High-sensitivity C-reactive protein and plaque composition in patients with stable angina pectoris: a virtual
Takashi Kubo1, Yoshiki Matsuo, Yasushi Hayashi
1Department of Cardiovascular Medicine, Wakayama Medical University, Wakayama, Japan.
Insights
Elevated high-sensitivity C-reactive protein (hs-CRP) indicates more necrotic core in coronary plaques of stable angina patients. This suggests hs-CRP reflects ongoing plaque inflammation even in stable disease.
Area of Science:
- Cardiology
- Biomarkers
- Vascular Biology
Background:
- Elevated high-sensitivity C-reactive protein (hs-CRP) is linked to adverse outcomes in coronary artery disease.
- Understanding the relationship between hs-CRP and coronary plaque characteristics is crucial for managing stable angina.
Purpose of the Study:
- To investigate the association between serum hs-CRP levels and coronary plaque composition in patients with stable angina pectoris.
- To determine if hs-CRP can serve as a marker for specific plaque morphologies.
Main Methods:
- Virtual histology intravascular ultrasound (VH-IVUS) was used to analyze plaque composition.
- 113 patients with stable angina and a culprit lesion were divided into elevated (>3 mg/l) and normal hs-CRP groups.
- Correlations between hs-CRP levels and plaque components (necrotic core, calcium, fibrous tissue) were assessed.
Main Results:
- Patients with elevated hs-CRP had significantly longer culprit lesions.
- A greater percentage of necrotic core was observed in the elevated hs-CRP group compared to the normal hs-CRP group (20% vs. 16%, P=0.014).
- Serum hs-CRP levels showed a positive correlation with the percentage of necrotic core (r=0.20, P=0.037).
Conclusions:
- Elevated hs-CRP is associated with a higher proportion of necrotic core within culprit lesions in stable angina patients.
- These findings suggest that hs-CRP may indicate inflammatory activity within coronary atherosclerotic plaques, even in stable disease states.
- hs-CRP could be a valuable biomarker for assessing plaque vulnerability in stable coronary artery disease.
Objective:
Elevated high-sensitivity C-reactive protein (hs-CRP) is related to clinical outcome in coronary artery disease. We used virtual histology intravascular ultrasound to evaluate the relationship between serum hs-CRP level and coronary plaque composition in patients with stable angina pectoris.
Methods And Results:
Overall 113 consecutive patients with stable angina pectoris who had a de-novo culprit lesion were examined in this study. Patients were divided into an elevated hs-CRP group (>3 mg/l; n=40) or a normal hs-CRP group (n=73). Grayscale and virtual histology intravascular ultrasound analysis was performed across the entire culprit lesion. Mean plaque area was similar in both groups. Lesion length (18+/-5 vs. 16+/-6 mm, P<0.046) was significantly greater in the elevated hs-CRP group than that in the normal hs-CRP group. Although the percentage of dense calcium, fibrofatty tissue, and fibrous tissue was not different between the two groups, the percentage of necrotic core was significantly greater in the elevated hs-CRP group compared with the normal hs-CRP group (20+/-9 vs. 16+/-8%, P=0.014). The percentage of necrotic core was positively correlated with the serum hs-CRP level (r=0.20, P=0.037). A multivariate logistic regression model showed that the percentage of necrotic core was associated with elevated hs-CRP (P=0.019; odds ratio=1.1; 95% confidence interval=1.01-1.12).
Conclusion:
Elevated hs-CRP was related to the amount of necrotic core in the culprit lesion of stable angina pectoris. Our results suggest that elevated hs-CRP might reflect the inflammatory activity of the coronary atherosclerotic plaque even in the setting of stable angina pectoris.
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