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Published on: March 16, 2022
Endovascular treatment of unruptured intracranial aneurysms and circulating endothelial cells
Jean-François Vendrell1, Renaud Cezar, Nils Kuster
1Department of Neuroradiology, University Hospital Center, Guy de Chauliac Hospital, 80 Avenue Augustin Fliche, 34295 Montpellier Cedex, France. jfvendrell@yahoo.fr
Insights
Endovascular treatment (EVT) of brain aneurysms releases circulating endothelial cells (CECs), potentially causing silent ischemic brain lesions. Monitoring CECs may help optimize EVT and reduce complications.
Area of Science:
- Neuroendovascular research
- Vascular biology
- Medical device technology
Background:
- Endovascular treatment (EVT) is a common procedure for unruptured intracranial aneurysms.
- Complications, such as silent ischemic brain lesions, can occur despite successful treatment.
- Circulating endothelial cells (CECs) are shed from damaged blood vessel walls.
Purpose of the Study:
- To investigate the role of CECs in complications following EVT for intracranial aneurysms.
- To characterize and quantify CECs in different blood compartments before and after EVT.
- To correlate CEC levels with the occurrence of ischemic brain events.
Main Methods:
- CECs were identified and counted using the CellTracks(®) System in blood samples from the femoral artery, internal carotid artery (before and after EVT), and peripheral veins (before and after EVT).
- Patients (n=15) underwent diffusion-weighted imaging (DWI-MRI) to assess ischemic brain lesions before and 24 hours after EVT.
- CEC characterization involved markers CD146, CD105, CD45, and DAPI.
Main Results:
- Higher numbers of single CECs and clusters were found in the internal carotid artery (ICA) before EVT compared to other sampling sites.
- Large CEC clusters were predominantly observed in the ICA, suggesting device-induced endothelial injury.
- Silent ischemic brain lesions were detected in 60% (9/15) of patients, despite uneventful clinical recovery.
Conclusions:
- EVT procedures can lead to the detachment of CECs from arterial walls, potentially contributing to the formation of silent ischemic brain lesions.
- Quantifying CECs alongside DWI-MRI may offer a valuable method for monitoring EVT outcomes and refining endovascular device strategies.
- This approach could help minimize EVT-related complications.
Objectives:
To evaluate the potential implication of circulating endothelial cells (CECs) in complications following endovascular treatment (EVT) of unruptured intracranial aneurysms. CECs characterized as CD146(+)/CD105(+)/CD45(-)/DAPI(+) were considered to originate from an altered endothelial cell layer of the vessel wall.
Study Design:
In 15 patients, CECs were characterized and enumerated by the CellTracks(®) System in blood samples from: (1) femoral artery (FA), (2) internal carotid artery (ICA) before (ICA1) and after procedure (ICA2), and (3) a peripheral vein before (PV1) and after EVT (PV2). Ischemic brain events were assessed using diffusion weighted imaging (DWI-MRI) before and 24h after EVT.
Results:
In ICA1, the median number of single CECs and clusters of 2-5 CECs were higher than in FA, ICA2, PV1 and PV2 samples (P<0.001). Clusters >5 cells, sometimes >50μm, were mainly observed in ICA1 and never in PV1, PV2 or PV samples from ten healthy subjects. This distribution of CECs suggested femoral and ICA injury by the devices used, leading to endothelium shearing and desquamation of CECs. All patients discharged on day two (NIHSS score=0), however silent ischemic brain lesions were observed in 9/15 (60%).
Conclusions:
EVT detaches single and clusters of CECs from wall arteries that may be implicated in silent ischemic brain lesions genesis. Enumeration of CECs associated with DWI-MRI might represent an interesting strategy for monitoring and optimizing endovascular devices, and further limit EVT-related complications.
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