Related Experiment Video
Updated: Sep 1, 2025

An Experimental Model of Myocardial Infarction for Studying Cardiac Repair and Remodeling in Knockout Mice
Published on: July 14, 2023
The prognostic role of galectin-3 and endothelial function in patients with heart failure
Vasiliki Tsigkou1,2, Gerasimos Siasos1,2,3, Evangelos Oikonomou4,5
1Department of Cardiology, 'Hippokration' General Hospital, National and Kapodistrian University of Athens, School of Medicine, Athens, Greece.
Insights
Flow-mediated dilatation improved with left ventricular ejection fraction in ischemic heart failure patients. Worse FMD and higher galectin-3 levels are linked to major adverse cardiovascular events, aiding risk stratification.
Area of Science:
- Cardiology
- Vascular Biology
- Biomarkers
Background:
- Heart failure (HF) is classified into HFrEF, HFmrEF, and HFpEF.
- Endothelial dysfunction (FMD), arterial stiffness (PWV), and galectin-3 are linked to MACE in ischemic HF.
- Understanding these markers' relationship with HF subtypes and outcomes is crucial.
Purpose of the Study:
- To investigate the association between FMD, PWV, galectin-3, and LVEF in ischemic HF patients.
- To determine the predictive value of these markers for MACE.
- To explore their role in stratifying risk across different HF classifications.
Main Methods:
- Prospective enrollment of 340 stable ischemic HF patients.
- Assessment of brachial artery FMD, carotid-femoral PWV, and serum galectin-3 levels.
- Follow-up for MACE, analyzed by HF group and marker levels.
Main Results:
- FMD showed a stepwise improvement with increasing LVEF (HFpEF > HFmrEF > HFrEF), significant after confounder adjustment.
- PWV was not associated with LVEF.
- Worse FMD values and higher galectin-3 tertiles were significantly associated with increased MACE.
Conclusions:
- Flow-mediated dilatation demonstrates a linear improvement with LVEF in ischemic HF.
- Deteriorated FMD and elevated galectin-3 are associated with MACE, suggesting their utility in risk stratification.
- Galectin-3 may aid in identifying high-risk ischemic HF patients.
Background:
Heart failure (HF) is nowadays classified as HF with reduced ejection fraction (HFrEF), HF with mildly reduced EF (HFmrEF), and HF with preserved EF (HFpEF). Endothelial dysfunction (assessed by flow-mediated dilatation [FMD]), increased arterial stiffness (assessed by carotid-femoral pulse-wave velocity [PWV]), and galectin-3, a biomarker of myocardial fibrosis, have been linked to major adverse cardiovascular events (MACE) in patients with ischemic HF.
Methods:
In this study we prospectively enrolled 340 patients with stable ischemic HF. We assessed the brachial artery FMD, carotid-femoral PWV, and galectin-3 levels, and patients were followed up for MACE according to HF group.
Results:
Interestingly, the FMD values exhibited a stepwise improvement according to left ventricular ejection fraction (LVEF) (HFrEF: 4.74 ± 2.35% vs. HFmrEF: 4.97 ± 2.81% vs. HFpEF: 5.94 ± ± 3.46%, p = 0.01), which remained significant after the evaluation of possible confounders including age, sex, cardiovascular risk factors, and number of significantly stenosed epicardial coronary arteries (b coefficient: 0.990, 95% confidence interval: 0.166-1.814, p = 0.019). Single-vessel coronary artery disease was more frequent in the group of HFpEF (HFrEF: 56% vs. HFmrEF: 64% vs. HFpEF: 73%, p = 0.049). PWV did not display any association with LVEF. Patients who presented MACE exhibited worse FMD values (4.51 ± 2.35% vs. 5.32 ± 2.67%, p = 0.02), and the highest tertile of galectin-3 was linked to more MACEs (36% vs. 5.9%, p = 0.01).
Conclusions:
Flow-mediated dilatation displayed a linear improvement with LVEF in patients with ischemic HF. Deteriorated values are associated with MACE. Higher levels of galectin-3 might be used for risk stratification of patients with ischemic HF.
Related Concept Videos
Heart Failure III: Clinical Manifestations
Heart Failure II: Pathophysiology
Pathophysiology of Heart Failure
Heart Failure IV: Classification and Diagnostic Evaluation
Heart Failure VII: Nursing Interventions
Cardiomyopathy III: Hypertrophic Cardiomyopathy

