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Endovascular Biopsy of Vertebrobasilar Aneurysm in Patient With Polyarteritis Nodosa.
Narsinh, Kazim H; Narsinh, Kamileh; McCoy, David B; Sun, Zhengda; Halabi, Cathra; Meisel, Karl; Tihan, Tarik; Chaganti, Krishna; Amans, Matthew R; Halbach, Van V; Higashida, Randall T; Hetts, Steven W; Dowd, Christopher F; Winkler, Ethan A; Abla, Adib A; Nowakowski, Tomasz J; Cooke, Daniel L.
Afiliação
  • Narsinh KH; Division of Interventional Neuroradiology, Department of Radiology and Biomedical Imaging, University of California, San Francisco, San Francisco, CA, United States.
  • Narsinh K; Division of Interventional Neuroradiology, Department of Radiology and Biomedical Imaging, University of California, San Francisco, San Francisco, CA, United States.
  • McCoy DB; Division of Interventional Neuroradiology, Department of Radiology and Biomedical Imaging, University of California, San Francisco, San Francisco, CA, United States.
  • Sun Z; Division of Interventional Neuroradiology, Department of Radiology and Biomedical Imaging, University of California, San Francisco, San Francisco, CA, United States.
  • Halabi C; Division of Neurovascular Neurology, Department of Neurology, University of California, San Francisco, San Francisco, CA, United States.
  • Meisel K; Weill Institute for Neuroscience, University of California, San Francisco, San Francisco, CA, United States.
  • Tihan T; Division of Neurovascular Neurology, Department of Neurology, University of California, San Francisco, San Francisco, CA, United States.
  • Chaganti K; Division of Neuropathology, Department of Pathology, University of California, San Francisco, San Francisco, CA, United States.
  • Amans MR; Division of Rheumatology, Department of Medicine, University of California, San Francisco, San Francisco, CA, United States.
  • Halbach VV; Division of Interventional Neuroradiology, Department of Radiology and Biomedical Imaging, University of California, San Francisco, San Francisco, CA, United States.
  • Higashida RT; Division of Interventional Neuroradiology, Department of Radiology and Biomedical Imaging, University of California, San Francisco, San Francisco, CA, United States.
  • Hetts SW; Division of Interventional Neuroradiology, Department of Radiology and Biomedical Imaging, University of California, San Francisco, San Francisco, CA, United States.
  • Dowd CF; Division of Interventional Neuroradiology, Department of Radiology and Biomedical Imaging, University of California, San Francisco, San Francisco, CA, United States.
  • Winkler EA; Division of Interventional Neuroradiology, Department of Radiology and Biomedical Imaging, University of California, San Francisco, San Francisco, CA, United States.
  • Abla AA; Cerebrovascular Disorders Program, Department of Neurological Surgery, University of California, San Francisco, San Francisco, CA, United States.
  • Nowakowski TJ; Cerebrovascular Disorders Program, Department of Neurological Surgery, University of California, San Francisco, San Francisco, CA, United States.
  • Cooke DL; Department of Anatomy, Chan Zuckerberg Biohub, University of California, San Francisco, San Francisco, CA, United States.
Front Neurol ; 12: 697105, 2021.
Article em En | MEDLINE | ID: mdl-34887823
ABSTRACT
Background and

Purpose:

The management of unruptured intracranial aneurysms remains controversial. The decisions to treat are heavily informed by estimated risk of bleeding. However, these estimates are imprecise, and better methods for stratifying the risk or tailoring treatment strategy are badly needed. Here, we demonstrate an initial proof-of-principle concept for endovascular biopsy to identify the key molecular pathways and gene expression changes associated with aneurysm formation. We couple this technique with single cell RNA sequencing (scRNAseq) to develop a roadmap of the pathogenic changes of a dolichoectatic vertebrobasilar aneurysm in a patient with polyarteritis nodosa.

Methods:

Endovascular biopsy and fluorescence activated cell sorting was used to isolate the viable endothelial cells (ECs) using the established techniques. A single cell RNA sequencing (scRNAseq) was then performed on 24 aneurysmal ECs and 23 patient-matched non-aneurysmal ECs. An integrated panel of bioinformatic tools was applied to determine the differential gene expression, enriched signaling pathways, and cell subpopulations hypothesized to drive disease pathogenesis.

Results:

We identify a subset of 7 (29%) aneurysm-specific ECs with a distinct gene expression signature not found in the patient-matched control ECs. A gene set enrichment analysis identified these ECs to have increased the expression of genes regulating the leukocyte-endothelial cell adhesion, major histocompatibility complex (MHC) class I, T cell receptor recycling, tumor necrosis factor alpha (TNFα) response, and interferon gamma signaling. A histopathologic analysis of a different intracranial aneurysm that was later resected yielded a diagnosis of polyarteritis nodosa and positive staining for TNFα.

Conclusions:

We demonstrate feasibility of applying scRNAseq to the endovascular biopsy samples and identify a subpopulation of ECs associated with cerebral aneurysm in polyarteritis nodosa. Endovascular biopsy may be a safe method for deriving insight into the disease pathogenesis and tailoring the personalized treatment approaches to intracranial aneurysms.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article