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Coronary Progenitor Cells and Soluble Biomarkers in Cardiovascular Prognosis after Coronary Angioplasty
Published on: January 28, 2020
Decreased serum SIRT6 as a novel predictor of coronary artery disease
1Department of Cardiology, The Second Hospital, Cheeloo College of Medicine, Shandong University, Jinan, Shandong, China. luqinghua126@yeah.net.
Insights
Serum SIRT6 levels are significantly lower in patients with coronary artery disease (CAD), including stable angina and acute coronary syndrome. This decrease is independently associated with CAD diagnosis, suggesting SIRT6 may have a cardioprotective role.
Area of Science:
- Biochemistry
- Cardiovascular Research
- Molecular Biology
Background:
- SIRT6 is a histone deacetylase involved in aging, inflammation, and metabolism.
- Its role in atherosclerosis suggests potential involvement in coronary artery disease (CAD).
Purpose of the Study:
- To investigate the association between serum SIRT6 levels and CAD.
- To determine if SIRT6 expression differs between CAD patients and healthy controls.
Main Methods:
- Serum samples from 69 CAD patients (30 stable angina, 39 acute coronary syndrome) and 16 controls were analyzed.
- SIRT6 expression was measured using Western blotting and ELISA.
- Correlations with CAD markers and logistic regression were performed.
Main Results:
- Serum SIRT6 levels were significantly lower in both stable angina and acute coronary syndrome patients compared to controls.
- Lower SIRT6 levels correlated positively with HDL cholesterol and age, and negatively with blood glucose.
- Reduced SIRT6 was independently associated with CAD in men and could distinguish CAD patients from controls.
Conclusions:
- Decreased serum SIRT6 concentration is linked to CAD.
- SIRT6 may possess a cardioprotective function in CAD.
- Further research is needed to elucidate SIRT6's role in CAD.
Objective:
SIRT6 is an NAD-dependent histone deacetylase known to regulate aging, inflammation and energy metabolism, and might play an important role in atherosclerosis. However, whether it also plays a role in coronary artery disease (CAD) remains unclear.
Patients And Methods:
In this study, we detected the expression of SIRT6 in serum by Western blotting. The concentrations of SIRT6 in serum specimens from 69 patients with CAD [30 with stable angina (SA) and 39 with acute coronary syndrome (ACS)] and 16 controls were analysed using the enzyme-linked immunosorbent assay (ELISA) method.
Results:
Western blotting analysis of the serum samples found that SIRT6 expression was decreased in the SA group (p=0.000) and ACS group (p=0.000) compared with the control group. Significantly lower levels of serum SIRT6 were observed in SA patients (18.80±9.14 ng/mL) and ACS patients (16.85±9.66 ng/mL) than in healthy controls (25.79±14.23 ng/mL). SIRT6 concentrations were positively correlated with other markers of CAD, such as high-density lipoprotein cholesterol (r=0.362, p<0.01) and age (r=0.265, p<0.05), and negatively correlated with blood glucose (r=-0.284, p<0.05). Multivariate logistic regression analysis demonstrated that lower SIRT6 levels were independently associated with the presence of CAD in men (OR=0.817, 95% CI 0.694-0.962, p=0.015). Receiver operating characteristic (ROC) curve analysis showed that lower serum SIRT6 could distinguish CAD patients (AUC, 0.726; 95% CI, 0.508-0.943; p=0.041) from controls. SIRT6 is found downregulated in blood vessels of atherosclerotic APOE-/- mice and human aorta arteries.
Conclusions:
We demonstrated that SA and ACS patients had lower serum concentrations of SIRT6. The decreased serum SIRT6 level was independently associated with the diagnosis of CAD. SIRT6 may play a cardioprotective role in CAD patients, and future research is required to address this issue.
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