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Published on: January 28, 2020
Association of serum coiled-coil domain containing protein 11 levels with coronary artery disease
Jie Gao1, Hongping Wang1, Wenjun Wang1
1Department of Endocrinology, Putuo Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Insights
Elevated levels of coiled coil domain containing protein 11 (CCDC11) are associated with coronary artery disease (CAD). Higher CCDC11 indicates increased CAD presence and severity, suggesting its potential as a novel CAD biomarker.
Area of Science:
- Cardiovascular Research
- Biomarker Discovery
- Molecular Cardiology
Background:
- Coronary artery disease (CAD) remains a leading cause of mortality worldwide.
- Identifying novel biomarkers for early detection and risk stratification of CAD is crucial.
- The role of coiled coil domain containing protein 11 (CCDC11) in cardiovascular pathology is not well-established.
Purpose of the Study:
- To investigate the association between serum CCDC11 levels and the presence and severity of CAD.
- To evaluate CCDC11 as a potential diagnostic biomarker for CAD.
Main Methods:
- A case-control study involving 266 CAD patients and 95 controls.
- Serum CCDC11 concentrations were measured using ELISA.
- Spearman correlation, logistic regression, and ROC curve analysis were employed.
Main Results:
- Median serum CCDC11 levels were significantly higher in CAD patients compared to controls (20.4 vs. 13.8 ng/mL, P < 0.001).
- CCDC11 levels positively correlated with the number of affected coronary vessels.
- CCDC11 independently predicted CAD and showed a moderate discriminative ability (AUC = 0.71), outperforming CRP.
Conclusions:
- Elevated serum CCDC11 is significantly associated with the presence and severity of CAD.
- CCDC11 demonstrates potential as a novel and clinically valuable biomarker for CAD diagnosis and risk assessment.
Objective:
This study aimed to assess the association between circulating levels of coiled coil domain containing protein 11 (CCDC11) and coronary artery disease (CAD).
Methods:
A total of 266 patients diagnosed with CAD and 95 controls were enrolled in our center from January 2024 to December 2024. The CAD cohort was further stratified into three subgroups based on the number of affected coronary vessels: the single-vessel group (n = 88), the double-vessel group (n = 74) and the triple-vessel group (n = 104). Serum concentrations of CCDC11 were quantified using an ELISA kit. Spearman correlation analysis was employed to evaluate the relationships between CCDC11 levels and other clinical parameters. Binary logistic regression analysis was conducted to determine the independent association of CCDC11 with CAD. The discriminative ability of CCDC11 for CAD was assessed using receiver operating characteristic (ROC) curve analysis.
Results:
Median serum CCDC11 amounts were significantly elevated in the CAD group compared to controls (20.4 vs. 13.8 ng/mL, P < 0.001). Furthermore, serum CCDC11 levels demonstrated a positive trend correlating with the number of lesioned coronary vessels (P for trend < 0.001). Logistic regression analysis revealed that CCDC11 was independently correlated with CAD. In ROC analysis, the area under the ROC curve (AUC) for CCDC11 in discriminating CAD was moderate but significantly higher than that for CRP (0.71 vs. 0.56, P < 0.01). Utilizing the maximum Youden index, an optimal CCDC11 cutoff value of 19.37 ng/mL was identified, yielding a sensitivity of 53.4% and specificity of 91.6% for CAD discrimination.
Conclusions:
Elevated serum levels of CCDC11 were positively associated with both the presence and severity of CAD, suggesting that CCDC11 may serve as a novel and clinically valuable biomarker for CAD.
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