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Updated: May 23, 2025

Coronary Progenitor Cells and Soluble Biomarkers in Cardiovascular Prognosis after Coronary Angioplasty
Published on: January 28, 2020
A-kinase anchoring protein 1: an independent predictor of coronary artery disease
Wei Yan1, Yun-Lang Dai2, Jun-Xia Han3
1Department of Geriatric Medicine, the First Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.
Insights
Lower serum levels of A-kinase anchoring protein 1 (AKAP1) are linked to coronary artery disease (CAD). This finding suggests AKAP1 may serve as a potential biomarker for predicting CAD risk in patients.
Area of Science:
- Cardiovascular Research
- Biomarker Discovery
- Molecular Cardiology
Background:
- Coronary artery disease (CAD) remains a leading global cause of mortality.
- A-kinase anchoring protein 1 (AKAP1) is expressed in the heart and is believed to play a protective role.
- Limited data exists on serum AKAP1 concentrations in CAD patients.
Purpose of the Study:
- Quantify serum AKAP1 levels in patients with CAD.
- Evaluate the predictive capability of serum AKAP1 for CAD.
- Investigate the association between AKAP1 and CAD risk.
Main Methods:
- Included 255 patients undergoing coronary angiography, categorized into CAD and non-CAD groups.
- Performed comparative analysis of clinical data and serum AKAP1 levels.
- Utilized multivariate logistic regression and ROC curve analysis to assess AKAP1's association with CAD.
Main Results:
- Serum AKAP1 concentrations were significantly lower in the CAD group compared to the non-CAD group (P < 0.01).
- Lower AKAP1 levels were independently associated with an increased risk of CAD (OR = 5.677, P = 0.005).
- ROC analysis indicated a limited but present ability of AKAP1 to predict CAD (AUC = 0.649).
Conclusions:
- Serum AKAP1 levels are inversely associated with CAD.
- AKAP1 may serve as a potential predictive marker for coronary artery disease.
- Further research is warranted to validate and elucidate these findings.
Introduction:
Coronary artery disease (CAD) is the leading cause of death worldwide. A-kinase anchoring protein 1 (AKAP1), thought to regulate the function and structure of mitochondria, is enriched in the heart, where it plays a protective role. However, data on the serum AKAP1 concentration levels in patients with CAD are currently lacking. To address this, the serum levels of AKAP1 in patients with CAD were quantified and their predictive ability for CAD was evaluated in this study.
Methods:
A total of 255 patients referred for coronary angiography were included in this study and classified into two groups (CAD and non-CAD group). A comparative analysis of clinical data and serum AKAP1 concentration levels was performed between the two groups. The patients were then divided into quartiles according to AKAP1 levels. A multivariate logistic regression model was used to assess the independent association of AKAP1 with CAD.
Results:
The CAD group showed a lower AKAP1 concentration than the non-CAD group (P < 0.01). The AKAP1 level was correlated with a history of CAD (P < 0.001). The receiver operator characteristic (ROC) curve analysis showed a low ability of AKAP1 in predicting CAD (area under the ROC curve = 0.649). Finally, in the multivariate logistic regression model with the highest quartile as the reference, the lowest quartile of AKAP1 remained significantly associated with an increased risk for CAD (odds ratio (OR) = 5.677, 95% confidence interval [CI] 1.704 to 18.912, P = 0.005).
Conclusions:
Our results confirmed that serum AKAP1 levels are inversely associated with CAD and may therefore be used as a marker for CAD prediction. But additional studies are needed to confirm and further elucidate our results.
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