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Published on: August 28, 2018
Association between galectin-3 levels and isolated coronary artery ectasia
Gonul Aciksari1, Turgut Uygun2, Adem Atici3
1Department of Cardiology, Goztepe Training and Research Hospital, Istanbul Medeniyet University, Istanbul, Turkey.
Insights
Serum Galectin-3 (Gal-3) levels are significantly higher in patients with coronary artery ectasia (CAE), suggesting Gal-3 may play a role in CAE development. This finding could lead to new diagnostic approaches for this condition.
Area of Science:
- Cardiology
- Biomarkers
- Pathophysiology
Background:
- Coronary artery ectasia (CAE) is characterized by abnormal coronary artery dilation, with unclear underlying mechanisms.
- Histopathological similarities exist between CAE and coronary atherosclerosis.
- Galectin-3 (Gal-3) is a known biomarker for atherosclerotic lesion progression and destabilization.
Purpose of the Study:
- To investigate the relationship between serum Galectin-3 (Gal-3) levels and isolated coronary artery ectasia (CAE).
- To explore Gal-3 as a potential biomarker in the context of isolated CAE.
Main Methods:
- A prospective, case-controlled study involving 49 isolated CAE patients and 43 controls.
- Coronary angiography was used for CAE diagnosis.
- Serum Gal-3 concentrations were measured, alongside physical examination, medical history, blood biochemistry, and echocardiography.
Main Results:
- Median Gal-3 levels were significantly higher in isolated CAE patients compared to controls (p < 0.001).
- No correlation was found between the extent of CAE and Gal-3 levels (p = 0.41).
- Multivariate regression analysis identified Gal-3 concentration as an independent predictor of isolated CAE.
Conclusions:
- Elevated serum Gal-3 concentrations in patients with isolated CAE suggest its involvement in the pathogenesis of the condition.
- Gal-3 may serve as a significant biomarker for isolated CAE.
Background:
Coronary artery ectasia (CAE) is a well-recognised disorder characterised by abnormal dilation of the coronary arteries. Underlying mechanisms associated with abnormal luminal dilation in CAE remain to be elucidated. However, histopathological features resemble those of coronary atherosclerosis. Galectin-3 (Gal-3) is a valuable biomarker for both progression and destabilisation of atherosclerotic lesions. To the best of our knowledge, there is no study in the literature examining serum Gal-3 levels in patients with isolated CAE. In the present study, therefore, we aimed to investigate the possible relationship between serum Gal-3 levels and isolated CAE.
Methods:
Between March 2016 and March 2017 this prospective, case-controlled study included a total of 49 consecutive isolated CAE patients (31 males, 18 females) diagnosed with CAE by coronary angiography at the catheter laboratory of Medeniyet University, Goztepe Training and Research Hospital, and 43 individuals (19 males, 24 females) with normal coronary arteries. Physical examination, medical history, blood biochemistry and transthoracic echocardiography were performed in both groups. Serum concentrations of Gal-3 were measured using blood samples.
Results:
Median Gal-3 levels were significantly higher in isolated CAE patients than in the controls [23.2 (23.9 ± 7.1) vs 16.8 ng/ml (17.8 ± 7.3); p < 0.001]. According to the Markis classification, the extent of CAE was not correlated with Gal-3 levels (p = 0.41). Multivariate regression analysis revealed that Gal-3 concentration was an independent predictor of isolated CAE.
Conclusions:
Our study results suggest that Gal-3 serum concentrations significantly increased in patients with isolated CAE, indicating that Gal-3 may be involved in the pathogenesis of isolated CAE.
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