Endovascular biopsy in neurointerventional surgery: A systematic review

医学 活检 放射科 镊子 脑活检 血管内治疗 动脉瘤 病理 外科
作者
Oleg Shekhtman,Georgios S. Sioutas,Gennadii Piavchenko,Shubhang Bhalla,Daniel L. Cooke,Ethan A. Winkler,Jan‐Karl Burkhardt,Visish M. Srinivasan
出处
期刊:Interventional Neuroradiology [SAGE Publishing]
卷期号:32 (4): 1637-1643 被引量:5
标识
DOI:10.1177/15910199241240508
摘要

IntroductionEndothelial cells (ECs) continuously line the cerebrovasculature. Molecular aberrations in the ECs are hallmarks and contributory factors to the development of cerebrovascular diseases, including intracranial aneurysms and arteriovenous malformations (AVMs). Endovascular biopsy has been introduced as a method to harvest ECs and obtain relevant biologic information. We aimed to summarize the literature on endovascular biopsy in neurointerventional surgery.MethodsWe conducted a comprehensive literature search in multiple databases, identifying eligible studies focusing on neurosurgical applications of endovascular biopsy. The systematic review followed the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) statement. The relevant information was collected, including study characteristics, biopsy techniques, and key findings.ResultsNine studies met the inclusion criteria and were included. The studies involved the collection of ECs using various endovascular devices including coils, guide wires, different stents, and forceps. Endothelial-enrichment techniques, such fluorescence-activated cell sorting (FACS), collected ECs and facilitated downstream applications of bulk or single-cell RNA sequencing (scRNAseq). The studies provided insights into gene expression profiles and identified potential biomarkers associated with intracranial aneurysms. However, challenges were observed in obtaining an adequate number of ECs and identifying consistent biomarkers.ConclusionEndovascular biopsy of endothelial cells (ECs) in cerebrovascular pathologies shows promise for gene expression profiling. However, many studies have been limited in sample size and underpowered to identify "signature genes" for aneurysm growth or rupture. Advancements in minimally invasive biopsy methods have potential to facilitate applications of precision medicine in the treatment of cerebrovascular disorders.
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