Key result
Elevated suPAR linked to ~60% increase in acute decompensated heart failure.
Why the study?
Existing biomarkers for HF lack specificity, prompting evaluation of suPAR, H-FABP, VCAM-1, and GDF-15 to distinguish acute decompensated from compensated stable HF.
Do novel biomarkers (suPAR, GDF-15, VCAM-1, H-FABP) improve the detection and prediction of acute decompensated heart failure compared to stable compensated heart failure?
Cross-Sectional (n=146)
No
Do novel biomarkers (suPAR, GDF-15, VCAM-1, H-FABP) improve the detection and prediction of acute decompensated heart failure compared to stable compensated heart failure?
Effect estimate: 1.6-fold-change
p-value: p=<0.0001
Novel biomarkers like suPAR and VCAM-1 demonstrate high predictive accuracy for detecting acute decompensated heart failure, potentially offering a more specific diagnostic tool than NT-proBNP.
Background/Objectives: Heart failure (HF) remains a major therapeutic and diagnostic challenge nowadays. Albeit, acute decompensated HF is associated with several clinical signs such as dyspnea or edema, it remains a challenge to use easy accessible and suitable tools, such as biomarkers, to distinguish between patients at risk for an acute decompensation of their heart failure and compensated, stable HF patients. Existing biomarkers, such as natriuretic peptides or troponin, are not specific and can be elevated due to several other disease conditions, such as myocardial infarction, atrial fibrillation, or valve diseases. Therefore, the aim of this study was to analyze the predictive potential of four novel cardiovascular biomarkers—the soluble urokinase-type plasminogen activator receptor (suPAR), heart-type fatty acid binding protein (H-FABP), vascular cell adhesion molecule 1 (VCAM-1), and growth/differentiation factor 15 (GDF-15) for the detection of cardiac decompensation in patients with HF. Methods: In this study, 146 patients were prospectively enrolled and the serum biomarker concentrations were analyzed using Enzyme Linked Immunosorbent Assay (ELISA). We correlated the biomarker concentrations with clinical and biochemical parameters of all patients and the predictive value for detection of cardiac decompensation was assessed. Results: A significant increase in the levels of suPAR (1.6-fold-change, p < 0.0001), H-FABP (2.2-fold-change, p = 0.0458), VCAM-1 (1.6-fold-change, p < 0.0001), and GDF-15 (1.7-fold-change, p = 0.0009) was detected in all patients with acute decompensated HF in comparison to patients with compensated HF. Univariate logistic regression analysis revealed a significant association of biomarker plasma concentration with the risk for a cardiac decompensation (suPAR: p < 0.0001; VCAM-1: p < 0.0001, H-FABP: p = 0.0458; GDF-15: p = 0.0009). Conclusions: In conclusion, the investigated novel cardiovascular biomarkers suPAR, GDF-15, VCAM-1, and H-FABP could be a valuable tool to facilitate therapeutic decisions in patients with heart failure and suspicion of a cardiac decompensation. Parameters such as renal function should be taken into account. Further studies on novel biomarkers are required to find reliable, sensitive, and specific tools that will enable the early detection of patients with acute decompensation.
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Fröhling et al. (2024) conducted a cross-sectional in Heart failure (compensated and acute decompensated) (n=146). Acute decompensated heart failure vs. Compensated heart failure was evaluated on Increase in suPAR biomarker levels associated with acute decompensated heart failure (1.6-fold-change, p=<0.0001). The biomarkers suPAR and VCAM-1 were significantly elevated by 1.6-fold (p<0.0001) in patients with acute decompensated heart failure and demonstrated an AUC of 0.838 for predicting decompensation.
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