Vascular Hyperintensity on Fluid-Attenuated Inversion Recovery Indicates the Severity of Hypoperfusion in Acute Stroke.


Journal

Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association
ISSN: 1532-8511
Titre abrégé: J Stroke Cerebrovasc Dis
Pays: United States
ID NLM: 9111633

Informations de publication

Date de publication:
Feb 2020
Historique:
received: 17 07 2019
revised: 29 09 2019
accepted: 07 10 2019
pubmed: 27 11 2019
medline: 19 2 2020
entrez: 27 11 2019
Statut: ppublish

Résumé

Although fluid-attenuated inversion recovery vascular hyperintensities may be frequently seen in acute large-artery ischemic stroke, reports on their prognostic utility had been conflicting due to lack of quantitative evaluation of the perfusion status based on the signal intensity. We hypothesized that greater hyperintensity represents more severe hypoperfusion. Overall, 27 patients with acute occlusion of the proximal middle cerebral artery were divided into 2 groups, based on their signal intensity in the insular segment of middle cerebral artery on the affected side, relative to that of the insular cortex: the low signal intensity group (hypo- or isointense signals, n = 12) and the high signal intensity group (hyperintense signals, n = 15). Using dynamic susceptibility contrast magnetic resonance imaging, we assessed the time of the maximum value of the residue function and mean transit time, in the entire middle cerebral artery cortical area and diffusion-weighted imaging-Alberta Stroke Program Early Computed Tomography Score regions, including the corona radiata. The high signal intensity group had significantly longer time of the maximum value of the residue function in all the diffusion-weighted imaging-Alberta Stroke Program Early Computed Tomography Score regions, except the M3 and M6 regions, and significantly longer mean transit time in the M1 and M4 regions. Quantitative analysis of the perfusion parameters revealed more severely compromised and widely disturbed perfusion status in the high signal intensity group than in the low signal intensity group.

Sections du résumé

BACKGROUND AND AIM OBJECTIVE
Although fluid-attenuated inversion recovery vascular hyperintensities may be frequently seen in acute large-artery ischemic stroke, reports on their prognostic utility had been conflicting due to lack of quantitative evaluation of the perfusion status based on the signal intensity. We hypothesized that greater hyperintensity represents more severe hypoperfusion.
METHODS METHODS
Overall, 27 patients with acute occlusion of the proximal middle cerebral artery were divided into 2 groups, based on their signal intensity in the insular segment of middle cerebral artery on the affected side, relative to that of the insular cortex: the low signal intensity group (hypo- or isointense signals, n = 12) and the high signal intensity group (hyperintense signals, n = 15). Using dynamic susceptibility contrast magnetic resonance imaging, we assessed the time of the maximum value of the residue function and mean transit time, in the entire middle cerebral artery cortical area and diffusion-weighted imaging-Alberta Stroke Program Early Computed Tomography Score regions, including the corona radiata.
RESULTS RESULTS
The high signal intensity group had significantly longer time of the maximum value of the residue function in all the diffusion-weighted imaging-Alberta Stroke Program Early Computed Tomography Score regions, except the M3 and M6 regions, and significantly longer mean transit time in the M1 and M4 regions.
CONCLUSIONS CONCLUSIONS
Quantitative analysis of the perfusion parameters revealed more severely compromised and widely disturbed perfusion status in the high signal intensity group than in the low signal intensity group.

Identifiants

pubmed: 31767525
pii: S1052-3057(19)30550-6
doi: 10.1016/j.jstrokecerebrovasdis.2019.104467
pii:
doi:

Types de publication

Comparative Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

104467

Informations de copyright

Copyright © 2019 The Authors. Published by Elsevier Inc. All rights reserved.

Auteurs

Toshiharu Nomura (T)

Department of Neurosurgery, Brain Research Institute, University of Niigata, Chuo-ku, Niigata, Japan; Center for Integrated Brain Science, Brain Research Institute, University of Niigata, Chuo-ku, Niigata, Japan.

Kouichirou Okamoto (K)

Department of Translational Research, Brain Research Institute, University of Niigata, Chuo-ku, Niigata, Japan.

Hironaka Igarashi (H)

Center for Integrated Brain Science, Brain Research Institute, University of Niigata, Chuo-ku, Niigata, Japan.

Masato Watanabe (M)

Department of Neurosurgery, Kuwana Hospital,Higashi-ku, Niigata, Japan.

Hitoshi Hasegawa (H)

Department of Neurosurgery, Brain Research Institute, University of Niigata, Chuo-ku, Niigata, Japan.

Makoto Oishi (M)

Department of Neurosurgery, Brain Research Institute, University of Niigata, Chuo-ku, Niigata, Japan.

Yukihiko Fujii (Y)

Department of Neurosurgery, Brain Research Institute, University of Niigata, Chuo-ku, Niigata, Japan. Electronic address: yfujii@bri.niigata-u.ac.jp.

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Classifications MeSH