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Galectin-3 as a Prognostic Biomarker in Patients with First Acute Myocardial Infarction without Heart Failure
Rada M Vucic1,2, Olivera M Andrejic3, Dragana Stokanovic4
1Department of Internal Medicine, Faculty of Medical Sciences, University of Kragujevac, Svetozara Markovica Street 69, 34000 Kragujevac, Serbia.
Insights
Galectin-3 (Gal-3) plasma levels measured within 24 hours of acute myocardial infarction (AMI) onset predict major adverse cardiovascular events (MACE). Aortic root Gal-3 concentration is a strong prognostic marker for six-month MACE in AMI patients.
Area of Science:
- Cardiology
- Biomarker Discovery
- Clinical Prognostics
Background:
- Galectin-3 (Gal-3) is implicated in cardiac remodeling post-acute myocardial infarction (AMI).
- Prognostic markers are crucial for improving survival and quality of life in AMI patients.
Purpose of the Study:
- To evaluate Galectin-3 (Gal-3) plasma concentration as a prognostic biomarker in patients with acute myocardial infarction (AMI).
- To assess the predictive value of Gal-3 for major adverse cardiovascular events (MACE) within six months post-AMI.
Main Methods:
- Included 59 patients with AMI and preserved ejection fraction.
- Measured Gal-3 plasma concentration within 24 hours of chest pain onset from multiple sites (aortic root, femoral/radial artery, coronary sinus, cubital vein).
- Evaluated Major Adverse Cardiovascular Events (MACE) at six-month follow-up.
Main Results:
- Twenty patients (34%) experienced MACE at six months post-AMI.
- Aortic root and femoral/radial artery Gal-3 concentrations independently predicted six-month MACE.
- Aortic root Gal-3 concentration (cut-off ≥ 10.86 ng/mL) showed superior predictive value for MACE or death (AUC 0.858) compared to femoral/radial artery measurements.
Conclusions:
- Galectin-3 plasma concentration, particularly from the aortic root, measured during coronary angiography within 24 hours of chest pain onset, is a valuable prognostic biomarker in AMI patients.
- This finding aids in identifying patients at higher risk for adverse cardiovascular events within six months post-AMI.
Background:
Galectin-3 (Gal-3) is a biomarker involved in a wide range of diseases including cardiac remodeling following acute myocardial infarction (AMI). Identification of prognostic markers in patients with AMI can guide strategies towards improved survival and quality of life.
Methods:
Our study included 59 patients with AMI and a preserved ejection fraction. We determined the Gal-3 plasma concentration within 24 h of chest pain onset from the aortic root, femoral/radial artery, coronary sinus and cubital vein. Major adverse cardiovascular events (MACEs) were evaluated at six months follow-up.
Results:
MACE at six months post-AMI was recorded in 20 patients (34%). The Gal-3 plasma concentration from the aortic root and the femoral/radial artery were independent predictors of MACE at six months follow-up after the first AMI (OR 1.228; 95%CI: 1.011-1.491; p = 0.038; OR 3.438; 95%CI: 1.275-9.265; p = 0.015). ROC analysis identifies the Gal-3 plasma concentration from the aortic root as a better predictor of MACE or death (cut-off ≥ 10.86 ng/mL; AUC 0.858; 95%CI: 0.744-0.973; p < 0.001) than Gal-3 plasma concentration from the femoral/radial artery (cut-off ≥ 10.18 ng/mL; AUC 0.742; 95%CI: 0.596-0.888; p = 0.006).
Conclusion:
the Gal-3 plasma concentration in patients with AMI determined during coronary angiography, especially from the aortic root, within 24 h after chest pain onset is a valuable biomarker of prognosis at six months follow-up.
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