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Published on: January 28, 2020
Biomarkers in heart failure
Manuel Garofalo1, Giorgia Panichella1, Alberto Aimo2
1Department of Clinical and Experimental Medicine, University of Florence, Florence, Italy; Cardiomyopathy Unit, Careggi University Hospital, Florence, Italy.
Insights
Biomarkers are crucial for managing heart failure (HF), aiding diagnosis and prognosis. Novel biomarkers and AI integration promise personalized HF care, moving beyond traditional approaches for better patient outcomes.
Area of Science:
- Cardiology and Clinical Biomarker Research
- Translational Medicine and Precision Health
Background:
- Heart failure (HF) is a major global health burden with complex pathophysiology.
- Circulating biomarkers are vital for HF diagnosis, prognosis, and treatment guidance.
- Established biomarkers like BNP/NT-proBNP have limitations, necessitating research into novel markers.
Purpose of the Study:
- To review the evolving role of circulating biomarkers in heart failure management.
- To highlight established and emerging biomarkers and their pathophysiological relevance.
- To discuss the future potential of multimarker strategies and AI in personalized HF care.
Main Methods:
- Review of current literature on established and novel biomarkers in HF.
- Analysis of biomarker utility in diagnosis, prognostication, and therapeutic guidance.
- Exploration of emerging technologies like omics and AI for biomarker integration.
Main Results:
- BNP/NT-proBNP are cornerstones but influenced by clinical factors.
- Cardiac troponins and hsCRP offer prognostic insights into myocardial injury and inflammation.
- Novel biomarkers (Gal-3, sST2, GDF-15, MPO, MR-proADM) and non-coding RNAs provide incremental value.
- Multimarker strategies and AI show promise for refined risk stratification.
Conclusions:
- Biomarkers are essential pillars in modern heart failure care.
- Emerging biomarkers and advanced technologies are transforming HF management.
- The future of HF care lies in personalized, biomarker-guided strategies.
Abstract:
Heart failure (HF) is a leading cause of morbidity and mortality worldwide, characterized by a complex pathophysiology and heterogeneous clinical trajectories. Circulating biomarkers have progressively moved from ancillary diagnostic tools to indispensable instruments that inform diagnosis, prognostication, and therapeutic guidance. B-type natriuretic peptide (BNP) and N-terminal pro-B-type natriuretic peptide (NT-proBNP) remain the cornerstones of biomarker-guided management, yet their interpretation is influenced by age, renal function, obesity, and atrial fibrillation. Cardiac troponins, originally validated for myocardial infarction, provide robust prognostic information in both acute and chronic HF by reflecting ongoing myocardial injury, while high-sensitivity C-reactive protein (hsCRP) captures systemic inflammation and its impact on outcomes. The scope of biomarker research has rapidly expanded to novel pathways. Galectin-3 (Gal-3) and soluble suppression of tumorigenicity-2 (sST2) are established mediators of fibrosis and remodeling, offering incremental prognostic value beyond natriuretic peptides. Growth differentiation factor-15 (GDF-15), myeloperoxidase (MPO), and mid-regional pro-adrenomedullin (MR-proADM) integrate systemic stress, congestion, and oxidative injury into risk assessment. More recently, non-coding RNAs-including microRNAs (miRNAs) and long non-coding RNAs (lncRNAs)-have emerged as minimally invasive, pathophysiologically grounded biomarkers with diagnostic, prognostic, and even therapeutic implications. Looking ahead, multimarker strategies that combine complementary pathways provide a multidimensional perspective on HF progression and therapeutic response. Advances in high-throughput omics platforms and artificial intelligence (AI) promise to refine biomarker integration into precision medicine, enabling individualized risk stratification and therapy optimization. Altogether, biomarkers now represent essential pillars of modern HF care and hold the potential to transform management from population-based to personalized strategies.
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