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Galectin-3 as a marker for clinical prognosis and cardiac remodeling in acute heart failure
R I Lala1,2, D Lungeanu3, D Darabantiu4,5
1"Vasile Goldis" West University Arad, Arad, Romania. radu_lala@yahoo.com.
Insights
Galectin-3 is a significant predictor of mortality in patients with acute heart failure (AHF). Elevated galectin-3 levels correlate with left ventricular remodeling and worse survival outcomes in AHF patients.
Area of Science:
- Cardiology
- Biomarker Research
- Heart Failure Management
Background:
- Galectin-3 is implicated in heart failure (HF) development.
- Previous research focused on chronic HF, with limited data on acute HF (AHF).
- Understanding galectin-3's role in AHF is crucial for prognosis.
Purpose of the Study:
- To validate galectin-3 as a prognostic marker in AHF patients.
- To explore the relationship between galectin-3 levels and left ventricular (LV) remodeling in AHF.
Main Methods:
- A cohort of 69 hospitalized AHF patients was followed for 18 months.
- Galectin-3 and echocardiographic parameters were assessed at baseline and 6 months.
- Survival analysis and LV remodeling assessments were conducted.
Main Results:
- High baseline galectin-3 (>16.5 ng/ml) predicted worse 18-month survival (HR 4.66).
- Increasing galectin-3 levels over 6 months predicted short-term HF re-admission (HR 4.44).
- Galectin-3 levels correlated with pathological changes in LV relative wall thickness, end-diastolic diameter, and volume.
Conclusions:
- Galectin-3 serves as a reliable predictor of long-term mortality in AHF.
- Increasing galectin-3 levels are associated with left ventricular remodeling in AHF.
Background:
Galectin-3 has been reported as a mediator of heart failure (HF) development and progression. Most studies, however, have been conducted on patients with chronic HF rather than acute HF (AHF). The aim of this study was to confirm galectin-3 as a prognostic marker in subjects with AHF and to investigate its possible relationship with left ventricular (LV) remodeling.
Methods:
A total of 69 patients hospitalized with a primary diagnosis of AHF were followed up for 18 months. Galectin-3 and echocardiographic parameters were measured at baseline and after 6 months. Survival analysis and exploratory analysis of LV remodeling were performed.
Results:
Patients with high baseline galectin-3 values (>16.5 ng/ml) had a significantly worse survival profile over the 18-month follow-up (log-rank test, p = 0.017), with Cox proportional hazards modeling showing a crude hazard ratio (HR) of 4.66 (95% CI = 1.16-18.67; likelihood-ratio test, p = 0.037) for all-cause mortality. Changes in galectin-3 levels (1 SD increase over 6 months) proved to be a significant explanatory factor for HF hospital re-admission in the short term when compared with quasi-stationary galectin-3 levels: worse Kaplan-Meier survival curves (log-rank test, p = 0.001) and a crude HR of 4.44 (95% CI = 1.76-11.18; likelihood-ratio test, p = 0.004). A significant association was found between the pathological evolution of relative wall thickness, LV end-diastolic diameter, LV end-diastolic volume, and increasing levels of galectin-3 in the short term (Cochran-Mantel-Haenszel test, p < 0.01).
Conclusion:
Galectin-3 can predict long-term mortality in patients with AHF. The results of our study suggest a possible relation between left ventricular remodeling and increasing galectin-3 levels.
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