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Updated: Jul 11, 2025

Interventional Diagnostic Procedure: A Practical Guide for the Assessment of Coronary Vascular Function
Published on: March 15, 2022
Technically Challenging Percutaneous Interventions of Chronic Total Occlusions Are Associated with Enhanced Platelet
Ádám Illési1,2, Zsolt Fejes3, Marianna Pócsi3
1Department of Cardiology, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary.
Insights
Chronic total occlusion percutaneous coronary intervention (CTO-PCI) can activate platelets and affect microRNA levels. While these procedures may cause temporary platelet activation and endothelial dysfunction, they are not linked to increased adverse clinical events.
Area of Science:
- Cardiovascular Medicine
- Interventional Cardiology
- Biomarkers
Background:
- Percutaneous coronary intervention (PCI) is a key treatment for chronic total occlusion (CTO).
- CTO-PCI procedures are complex and can induce stress, potentially leading to platelet activation.
- Circulating microRNAs (miRs) are implicated in platelet and endothelial function.
Purpose of the Study:
- To assess the impact of CTO-PCI on platelet activation.
- To evaluate changes in plasma levels of miR-223, miR-181b, and miR-126 post-CTO-PCI.
- To correlate procedural characteristics with these biomarkers and clinical outcomes.
Main Methods:
- Prospective study of 50 patients undergoing CTO-PCI.
- Blood samples collected pre-PCI, 2 days post-PCI, and 3-6 months post-PCI.
- Assessed platelet activation markers (P-selectin, soluble P-selectin) and plasma miR levels.
Main Results:
- Higher Japanese CTO scores and longer PCI duration correlated with elevated P-selectin levels post-procedure.
- Longer PCI duration and higher CTO scores were associated with increased soluble P-selectin at 3-6 months.
- Shorter total stent length was linked to decreased miR-181b expression at 3-6 months; miR-223 and miR-126 showed no significant changes.
- One case of stent thrombosis occurred during follow-up.
Conclusions:
- CTO-PCI can lead to immediate platelet activation and potential long-term endothelial cell dysfunction.
- Biomarker changes, particularly miR-181b, are associated with procedural complexity and stent characteristics.
- Despite biomarker alterations, CTO-PCI was not associated with an increase in adverse clinical events in this cohort.
Abstract:
Percutaneous coronary intervention (PCI) is a frequently performed treatment option for recanalization in patients with chronic total occlusion (CTO). As CTO-PCIs are often complicated and challenging for interventionalists, the stressful and damaging nature of the procedure can be remarkable, thus platelets can be easily activated. Our aim was to investigate the effect of CTO-PCI on platelet activation and the expression of selected circulating microRNAs (miR) of platelet and endothelium origin after CTO-PCI. In this study, 50 subjects after CTO-PCI were enrolled. Blood samples were obtained before PCI, at 2 days and 3-6 months after the procedure to measure the degree of platelet activation and the level of plasma miR-223, miR-181b, and miR-126. Patients were divided based on the characteristics of the intervention. Patients with higher Japanese CTO scores and longer duration of PCI showed significantly elevated platelet P-selectin positivity (p = 0.004 and p = 0.013, respectively) 2 days after the procedure compared to pre-PCI and increased concentration of soluble P-selectin 3-6 months after the intervention (higher Japanese CTO score: p = 0.028 and longer duration of PCI: p = 0.023) compared to baseline values. Shorter total stent length caused a significantly lower miR-181b expression at 3-6 months after the intervention (p = 0.031), while no difference was observed in miR-223 and miR-126. One stent thrombosis occurred during the follow-up period. Although these technically challenging CTO-PCIs may cause enhanced platelet activation right after the intervention and long-term endothelial cell dysfunction, these interventions are not associated with more adverse clinical events.
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