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Updated: Jul 15, 2026

Interventional Diagnostic Procedure: A Practical Guide for the Assessment of Coronary Vascular Function
Published on: March 15, 2022
Vasodilator-stimulated phosphoprotein phosphorylation analysis prior to percutaneous coronary intervention for
L Bonello1, F Paganelli, M Arpin-Bornet
1Département de Cardiologie, Hôpital Universitaire Nord, Chemin des Bourrely, Marseille, France.
Insights
Vasodilator-stimulated phosphoprotein (VASP) analysis predicts major adverse cardiovascular events (MACE) after percutaneous coronary intervention (PCI). This test effectively identifies patients at low risk for MACE, ensuring better clinical outcomes.
Area of Science:
- Cardiology
- Pharmacogenomics
- Biomarker Discovery
Background:
- High rates of major adverse cardiovascular events (MACE) persist despite dual antiplatelet therapy post-percutaneous coronary intervention (PCI).
- Interindividual variability in clopidogrel response and its link to clinical outcomes are recognized.
- Clopidogrel resistance is a significant concern in patients undergoing PCI.
Purpose of the Study:
- To assess the predictive value of platelet reactivity index (PRI), measured by vasodilator-stimulated phosphoprotein (VASP) phosphorylation analysis, for MACE.
- To determine the efficacy of VASP analysis in predicting post-PCI MACE.
- To investigate VASP phosphorylation as a biomarker for clopidogrel response and MACE risk.
Main Methods:
- Prospective monocentric study involving 144 patients undergoing PCI.
- Platelet reactivity (PR) assessed by VASP phosphorylation 24 hours after a 300-mg clopidogrel loading dose.
- MACE recorded over a 6-month follow-up period; patients stratified into PRI quintiles via VASP analysis.
Main Results:
- A total of 144 patients with various coronary syndromes were included.
- Twenty-one MACE occurred during follow-up; patients in the lowest VASP quintile had significantly lower MACE risk (P < 0.01).
- Receiver operating characteristic (ROC) curve analysis identified an optimal VASP cut-off of 50% PR for excluding MACE, with 100% negative predictive value.
Conclusions:
- VASP phosphorylation analysis is a valuable tool for assessing individual clopidogrel response before PCI.
- This method effectively predicts postprocedural MACE in patients undergoing PCI.
- VASP analysis offers a reliable method to identify patients at low risk for MACE, guiding therapeutic decisions.
Background:
Despite dual antiplatelet therapy, the rate of major adverse cardiovascular events (MACE) after percutaneous coronary angioplasty remains high. Studies have shown interindividual variations in response to clopidogrel. Furthermore, there is an apparent link between clinical outcomes and clopidogrel resistance.
Objectives:
To investigate the value of platelet reactivity index (PRI), assessed by vasodilator-stimulated phosphoprotein (VASP) phosphorylation analysis, for predicting MACE after percutaneous coronary intervention (PCI) with stent implantation.
Methods:
A prospective monocentric study was performed on 144 patients undergoing PCI. PR was evaluated by VASP phosphorylation analysis 24 h after they received a 300-mg loading dose of clopidogrel. MACE were recorded during a 6-month follow-up. Patients were divided into quintiles according to PRI, as assessed by VASP analysis. The receiver operating characteristic (ROC) curve served to determine the optimal cut-off value of VASP analysis to detect MACE.
Results:
Of the 144 patients, 34% had stable angina pectoris, 40% silent ischemia, and 26% low-risk non-ST-segment elevation acute coronary syndrome. During the follow-up, 21 MACE were observed. Patients in quintile 1 of VASP analysis had a significantly lower risk of MACE as compared with those among the four higher quintiles (0 vs. 21, P < 0.01). ROC curve analysis of VASP showed an optimal cut-off value of 50% PR to exclude MACE. The negative predictive value of the test was 100%.
Conclusions:
VASP phosphorylation analysis can evaluate the individual response to clopidogrel loading dose prior to PCI and predict postprocedural MACE.
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