFpEF.

Highlights

  • Heart failure (HF) is a leading cardiovascular disorder with high morbidity and mortality [1]

  • Based on measurement of left ventricular ejection fraction (LVEF), HF is categorized into heart failure with reduced ejection fraction (HFrEF, LVEF

  • The guidelines of the European Society of Cardiology (ESC) [2] and the American Heart Association (AHA) [3] suggest that the incorporation of biomarkers with clinical and imaging tools can be beneficial for establishing the diagnosis and assessing disease severity in heart failure, including biomarkers of braintype natriuretic peptide (BNP), N-terminal pro-BNP (NTproBNP), and cardiac troponin

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Summary

Introduction

Heart failure (HF) is a leading cardiovascular disorder with high morbidity and mortality [1]. The guidelines of the European Society of Cardiology (ESC) [2] and the American Heart Association (AHA) [3] suggest that the incorporation of biomarkers with clinical and imaging tools can be beneficial for establishing the diagnosis and assessing disease severity in heart failure, including biomarkers of braintype natriuretic peptide (BNP), N-terminal pro-BNP (NTproBNP), and cardiac troponin. Other diagnostic biomarkers, such as soluble suppression of tumorigenicity 2 (sST2), galectin, and growth differentiation factor-15 (GDF-15), could be beneficial in guiding HF therapy. We aimed to assess a multi-biomarker model in improving risk prediction in HFpEF

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