Cellular Senescence in the Ascending Aorta and Complexity of Coronary Atherosclerosis
Hanife Abanus1, Mutlu Vural1, Fahrettin Katkat2
1Cardiology Department, Medical Sciences University Bağcılar Training and Research Hospital, Istanbul, Turkey.
Insights
Cellular senescence markers p16 and p21 in the aorta correlate with coronary artery disease (CAD) complexity. Higher p16 expression independently predicts more complex CAD in patients undergoing bypass surgery.
Area of Science:
- Cardiovascular Research
- Aging Biology
- Pathogenesis of Atherosclerosis
Background:
- Cellular senescence is implicated in vascular aging and atherosclerosis.
- Direct human evidence linking vascular senescence to coronary artery disease (CAD) is limited.
Purpose of the Study:
- To investigate the association between senescent cell markers in the ascending aorta and CAD complexity.
- To evaluate p16, p21, and β-galactosidase as biomarkers for CAD complexity in patients undergoing coronary artery bypass grafting (CABG).
Main Methods:
- Ascending aortic tissue samples were analyzed from 112 patients undergoing CABG.
- Immunohistochemistry assessed p16, p21, and β-galactosidase expression.
- Coronary lesion complexity was quantified using the SYNTAX score.
Main Results:
- Higher p16 and p21 expression (percentage and grade) in the aorta correlated with moderate-to-high SYNTAX scores.
- p16 expression was an independent predictor of higher SYNTAX scores (OR: 1.016, p=0.047).
- β-galactosidase showed no significant association with CAD complexity.
Conclusions:
- Increased p16 and p21 expression in the ascending aorta is linked to greater coronary atherosclerosis complexity.
- p16 emerges as an independent predictor of complex CAD, suggesting a role in vascular aging and disease progression.
Background:
Cellular senescence might have a key role in the pathogenesis of vascular aging and atherosclerosis. However, human data directly linking cellular senescence in the vascular tissue with coronary artery disease (CAD) are limited. This study aimed to investigate the relationship between the proportion of senescent cells in the ascending aorta and the complexity of CAD in patients undergoing coronary artery bypass grafting (CABG).
Methods:
Ascending aortic tissue samples were obtained from 112 patients during elective or urgent CABG surgery. Expressions of p16, p21, and β-galactosidase (β-gal) were evaluated as cellular senescence biomarkers using immunohistochemical analysis. The complexity of coronary lesions was quantified by the Synergy between PCI with Taxus and Cardiac Surgery (SYNTAX) score. Patients were stratified into low and moderate-to-high SYNTAX score groups, and biomarker expression levels were compared between these subgroups.
Results:
The proportion of p16-positive cells in the ascending aorta was significantly higher in patients with moderate-to-high SYNTAX scores, by both percentage (p = 0.015) and staining grade (p = 0.035). Similarly, p21 expression was elevated in the moderate-to-high SYNTAX group (percentage, p = 0.015; grade, p = 0.030). β-gal expression showed no significant association with CAD complexity. In multivariate logistic regression analysis, p16 expression remained an independent predictor of higher SYNTAX score (OR: 1.016; 95% CI: 1.000-1.031; p = 0.047).
Conclusion:
Increased expression of p16 and p21 in ascending aortic tissue is significantly associated with higher coronary atherosclerosis complexity in patients undergoing CABG. Among these biomarkers, p16 serves as an independent predictor of complex CAD, highlighting its potential role in vascular aging and atherosclerosis progression.
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