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Galectin-3 and the Mineralocorticoid Receptor Antagonist Canrenone in Mild Heart Failure
Francesco Clemenza1, Serge Masson2, Pier Giulio Conaldi3
1Heart Failure Unit, ISMETT.
Insights
Galectin-3 (Gal-3) is a prognostic biomarker in heart failure. While Gal-3 levels increased over six months and correlated with outcomes, the mineralocorticoid receptor antagonist canrenone did not alter this association.
Area of Science:
- Cardiology
- Biomarkers
- Pharmacology
Background:
- Galectin-3 (Gal-3) is implicated in collagen deposition and inflammation.
- Gal-3 serves as a prognostic biomarker in heart failure (HF).
Purpose of the Study:
- To evaluate the treatment effect of canrenone on clinical outcomes in mild HF patients.
- To assess the association between Gal-3 levels, fibrosis markers, and clinical outcomes.
- To determine if baseline biomarker concentrations influence canrenone's effect on outcomes.
Main Methods:
- Serial measurement of Gal-3 and other fibrosis/cardiac stress markers in 413 mild HF patients.
- Randomization to either mineralocorticoid receptor antagonist canrenone or placebo.
- Correlation analysis between biomarkers, treatment, and clinical endpoints over 6 months.
Main Results:
- Gal-3 levels showed a slight increase over 6 months in both canrenone and placebo groups.
- Elevated Gal-3 levels were associated with adverse clinical endpoints.
- Canrenone's effect on clinical outcomes was independent of baseline Gal-3 or other fibrosis/stress markers.
Conclusions:
- Galectin-3 demonstrates prognostic value in mild heart failure.
- Canrenone treatment efficacy in mild HF is not modulated by baseline fibrosis or cardiac stress biomarkers.
- Further research may explore Gal-3's role in HF progression and therapeutic interventions.
Background:
Galectin-3 (Gal-3) is involved in collagen deposition and inflammation and is a prognostic biomarker in heart failure (HF).
Methods And Results:
Gal-3 and other markers of fibrosis or cardiac stress were measured serially in 413 patients with mild HF randomized to the mineralocorticoid receptor antagonist canrenone or placebo to evaluate treatment effect and association with clinical outcome. Gal-3 increased slightly over 6 months in both arms of the study and was associated with clinical endpoints.
Conclusions:
Although Gal-3 showed prognostic value, the effect of canrenone on clinical outcomes was unaffected by baseline concentrations of biomarkers of fibrosis or cardiac stress.
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