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Published on: July 14, 2021
Galectin-3 as a Predictor of Left Ventricular Reverse Remodeling in Recent-Onset Dilated Cardiomyopathy
Konstantinos Karatolios1, Georgios Chatzis1, Volker Holzendorf2
1Department of Cardiology, Angiology and Intensive Care, Philipps University Marburg, Marburg, Germany.
Insights
Low galectin-3 levels predict favorable left ventricular reverse remodeling (LVRR) in recent-onset dilated cardiomyopathy (RODCM) patients. This biomarker indicates positive ventricular remodeling, aiding clinical decisions.
Area of Science:
- Cardiology
- Biomarkers
- Heart Failure Research
Background:
- Galectin-3's association with heart failure outcomes is known.
- Limited data exists on galectin-3's predictive value for left ventricular reverse remodeling (LVRR) in recent-onset dilated cardiomyopathy (RODCM).
Purpose of the Study:
- To investigate the clinical usefulness and predictive value of galectin-3 for LVRR in RODCM patients.
- To determine if baseline galectin-3 levels can predict favorable ventricular remodeling.
Main Methods:
- 57 RODCM patients were assessed for baseline galectin-3 levels.
- LVRR was defined by echocardiographic improvements in ejection fraction and left ventricular end-diastolic diameter at 12 months.
- Receiver operating characteristic analysis identified an optimal galectin-3 cutoff of 59 ng/ml.
Main Results:
- 66% of patients achieved LVRR within 12 months.
- Univariate analysis showed NYHA functional class and baseline galectin-3 levels were associated with LVRR.
- Galectin-3 remained an independent predictor of LVRR after covariate adjustment.
Conclusions:
- Baseline galectin-3 is an independent predictor of LVRR in RODCM.
- Low galectin-3 levels serve as a useful biomarker for favorable ventricular remodeling in this patient group.
Objectives:
Studies have evaluated the association of galectin-3 and outcome in patients with heart failure. However, there is still scarce evidence concerning the clinical usefulness and predictive value of galectin-3 for left ventricular reverse remodeling (LVRR) in patients with recent-onset dilated cardiomyopathy (RODCM).
Patients And Methods:
Baseline galectin-3 was measured in 57 patients with RODCM. All patients were followed for at least 12 months. The study end point was LVRR at 12 months, defined as an absolute improvement of the left ventricular ejection fraction of ≥10% to a final value of ≥35%, accompanied by a decrease in the left ventricular end diastolic diameter of at least 10%, as assessed by echocardiography. In receiver operating characteristic curve analysis, the optimum cut-off value for baseline galectin-3 with the highest Youden index was 59 ng/ml.
Results:
Overall, LVRR at 12 months was observed in 38 patients (66%). In a univariate analysis, NYHA functional class and baseline galectin-3 levels were associated with LVRR. After adjustment for covariates, galectin-3 remained an independent predictor for LVRR.
Conclusions:
Our study suggests that baseline galectin-3 is an independent predictor of LVRR. Low levels of galectin-3 may be regarded a useful biomarker of favorable ventricular remodeling in patients with RODCM.
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