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Galectin-3 Beyond Conventional Cardiac Biomarkers and Its Incremental Prognostic Value in Heart Failure: A Systematic
Vaishnavi Hemdev1, Anushka Rani2, Ahsan Qadeer3
1Internal Medicine, University of York, York, GBR.
Insights
Galectin-3 shows promise in predicting heart failure outcomes, especially in specific patient groups. Serial measurements of this fibrosis biomarker offer greater prognostic insight than single assessments.
Area of Science:
- Cardiology
- Biomarker Research
- Clinical Medicine
Background:
- Accurate risk stratification in heart failure (HF) is challenging despite current biomarkers.
- Galectin-3, a marker of inflammation and fibrosis, is a potential prognostic indicator.
- Its added value beyond established cardiac biomarkers needs further definition.
Purpose of the Study:
- To systematically review evidence on the prognostic role of galectin-3 in adult HF.
- To assess the incremental value of galectin-3 beyond conventional biomarkers.
- To explore its utility in different HF phenotypes and disease stages.
Main Methods:
- Systematic review of seven high-quality primary studies.
- Inclusion of diverse HF populations: community, ambulatory, HFpEF, acute decompensated, post-discharge.
- Focus on studies evaluating galectin-3's prognostic impact and additive value.
Main Results:
- Galectin-3 demonstrated incremental prognostic value for mortality and HF hospitalization.
- This was particularly evident in fibrosis-dominant phenotypes like HFpEF and acute decompensated HF.
- Prognostic utility was reduced in well-treated chronic HF with reduced ejection fraction after natriuretic peptide adjustment.
- Serial galectin-3 measurements showed stronger associations with adverse outcomes than single assessments.
Conclusions:
- Galectin-3 plays a phenotype-specific and dynamic role in HF prognosis.
- It reflects myocardial remodeling, not solely hemodynamic stress.
- Findings support galectin-3's utility in risk stratification and disease monitoring for specific HF types.
- Further prospective studies are needed to guide management strategies using galectin-3.
Abstract:
Heart failure is a heterogeneous clinical syndrome in which accurate risk stratification remains challenging despite the widespread use of natriuretic peptides and cardiac troponins. Galectin-3, a biomarker of inflammation and myocardial fibrosis, has emerged as a potential complementary prognostic marker; however, its incremental value beyond established biomarkers remains incompletely defined. This systematic review synthesizes primary clinical evidence evaluating the prognostic role of galectin-3 in adult heart failure populations, with a specific focus on its additive value beyond conventional cardiac biomarkers. A comprehensive literature search identified seven high-quality primary studies encompassing community-based cohorts, ambulatory chronic heart failure, heart failure with preserved ejection fraction, acute decompensated heart failure, and post-discharge populations. Across these studies, galectin-3 demonstrated incremental prognostic value for adverse outcomes, including mortality and heart failure-related hospitalization, particularly in fibrosis-dominant phenotypes such as heart failure with preserved ejection fraction and acute or recently decompensated heart failure. In contrast, its prognostic utility was attenuated in well-treated ambulatory patients with chronic heart failure with reduced ejection fraction after adjustment for natriuretic peptides. Importantly, studies incorporating serial galectin-3 measurements consistently demonstrated stronger associations with adverse outcomes than single baseline assessments, highlighting the value of longitudinal biomarker evaluation. Overall, the available evidence supports a phenotype-specific and dynamic role for galectin-3 as a complementary prognostic biomarker that reflects myocardial remodeling rather than hemodynamic stress alone. These findings refine the clinical positioning of galectin-3 and underscore its potential utility in risk stratification and disease monitoring, while emphasizing the need for prospective studies to evaluate galectin-3-guided management strategies.
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