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Published on: October 12, 2017
Complex association of apolipoprotein E-containing HDL with coronary artery disease burden in cardiovascular disease
Alexander V Sorokin1, Nidhi Patel2, Khaled M Abdelrahman2
1Section of Lipoprotein Metabolism, Translational Vascular Medicine Branch, and.
Insights
Low apolipoprotein E-containing HDL-cholesterol (ApoE-HDL-C) is linked to more severe coronary artery disease (CAD). High apolipoprotein C-III (ApoC-III) in HDL may be a stronger predictor of CAD severity.
Area of Science:
- Cardiovascular Medicine
- Biomarker Discovery
- Lipid Metabolism
Background:
- Traditional cardiovascular disease (CVD) risk prediction methods need improvement.
- Emerging biomarkers may offer enhanced diagnostic capabilities for CVD.
- Apolipoprotein E-containing HDL-cholesterol (ApoE-HDL-C) is an emerging biomarker.
Purpose of the Study:
- To investigate the association between ApoE-HDL-C and coronary plaque characteristics.
- To explore the role of apolipoprotein C-III (ApoC-III) in HDL in CVD risk.
- To evaluate novel biomarkers for improved CVD risk prediction.
Main Methods:
- Prospective observational study of 795 individuals with extensive cardiometabolic profiling.
- Coronary artery calcium (CAC) scoring and quantitative coronary computed tomography angiography (CCTA) were performed.
- Measurements included ApoE-HDL-C, ApoC-III, and other lipid parameters.
Main Results:
- Low ApoE-HDL-C was associated with more severe coronary stenosis and higher CAC scores.
- Quantitative CCTA revealed lower noncalcified burden (NCB) in high ApoE-HDL-C groups.
- ApoC-III in HDL demonstrated a more robust predictive value for CAD than ApoE-HDL-C.
Conclusions:
- ApoE-HDL-C is significantly associated with early coronary plaque characteristics.
- ApoE-HDL-C levels are influenced by ApoC-III concentrations.
- Low ApoE-HDL-C and high ApoC-III may serve as important markers for CVD severity.
Abstract:
BackgroundAlthough traditional lipid parameters and coronary imaging techniques are valuable for cardiovascular disease (CVD) risk prediction, better diagnostic tests are still needed.MethodsIn a prospective, observational study, 795 individuals had extensive cardiometabolic profiling, including emerging biomarkers, such as apolipoprotein E-containing HDL-cholesterol (ApoE-HDL-C). Coronary artery calcium (CAC) score was assessed in the entire cohort, and quantitative coronary computed tomography angiography (CCTA) characterization of total burden, noncalcified burden (NCB), and fibrous plaque burden (FB) was performed in a subcohort (n = 300) of patients stratified by concentration of ApoE-HDL-C. Total and HDL-containing apolipoprotein C-III (ApoC-III) were also measured.ResultsMost patients had a clinical diagnosis of coronary artery disease (CAD) (n = 80.4% of 795), with mean age of 59 years, a majority being male (57%), and about half on statin treatment. The low ApoE-HDL-C group had more severe stenosis (11% vs. 2%, overall P < 0.001), with higher CAC as compared with high ApoE-HDL-C. On quantitative CCTA, the high ApoE-HDL-C group had lower NCB (β = -0.24, P = 0.0001), which tended to be significant in a fully adjusted model (β = -0.32, P = 0.001) and altered by ApoC-III in HDL levels. Low ApoE-HDL-C was significantly associated with LDL particle number (β = 0.31; P = 0.0001). Finally, when stratified by FB, ApoC-III in HDL showed a more robust predictive value of CAD over ApoE-HDL-C (AUC: 0.705, P = 0.0001) in a fully adjusted model.ConclusionApoE-containing HDL-C showed a significant association with early coronary plaque characteristics and is affected by the presence of ApoC-III, indicating that low ApoE-HDL-C and high ApoC-III may be important markers of CVD severity.Trial RegistrationClinicalTrials.gov: NCT01621594.FundingThis work was supported by the NHLBI at the NIH Intramural Research Program.
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