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Published on: January 28, 2020
Intermediate CD14++CD16+ monocyte predicts severe coronary stenosis and extensive plaque involvement in asymptomatic
Shyh-Chyi Lo1, Wen-Jeng Lee2,3,4, Ching-Yi Chen5
1Department of Laboratory Medicine, National Taiwan University Hospital and National Taiwan University College of Medicine, Taipei, Taiwan.
Insights
High counts of intermediate CD14++CD16+ monocytes predict severe coronary artery disease (CAD) and extensive plaque in asymptomatic adults. This finding aids in improving cardiovascular risk stratification beyond traditional scores.
Area of Science:
- Cardiovascular Medicine
- Immunology
- Medical Diagnostics
Background:
- Circulating leukocyte subtypes and monocyte subsets are established predictors of cardiovascular events.
- Previous research suggests a link between specific leukocyte populations and cardiovascular pathology.
Purpose of the Study:
- To investigate the association between leukocyte subtypes, particularly monocyte subsets, and the severity of coronary artery stenosis and plaque burden in asymptomatic adults.
- To determine if intermediate CD14++CD16+ monocyte counts can independently predict severe coronary artery disease (CAD) and improve cardiovascular risk stratification.
Main Methods:
- Retrospective analysis of clinical, laboratory, and coronary CT data from 588 asymptomatic adults.
- Assessment of leukocyte and monocyte subset counts, including classical (CD14++CD16-) and intermediate (CD14++CD16+) monocytes.
- Correlation of monocyte subset counts with mixed, calcified, and non-calcified plaque scores, and prediction of severe coronary stenosis and extensive plaque involvement, adjusted for Framingham Risk Score (FRS), metabolic syndrome, and C-reactive protein.
Main Results:
- Intermediate CD14++CD16+ monocyte count showed the strongest association with mixed and calcified plaque scores.
- Neutrophils and classical CD14++CD16- monocytes were associated with non-calcified plaque score.
- High intermediate CD14++CD16+ monocyte count (>12 cells/μL) independently predicted extensive plaque involvement (OR 3.16) and severe coronary stenosis (OR 3.67).
- Adding intermediate CD14++CD16+ monocyte count to FRS significantly improved risk reclassification for extensive plaque and severe stenosis, especially in the intermediate-risk group.
Conclusions:
- Intermediate CD14++CD16+ monocyte count is an independent predictor of severe coronary artery disease and extensive plaque involvement in asymptomatic individuals.
- This monocyte subset can enhance cardiovascular risk stratification when combined with traditional risk factors like the Framingham Risk Score.
- The findings suggest a potential role for monitoring intermediate CD14++CD16+ monocytes in early detection and management of cardiovascular disease.
Abstract:
Circulating leukocyte subtypes and monocyte subsets are independent predictors of cardiovascular events. We hypothesized that an increased leukocyte subtype would predict severe coronary stenosis and extensive plaque involvement. We retrospectively analyzed clinical, laboratory, and coronary CT data in a total of 588 asymptomatic adults (69% men; mean age, 57 ± 9 years) undergoing a general health check-up. Intermediate CD14++CD16+ monocyte count had the strongest association with mixed and calcified plaque scores, whereas the numbers of neutrophils and classical CD14++CD16- monocytes were significantly associated with non-calcified plaque score. Only high CD14++CD16+ monocyte count (>12 cells/μL) significantly predicted extensive plaque involvement [odds ratio 3.16 (95% confidence interval 1.84-5.43), P < 0.001; quartile 4 vs. 1-3] and severe coronary stenosis [3.67 (1.84-7.33), P < 0.001; quartile 4 vs. 1-3] after adjustments for Framingham Risk Score (FRS), metabolic syndrome, and C-reactive protein. The CD14++CD16+ monocyte count, when added to FRS, significantly reclassified 30.4 and 26.7% of the overall and 50.2 and 36.2% of the intermediate-risk population (FRS 6-20%) for predicting extensive plaque involvement and severe coronary stenosis, respectively. Thus, in asymptomatic individuals, intermediate CD14++CD16+ monocyte could independently predict severe CAD and improve risk stratification.
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