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Published on: January 28, 2020
Galectin-3 and Coronary Artery Disease: An Inflammation-Based Approach
Rıdvan Bora1, Rojda Tanrıverdi2, Şenay Balcı Fidancı2
1Department of Cardiology, Mersin City Education and Research Hospital, 33800 Mersin, Turkey.
Insights
Elevated Galectin-3 levels indicate inflammation in coronary artery disease but do not reliably distinguish between acute and chronic coronary syndrome. Further research is needed to clarify its clinical value as a biomarker.
Area of Science:
- Cardiovascular Medicine
- Biomarkers
- Inflammation and Immunology
Background:
- Coronary artery disease (CAD) is a chronic inflammatory condition involving atherosclerosis with varied clinical presentations.
- Galectin-3, a protein involved in inflammation and fibrosis, is explored as a potential cardiovascular biomarker.
- The diagnostic utility of Galectin-3 across different CAD stages is not well-established.
Purpose of the Study:
- To investigate the diagnostic significance of serum Galectin-3 concentrations in patients with different clinical stages of coronary artery disease.
- To evaluate Galectin-3 as a potential biomarker for distinguishing between acute coronary syndrome and chronic coronary syndrome.
Main Methods:
- Prospective study of 180 participants undergoing coronary angiography, categorized into control, acute coronary syndrome, and chronic coronary syndrome groups.
- Serum Galectin-3 levels measured via enzyme-linked immunosorbent assay.
- Statistical analyses included non-parametric tests, correlation, receiver operating characteristic (ROC) curve analysis, and multivariable logistic regression.
Main Results:
- Galectin-3 concentrations were significantly higher in both acute and chronic coronary syndrome groups compared to controls (p < 0.001).
- No significant difference in Galectin-3 levels was found between acute and chronic coronary syndrome groups.
- ROC analysis revealed limited diagnostic performance for Galectin-3 in identifying acute coronary syndrome (AUC 0.617) and poor performance for chronic coronary syndrome (AUC 0.541).
- Galectin-3 was not an independent predictor; age and smoking predicted acute coronary syndrome, while age and male sex predicted chronic coronary syndrome.
Conclusions:
- Elevated Galectin-3 levels in CAD patients reflect the inflammatory burden of atherosclerosis.
- Galectin-3 shows limited ability to discriminate between acute and chronic coronary syndrome.
- Larger prospective studies are necessary to determine the definitive clinical value of Galectin-3 in CAD management.
Abstract:
Background/Objectives: Coronary artery disease is a chronic inflammatory disorder characterized by progressive atherosclerosis and heterogeneous clinical presentations ranging from acute coronary events to stable ischemic conditions. Galectin-3 is a β-galactoside-binding lectin involved in inflammatory responses, fibrosis, and tissue remodeling, and has been investigated as a potential biomarker in cardiovascular diseases. However, its diagnostic significance across different clinical stages of coronary artery disease remains unclear. Methods: This prospective study included 180 participants who underwent coronary angiography and were classified into three groups: control (n = 60), acute coronary syndrome (n = 60), and chronic coronary syndrome (n = 60). Serum Galectin-3 concentrations were measured using an enzyme-linked immunosorbent assay. Group comparisons were performed using non-parametric statistical tests. Correlation analysis, receiver operating characteristic curve analysis, and multivariable logistic regression were conducted to evaluate diagnostic performance and independent associations. Results: Galectin-3 concentrations were significantly higher in both acute coronary syndrome and chronic coronary syndrome groups compared with the control group (p < 0.001), whereas no significant difference was observed between the two disease groups. Receiver operating characteristic analysis demonstrated limited diagnostic performance for identifying acute coronary syndrome (area under the curve 0.617, sensitivity 96.7%, specificity 43.3%, p = 0.027) and poor diagnostic performance for chronic coronary syndrome (area under the curve 0.541, sensitivity 91.7%, specificity 30.0%, p = 0.436). In multivariable analysis, Galectin-3 was not identified as an independent predictor of either clinical condition. Age and smoking were independently associated with acute coronary syndrome, while age and male sex were independently associated with chronic coronary syndrome. Conclusions: Galectin-3 levels are elevated in patients with coronary artery disease and appear to reflect the inflammatory burden associated with atherosclerosis. However, its diagnostic discrimination between different clinical stages of coronary artery disease remains limited. Larger prospective studies are required to clarify its clinical value.
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