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Galectin-3 in Patients with Acute Heart Failure: Preliminary Report on First Polish Experience
Grażyna Sygitowicz1, Mariusz Tomaniak2, Krzysztof J Filipiak2
1Department of Laboratory Medical Diagnostics, Medical University of Warsaw, Poland.
Insights
Higher levels of Galectin-3 (Gal-3) in acute heart failure (AHF) patients indicate fibrosis and predict mortality. This novel serum marker shows promise for diagnosing AHF and assessing patient outcomes.
Area of Science:
- Cardiology
- Biomarker Discovery
- Heart Failure Research
Background:
- Galectin-3 (Gal-3) is implicated in heart failure (HF) progression, serving as a biomarker for fibrosis and inflammation.
- Elevated Gal-3 levels may predict increased morbidity and mortality in patients with heart failure.
Purpose of the Study:
- To investigate the diagnostic utility of a novel serum marker, Galectin-3, for acute heart failure (AHF).
- To assess the correlation between Gal-3 levels and other established biomarkers and clinical parameters in AHF patients.
Main Methods:
- Serum concentrations of Galectin-3 (Gal-3), NT-proBNP, and hsCRP were measured in 14 AHF patients and 19 healthy controls.
- Clinical parameters including left ventricular ejection fraction (LVEF) and prevalence of dyspnea were assessed.
- Survival rates were evaluated after a 12-month follow-up period.
Main Results:
- AHF patients exhibited significantly higher median Gal-3 concentrations (17.8 ng/mL) compared to controls (8.4 ng/mL) (p = 0.0007).
- A significant positive correlation was found between Gal-3 and NT-proBNP levels (Rs = 0.565; p = 0.035).
- Elevated Gal-3 levels were observed in AHF patients who died within 12 months (55.6 ng/mL) versus those who survived (15.0 ng/mL) (p = 0.005).
Conclusions:
- Increased Galectin-3 expression is indicative of myocardial fibrosis and remodeling in decompensated heart failure.
- Galectin-3 represents a valuable and promising serum biomarker for the diagnosis and prognosis of acute heart failure.
Background:
Galectin-3 (Gal-3) as a biomarker of fibrosis and inflammation has been implicated in the development and progression of heart failure (HF) and may predict increased morbidity and mortality in society.
Objectives:
In this preliminary report we investigated the utility of a novel serum marker for the diagnosis of acute HF (AHF).
Material And Methods:
The study involved 14 AHF patients aged 67.0 ± 14.6 yrs. with left ventricular ejection fraction (LVEF) 29.29 ± 10.73%, hospitalized at the Intensive Coronary Care Unit, where the research took place. In addition, a control group consisting of 19 volunteers who were age, gender and ethnically matched to the HF group was recruited. In the study group, the concentrations of Gal-3, NT-proBNP, hsCRP and basic clinical parameters, such as prevalence of dyspnea and LVEF were determined. The concentration of Gal-3 in serum was examined by an automated quantitative test (VIDAS® Galectin-3, bioMerieux SA, France) using the ELFA technique. The survival rate was assessed after a 12-month follow-up.
Results:
The median (IQR) Gal-3 concentrations in patients with AHF were higher (nearly 2.1-times) than in the control group - 17.8 (10.3-27.8) ng/mL vs. 8.4 (6.5-11.0) ng/mL; p = 0.0007. In our study group, the median (IQR) of concentrations of NT-proBNP 4723 (1415-29725) pg/mL and hsCRP 10.0 (4.9-13.9) mg/L were observed. In those patients, the statistically significant correlation (Spearman's rank-correlation coefficient) between the concentrations of Gal-3 and NT-proBNP (Rs = 0.565; p = 0.035) as well as the value of LVEF and the concentration of hsCRP (Rs = -0.663; p = 0.020) were stated. The serum Gal-3 concentrations were significantly higher among the 4 HF patients (28.6%) who had died than among the HF patients who were alive after this time (n = 10) (55.6 ± 37.6 ng/mL vs. 15.0 ± 7.04 ng/mL; p = 0.005).
Conclusions:
Higher expression of Gal-3 is an indicator of myocardial fibrosis and remodeling in decompensated HF. Therefore, galectin-3 seems to be an interesting and valuable marker of AHF.
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