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Published on: September 22, 2020
Effects of percutaneous coronary intervention on peripheral venous blood circulating endothelial cells and plasma
Christopher J Boos1, Balu Balakrishnan, Shahirose Jessani
1Haemostasis, Thrombosis and Vascular Biology Unit, University Department of Medicine, City Hospital, Birmingham B18 7QH, UK.
Insights
Percutaneous coronary intervention (PCI) significantly increases markers of endothelial damage, including circulating endothelial cells (CECs), von Willebrand factor (vWF), and soluble E-selectin (sEsel). Diagnostic coronary angiography (CA) did not show these effects, indicating PCI causes endothelial dysfunction.
Area of Science:
- Cardiovascular Medicine
- Interventional Cardiology
- Endothelial Biology
Background:
- Endothelial damage/dysfunction is linked to coronary artery disease.
- The impact of percutaneous coronary intervention (PCI) on endothelial damage markers is not fully understood.
- Key markers include circulating endothelial cells (CECs), von Willebrand factor (vWF), and soluble E-selectin (sEsel).
Purpose of the Study:
- To evaluate the effects of diagnostic coronary angiography (CA) and PCI on CECs, vWF, and sEsel levels.
- To compare baseline levels of these markers in patients and healthy controls.
Main Methods:
- Blood samples were collected before and after CA (n=15).
- Blood samples were collected before, 15 minutes after, and 24 hours after PCI (n=38).
- Levels of CECs, vWF, and sEsel were measured in patients undergoing CA, PCI, and in healthy controls.
Main Results:
- No significant differences in baseline endothelial marker levels were found between healthy controls, CA, and PCI groups.
- CA did not significantly alter vWF or CEC levels.
- PCI led to significant increases in CECs, vWF, and sEsel at 15 minutes and 24 hours post-procedure compared to pre-PCI levels.
Conclusions:
- Elective PCI causes significant increases in circulating endothelial cells, von Willebrand factor, and soluble E-selectin.
- Diagnostic coronary angiography does not appear to induce similar changes in these endothelial markers.
- The observed increases suggest endothelial damage or dysfunction following PCI.
Background:
The relationship between endothelial damage/dysfunction and coronary artery disease is well recognized. However, the effects of percutaneous coronary intervention (PCI) [stenting/angioplasty] on circulating markers of endothelial damage/dysfunction (eg, von Willebrand factor [vWF], soluble E-selectin [sEsel] levels, and more recently circulating endothelial cells [CECs]) has been less well defined.
Aims And Methods:
We investigated the effects of both diagnostic coronary angiography (CA) [n = 15; blood sampling immediately before CA and 15 min after CA] and PCI (n = 38; blood sampling before PCI, 15 min after PCI, and 24 h after PCI) on levels of CECs, vWF, and sEsel across comparable patient groups. We also included a cohort of comparable healthy control subjects in order to compare baseline levels of three endothelial markers.
Results:
There were no differences in baseline levels of CECs, vWF, or sEsel between the three study groups (healthy control subjects, CA, PCI; all p = not significant). Following CA (before to 15 min after), there were no significant changes in vWF and CECs (p = not significant). Following PCI, there were significant increases observed at 15 min after PCI and at 24 h after PCI (when compared with pre-PCI levels) in CECs (p = 0.0006), vWF (p = 0.007), and sEsel (p = 0.024).
Conclusion:
We observed significant increases in three endothelial markers (CECs, vWF, and sEsel) with elective PCI but not CA. This is in keeping with endothelial damage/dysfunction following PCI.
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