Insights into the pathogenesis of cerebral fusiform aneurysms: high-resolution MRI and computational analysis.


Journal

Journal of neurointerventional surgery
ISSN: 1759-8486
Titre abrégé: J Neurointerv Surg
Pays: England
ID NLM: 101517079

Informations de publication

Date de publication:
Dec 2021
Historique:
received: 23 12 2020
revised: 26 01 2021
accepted: 29 01 2021
pubmed: 27 2 2021
medline: 23 11 2021
entrez: 26 2 2021
Statut: ppublish

Résumé

Intracranial fusiform aneurysms are complex and poorly characterized vascular lesions. High-resolution magnetic resonance imaging (HR-MRI) and computational morphological analysis may be used to characterize cerebral fusiform aneurysms. To use advanced imaging and computational analysis to understand the unique pathophysiology, and determine possible underlying mechanisms of instability of cerebral fusiform aneurysms. Patients with unruptured intracranial aneurysms prospectively underwent imaging with 3T HR-MRI at diagnosis. Aneurysmal wall enhancement was objectively quantified using signal intensity after normalization of the contrast ratio (CR) with the pituitary stalk. Enhancement between saccular and fusiform aneurysms was compared, as well as enhancement characteristics of fusiform aneurysms. The presence of microhemorrhages in fusiform aneurysms was determined with quantitative susceptibility mapping (QSM). Three distinct types of fusiform aneurysms were analyzed with computational fluid dynamics (CFD) and finite element analysis (FEA). A total of 130 patients with 160 aneurysms underwent HR-MRI. 136 aneurysms were saccular and 24 were fusiform. Fusiform aneurysms had a significantly higher CR and diameter than saccular aneurysms. Enhancing fusiform aneurysms exhibited more enhancement of reference vessels than non-enhancing fusiform aneurysms. Ten fusiform aneurysms underwent QSM analysis, and five aneurysms showed microhemorrhages. Microhemorrhage-positive aneurysms had a larger volume, diameter, and greater enhancement than aneurysms without microhemorrhage. Three types of fusiform aneurysms exhibited different CFD and FEA patterns. Fusiform aneurysms exhibited more contrast enhancement than saccular aneurysms. Enhancing fusiform aneurysms had larger volume and diameter, more enhancement of reference vessels, and more often exhibited microhemorrhage than non-enhancing aneurysms. CFD and FEA suggest that various pathophysiological processes determine the formation and growth of fusiform aneurysms.

Sections du résumé

BACKGROUND BACKGROUND
Intracranial fusiform aneurysms are complex and poorly characterized vascular lesions. High-resolution magnetic resonance imaging (HR-MRI) and computational morphological analysis may be used to characterize cerebral fusiform aneurysms.
OBJECTIVE OBJECTIVE
To use advanced imaging and computational analysis to understand the unique pathophysiology, and determine possible underlying mechanisms of instability of cerebral fusiform aneurysms.
METHODS METHODS
Patients with unruptured intracranial aneurysms prospectively underwent imaging with 3T HR-MRI at diagnosis. Aneurysmal wall enhancement was objectively quantified using signal intensity after normalization of the contrast ratio (CR) with the pituitary stalk. Enhancement between saccular and fusiform aneurysms was compared, as well as enhancement characteristics of fusiform aneurysms. The presence of microhemorrhages in fusiform aneurysms was determined with quantitative susceptibility mapping (QSM). Three distinct types of fusiform aneurysms were analyzed with computational fluid dynamics (CFD) and finite element analysis (FEA).
RESULTS RESULTS
A total of 130 patients with 160 aneurysms underwent HR-MRI. 136 aneurysms were saccular and 24 were fusiform. Fusiform aneurysms had a significantly higher CR and diameter than saccular aneurysms. Enhancing fusiform aneurysms exhibited more enhancement of reference vessels than non-enhancing fusiform aneurysms. Ten fusiform aneurysms underwent QSM analysis, and five aneurysms showed microhemorrhages. Microhemorrhage-positive aneurysms had a larger volume, diameter, and greater enhancement than aneurysms without microhemorrhage. Three types of fusiform aneurysms exhibited different CFD and FEA patterns.
CONCLUSION CONCLUSIONS
Fusiform aneurysms exhibited more contrast enhancement than saccular aneurysms. Enhancing fusiform aneurysms had larger volume and diameter, more enhancement of reference vessels, and more often exhibited microhemorrhage than non-enhancing aneurysms. CFD and FEA suggest that various pathophysiological processes determine the formation and growth of fusiform aneurysms.

Identifiants

pubmed: 33632878
pii: neurintsurg-2020-017243
doi: 10.1136/neurintsurg-2020-017243
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1180-1186

Informations de copyright

© Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

Auteurs

Ryan Phillip Sabotin (RP)

Department of Neurology, The University of Iowa Hospitals and Clinics, Iowa City, Iowa, USA.

Alberto Varon (A)

Department of Neurology, The University of Iowa, Iowa City, Iowa, USA.

Jorge A Roa (JA)

Department of Neurology, The University of Iowa Hospitals and Clinics, Iowa City, Iowa, USA.

Ashrita Raghuram (A)

Department of Neurology, The University of Iowa Hospitals and Clinics, Iowa City, Iowa, USA.

Daizo Ishii (D)

Department of Neurosurgery, The University of Iowa Hospitals and Clinics, Iowa City, Iowa, USA.

Marco Nino (M)

Roy J Carver Department of Biomedical Engineering, The University of Iowa, Iowa City, Iowa, USA.

Adam E Galloy (AE)

Roy J Carver Department of Biomedical Engineering, The University of Iowa, Iowa City, Iowa, USA.

Devanshee Patel (D)

Department of Neurology, The University of Iowa Hospitals and Clinics, Iowa City, Iowa, USA.

Madhavan L Raghavan (ML)

Roy J Carver Department of Biomedical Engineering, The University of Iowa, Iowa City, Iowa, USA.

David Hasan (D)

Department of Neurosurgery, The University of Iowa Hospitals and Clinics, Iowa City, Iowa, USA.

Edgar A Samaniego (EA)

Department of Neurology, The University of Iowa Hospitals and Clinics, Iowa City, Iowa, USA edgarsama@gmail.com.
Department of Neurosurgery, The University of Iowa Hospitals and Clinics, Iowa City, Iowa, USA.
Department of Radiology, The University of Iowa Hospitals and Clinics, Iowa City, Iowa, USA.

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