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Published on: May 6, 2014
Relationship between serum vasoactive factors and plaque morphology in patients with non-ST-segment elevated acute
Ya-feng Lu1, Shu-zheng Lü, Yun-dai Chen
1Department of Cardiology, Beijing Anzhen Hospital, Capital Medical University, Beijing Institute of Heart Lung and Blood Vessel Disease, Beijing 100029, China.
Insights
Interleukin-18 (IL-18) and placental growth factor (PLGF) are key biomarkers for identifying vulnerable plaques in patients with non-ST-segment elevated acute coronary syndrome (ACS). These factors can help predict plaque vulnerability and aid in diagnosis.
Area of Science:
- Cardiovascular Medicine
- Biomarkers
- Vascular Biology
Background:
- Vasoactive factors are linked to vulnerable plaque and acute coronary syndrome (ACS).
- Understanding these factors is crucial for managing non-ST-segment elevated ACS.
- Plaque morphology assessment is vital in ACS patient stratification.
Purpose of the Study:
- To investigate the relationship between specific vasoactive factors and plaque morphology.
- To determine the predictive value of serum vasoactive factors in non-ST-segment elevated ACS.
- To assess biomarkers for vulnerable plaque identification.
Main Methods:
- 124 patients with non-ST-segment elevated ACS underwent coronary angiography and intravascular ultrasound.
- Serum levels of soluble vascular endothelial growth factor receptor-1 (sFlt-1), placental growth factor (PLGF), and interleukin-18 (IL-18) were measured.
- Vasoactive factor levels were compared between vulnerable and stable plaque groups, and between unstable angina pectoris (UAP) and non-ST-segment elevation acute myocardial infarction (NSTE-AMI) groups.
Main Results:
- sFlt-1 and PLGF levels were significantly higher in the vulnerable plaque group compared to the stable plaque group.
- IL-18 levels showed a positive correlation with plaque morphology.
- PLGF was identified as an independent risk factor for vulnerable plaque (OR=2.115, P=0.018) and a significant diagnostic factor (AUC=0.799, sensitivity 86%, specificity 63%).
Conclusions:
- Both IL-18 and PLGF serve as valuable biomarkers for vulnerable plaques.
- These factors are helpful in predicting vulnerable plaque development in ACS patients.
- PLGF demonstrates significant diagnostic utility for vulnerable plaque identification.
Background:
Vasoactive factors have been reported to correlate with vulnerable plaque and acute coronary syndrome (ACS). This study aimed to investigate the relationship between vasoactive factors and plaque morphology in patients suffering from non-ST-segment elevated ACS.
Methods:
From April 2007 to April 2009, 124 consecutive patients suffering from non-ST-segment elevated ACS who had received coronary angiography (CAG) and intravascular ultrasound (IVUS) in the People's Liberation Army General Hospital and Beijing Anzhen Hospital were enrolled in this study. Three serum vasoactive factors, plasma soluble vascular endothelial growth factor receptor-1 (sFlt-1), placental growth factor (PLGF) and interleukin-18 (IL-18), were measured by enzyme-linked-immunosorbent serologic assay of the patients. The levels of vasoactive factors were compared between vulnerable plaque group and stable plaque group, and between unstable angina pectoris (UAP) group and non-ST-segment elevation acute myocardial infarction (NSTE-AMI) group. The relationship between the plaque morphology and levels of vasoactive factors was analyzed.
Results:
The levels of vasoactive factors were similar between the UAP group (69 patients) and NSTE-AMI group (55 patients). The levels of sFlt-1 and PLGF in the vulnerable plaque group were significantly higher than those in the stable plaque group. The level of IL-18 was correlated positively with plaque morphology. Multivariate Logistic regression analysis showed that the level of PLGF was an independent risk factor for vulnerable plaque (OR=2.115, 95% CI 1.415-5.758, P=0.018). Using the ROC curve, PLGF was a significant factor for the diagnosis of vulnerable plaque (the diagnostic point was 26.3 ng/L, the proportion of square area under the ROC curve was 0.799, 95%CI 0.758-0.839, P<0.001; the sensitivity of PLGF under the ROC curve was 86%, and the specificity 63%).
Conclusion:
Both IL-18 and PLGF are biomarkers for vulnerable plaques and helpful to predict vulnerable plaque.
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