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Changes in Vessel Wall Enhancement Related to the Recent Neurological Symptoms in Patients with Moyamoya Disease

Moyamoya disease (MMD) causes intracranial arterial stenosis progression. The progression of intracranial arterial stenosis will increase the risk of ischemic cerebrovascular events. This study aims to investigate the relationship between intracranial arterial stenosis progression, vessel wall enhan...

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Autores principales: MURAOKA, Shinsuke, TAOKA, Toshiaki, KAWAI, Hisashi, OKAMOTO, Sho, UDA, Kenji, NAGANAWA, Shinji, ARAKI, Yoshio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japan Neurosurgical Society 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8443970/
https://www.ncbi.nlm.nih.gov/pubmed/34078772
http://dx.doi.org/10.2176/nmc.oa.2021-0058
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author MURAOKA, Shinsuke
TAOKA, Toshiaki
KAWAI, Hisashi
OKAMOTO, Sho
UDA, Kenji
NAGANAWA, Shinji
ARAKI, Yoshio
author_facet MURAOKA, Shinsuke
TAOKA, Toshiaki
KAWAI, Hisashi
OKAMOTO, Sho
UDA, Kenji
NAGANAWA, Shinji
ARAKI, Yoshio
author_sort MURAOKA, Shinsuke
collection PubMed
description Moyamoya disease (MMD) causes intracranial arterial stenosis progression. The progression of intracranial arterial stenosis will increase the risk of ischemic cerebrovascular events. This study aims to investigate the relationship between intracranial arterial stenosis progression, vessel wall enhancement (VWE), and the recent neurological symptoms. A total of 39 MMD patients (12 male; 37.6 ± 18.0 years old) were registered in this study analysis between April 2016 and July 2018. All patients received MRI at registration and 6, 12, and 24 months post-registration. The incidence of ischemic cerebrovascular events (transit ischemic attacks or cerebral infarction) was checked until December 2018. We evaluated the relationship between the intensity of VWE, intracranial arterial stenosis, and the recent neurological symptoms. During the mean follow-up period of 13.8 ± 5.5 months, the changes in VWE were observed in 33 hemispheres (42.3%), stenosis progression was observed in 21 hemispheres (26.9%), and recent neurological symptoms occurred in 10 hemispheres (12.8%). Stenosis progression was observed in 11 hemispheres (33.3%) in the VWE(+) group and ten hemispheres (22.2%) in the VWE(−) group (p = 0.310). The recent neurological symptoms were observed in eight hemispheres (21.2%) in the VWE(+) group and two hemispheres (4.44%) in the VWE(−) group (odds ratio 6.88, 95% confidence interval 1.35–34.98, p = 0.015). The intensity of VWE sometimes changes. The changes in VWE were significantly associated with the recent neurological symptoms but not with stenosis progression.
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spelling pubmed-84439702021-09-21 Changes in Vessel Wall Enhancement Related to the Recent Neurological Symptoms in Patients with Moyamoya Disease MURAOKA, Shinsuke TAOKA, Toshiaki KAWAI, Hisashi OKAMOTO, Sho UDA, Kenji NAGANAWA, Shinji ARAKI, Yoshio Neurol Med Chir (Tokyo) Original Article Moyamoya disease (MMD) causes intracranial arterial stenosis progression. The progression of intracranial arterial stenosis will increase the risk of ischemic cerebrovascular events. This study aims to investigate the relationship between intracranial arterial stenosis progression, vessel wall enhancement (VWE), and the recent neurological symptoms. A total of 39 MMD patients (12 male; 37.6 ± 18.0 years old) were registered in this study analysis between April 2016 and July 2018. All patients received MRI at registration and 6, 12, and 24 months post-registration. The incidence of ischemic cerebrovascular events (transit ischemic attacks or cerebral infarction) was checked until December 2018. We evaluated the relationship between the intensity of VWE, intracranial arterial stenosis, and the recent neurological symptoms. During the mean follow-up period of 13.8 ± 5.5 months, the changes in VWE were observed in 33 hemispheres (42.3%), stenosis progression was observed in 21 hemispheres (26.9%), and recent neurological symptoms occurred in 10 hemispheres (12.8%). Stenosis progression was observed in 11 hemispheres (33.3%) in the VWE(+) group and ten hemispheres (22.2%) in the VWE(−) group (p = 0.310). The recent neurological symptoms were observed in eight hemispheres (21.2%) in the VWE(+) group and two hemispheres (4.44%) in the VWE(−) group (odds ratio 6.88, 95% confidence interval 1.35–34.98, p = 0.015). The intensity of VWE sometimes changes. The changes in VWE were significantly associated with the recent neurological symptoms but not with stenosis progression. The Japan Neurosurgical Society 2021-09 2021-06-03 /pmc/articles/PMC8443970/ /pubmed/34078772 http://dx.doi.org/10.2176/nmc.oa.2021-0058 Text en © 2021 The Japan Neurosurgical Society https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Original Article
MURAOKA, Shinsuke
TAOKA, Toshiaki
KAWAI, Hisashi
OKAMOTO, Sho
UDA, Kenji
NAGANAWA, Shinji
ARAKI, Yoshio
Changes in Vessel Wall Enhancement Related to the Recent Neurological Symptoms in Patients with Moyamoya Disease
title Changes in Vessel Wall Enhancement Related to the Recent Neurological Symptoms in Patients with Moyamoya Disease
title_full Changes in Vessel Wall Enhancement Related to the Recent Neurological Symptoms in Patients with Moyamoya Disease
title_fullStr Changes in Vessel Wall Enhancement Related to the Recent Neurological Symptoms in Patients with Moyamoya Disease
title_full_unstemmed Changes in Vessel Wall Enhancement Related to the Recent Neurological Symptoms in Patients with Moyamoya Disease
title_short Changes in Vessel Wall Enhancement Related to the Recent Neurological Symptoms in Patients with Moyamoya Disease
title_sort changes in vessel wall enhancement related to the recent neurological symptoms in patients with moyamoya disease
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8443970/
https://www.ncbi.nlm.nih.gov/pubmed/34078772
http://dx.doi.org/10.2176/nmc.oa.2021-0058
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