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Intravascular Ultrasound Image-Based Finite Element Modeling Approach for Quantifying In Vivo Mechanical Properties of Human Coronary Artery
Published on: December 6, 2024
Relationship between hs-CRP, proMMP-1, TIMP-1 and coronary plaque morphology: intravascular ultrasound study
Xing-wei Zhang1, Jun-bo Ge, Jian-min Yang
1Department of Cardiology, Hangzhou First Municipal Hospital & Hangzhou Hospital, Nanjing Medical University, Hangzhou 310006, China.
Insights
Elevated levels of hypersensitive C-reactive protein (hs-CRP), pro-matrix metalloproteinase-1 (proMMP-1), and tissue inhibitors of matrix metalloproteinase-1 (TIMP-1) correlate with unstable coronary plaque characteristics. These blood markers can help predict plaque instability and rupture in patients with coronary heart disease.
Area of Science:
- Cardiovascular Medicine
- Biomarkers
- Interventional Cardiology
Background:
- Acute coronary syndrome (ACS) pathogenesis involves unstable plaque rupture and thrombus formation.
- Identifying blood markers for coronary plaque characteristics is significant but understudied.
- This study investigates hs-CRP, proMMP-1, and TIMP-1 in relation to coronary plaque morphology.
Purpose of the Study:
- To explore the relationship between hs-CRP, proMMP-1, TIMP-1, and coronary plaque morphology.
- To determine if these biomarkers can predict plaque instability and rupture.
- To correlate blood indexes with specific plaque characteristics identified by IVUS.
Main Methods:
- 152 patients with coronary heart disease underwent intravascular ultrasound (IVUS) before percutaneous coronary intervention.
- Plasma levels of hs-CRP, proMMP-1, and TIMP-1 were measured using ELISA.
- Coronary plaque morphology was assessed using IVUS, analyzing features like plaque area, lipid pool, and lumen size.
Main Results:
- Unstable and ruptured plaques were more prevalent in patients with acute myocardial infarction and unstable angina.
- Higher levels of hs-CRP, proMMP-1, and TIMP-1 were observed in the ruptured plaque group.
- Specific thresholds for hs-CRP, proMMP-1, and TIMP-1 demonstrated predictive value for ruptured plaques, with significant ROC curve areas.
Conclusions:
- Coronary plaque characteristics correlate with clinical presentation in ACS.
- Elevated hs-CRP, proMMP-1, and TIMP-1 levels are associated with plaque instability and rupture.
- These biomarkers show potential for predicting high-risk coronary plaques.
Background:
Rupture of unstable plaque with subsequent thrombus formation is the common pathophysiological substrate of the acute coronary syndrome (ACS). It is of potential significance to explore the blood indexes predicting plaque characteristics. Little studies have focused on this field. Therefore we investigated the relationship between hypersensitive C-reactive protein (hs-CRP), pro-matrix metalloproteinase-1 (proMMP-1), tissue inhibitors of matrix metalloproteinase-1 (TIMP-1) and coronary plaque morphology.
Methods:
Intravascular ultrasound (IVUS) examination was done in 152 patients with confirmed coronary heart disease before percutaneous coronary intervention from February 2003 to July 2005. Plasma samples of arterial blood were collected prior to the procedure. The level of hs-CRP, proMMP-1 and TIMP-1 were respectively measured by enzyme-linked immunosorbent assay (ELISA).
Results:
Unstable and ruptured plaque were found more frequently in patients with acute myocardial infarction and unstable angina. External elastic membrane cross-sectional area (EEM CSA), plaque area, lipid pool area and plaque burden were significantly larger in ruptured and unstable plaque group. Positive remolding, thinner fabric-cap, smaller minimal lumen cross-sectional area (MLA), dissection and thrombus were significantly more frequent in ruptured and unstable plaque group. The levels of plasma hs-CRP, proMMP-1 and TIMP-1 were higher in ruptured plaque group. hs-CRP > 8.94 mg/L was used to predict ruptured plaque with a ROC curve area of 0.76 [95% confidence interval (CI), 67.0% - 85.8%], sensitivity of 71.8%, specificity of 77.0% and accuracy of 69.2% (P < 0.01), similarly for proMMP-1 > 0.12 ng/ml with a ROC curve area of 0.69 [95% CI, 58.2% - 80.2%], sensitivity of 69.2%, specificity of 75.2% and accuracy of 66.2% (P < 0.01), and TIMP-1 > 83.45 ng/ml with a ROC curve area of 0.67 [95% CI, 56.2% - 78.3%], sensitivity of 66.7%, specificity of 61.9% and accuracy of 66.2% (P < 0.01).
Conclusion:
The plaque characteristics correlate with the clinical presentation. The elevation of hs-CRP, proMMP-1 and TIMP-1 are related to the plaque instability and rupture.
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