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Prognostic value of galectin-3 and right ventricular function for long-term mortality in heart failure patients
Beata Zaborska1, Ewa Pilichowska-Paszkiet2, Ewa Makowska2
1Department of Cardiology, Centre of Postgraduate Medical Education, Grochowski Hospital, Grenadierów 51/59, 04-073, Warsaw, Poland. zaborska@kkcmkp.pl.
Insights
High galectin-3 levels and poor right ventricular (RV) function predict long-term mortality in heart failure (HF) patients receiving cardiac resynchronization therapy (CRT). Lack of CRT response further worsens survival in those with high galectin-3.
Area of Science:
- Cardiology
- Biomarkers
- Heart Failure Research
Background:
- Galectin-3 is associated with heart failure (HF) pathophysiology and right ventricular (RV) dysfunction.
- Cardiac resynchronization therapy (CRT) is a treatment for HF, but long-term prognostic factors require further investigation.
Purpose of the Study:
- To evaluate the long-term prognostic value of galectin-3 and RV function for all-cause mortality in HF patients undergoing CRT.
- To identify predictors of survival in patients with reduced left ventricular ejection fraction (LVEF) treated with CRT.
Main Methods:
- Prospective study of 63 symptomatic HF patients with LVEF ≤ 35% treated with CRT.
- Measurement of serum galectin-3 levels and comprehensive echocardiographic assessment of RV and left ventricular (LV) function.
- 5-year follow-up to determine all-cause mortality, analyzed using multivariable Cox regression.
Main Results:
- Baseline galectin-3 concentration and RV function (tricuspid annular plane systolic excursion) were independent predictors of 5-year all-cause mortality.
- High galectin-3 levels (HR 2.96) and impaired RV function (HR 0.88) were associated with increased mortality risk.
- Patients with high galectin-3 and poor response to CRT exhibited significantly lower survival rates.
Conclusions:
- Serum galectin-3 concentration and RV function are significant independent predictors of long-term mortality in heart failure with reduced ejection fraction (HFrEF) patients post-CRT.
- Galectin-3 may help identify HFrEF patients at higher risk of mortality, especially those with suboptimal response to CRT.
- These biomarkers offer potential for risk stratification and personalized treatment strategies in CRT recipients.
Abstract:
Recently, associations between the biomarker galectin-3 and numerous pathological processes involved in heart failure (HF) and right ventricular (RV) function have been observed. We aimed to assess the long-term prognostic ability of galectin-3 and RV function parameters for all-cause mortality in HF patients treated with cardiac resynchronization therapy (CRT). We prospectively studied 63 symptomatic HF patients with a left ventricular (LV) ejection fraction (EF) ≤ 35%. The median serum galectin-3 concentration was 13.4 ng/mL (IQR 11.05, 17.15). A detailed assessment of LV and RV geometry and function was performed with echocardiography. CRT defibrillator implantation was achieved in all patients without major complications. The follow-up lasted 5 years. In the multivariable Cox regression model, independent predictors for all-cause mortality were log baseline galectin-3 and baseline RV function expressed as tricuspid annular plane systolic excursion with HR 2.96 (p = 0.037) and HR 0.88 (p = 0.023), respectively. Analysis of subgroups defined by galectin-3 concentration and CRT response showed that patients with high baseline galectin-3 concentrations and a lack of response to CRT had a significantly lower probability of survival. In our patient cohort, the baseline galectin-3 concentration and RV function were independent predictors of long-term all-cause mortality in HFrEF patients following CRT implantation.
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