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Myelin damage and cortical atrophy in watershed regions in patients with moyamoya angiopathy. / Filimonova, Elena; Ovsiannikov, Konstantin; Sosnov, Alexsey et al.

In: Frontiers in Neuroscience, Vol. 16, 982829, 23.08.2022.

Research output: Contribution to journalArticlepeer-review

Harvard

Filimonova, E, Ovsiannikov, K, Sosnov, A, Perfilyev, A, Gafurov, R, Galaktionov, D, Bervickiy, A, Kiselev, V & Rzaev, J 2022, 'Myelin damage and cortical atrophy in watershed regions in patients with moyamoya angiopathy', Frontiers in Neuroscience, vol. 16, 982829. https://doi.org/10.3389/fnins.2022.982829

APA

Filimonova, E., Ovsiannikov, K., Sosnov, A., Perfilyev, A., Gafurov, R., Galaktionov, D., Bervickiy, A., Kiselev, V., & Rzaev, J. (2022). Myelin damage and cortical atrophy in watershed regions in patients with moyamoya angiopathy. Frontiers in Neuroscience, 16, [982829]. https://doi.org/10.3389/fnins.2022.982829

Vancouver

Filimonova E, Ovsiannikov K, Sosnov A, Perfilyev A, Gafurov R, Galaktionov D et al. Myelin damage and cortical atrophy in watershed regions in patients with moyamoya angiopathy. Frontiers in Neuroscience. 2022 Aug 23;16:982829. doi: 10.3389/fnins.2022.982829

Author

Filimonova, Elena ; Ovsiannikov, Konstantin ; Sosnov, Alexsey et al. / Myelin damage and cortical atrophy in watershed regions in patients with moyamoya angiopathy. In: Frontiers in Neuroscience. 2022 ; Vol. 16.

BibTeX

@article{2326c3b2861b4e48bd534798a9b7ef8f,
title = "Myelin damage and cortical atrophy in watershed regions in patients with moyamoya angiopathy",
abstract = "Background: Despite it being known that chronic ischemia results in myelin damage and gray matter atrophy, data regarding patients with moyamoya angiopathy is limited. We hypothesized that chronic ischemia in moyamoya angiopathy leads to myelin damage, especially in anterior watershed regions, as well as cortical atrophy in these areas. Materials and methods: Twenty adult patients with moyamoya angiopathy and 17 age- and sex-matched healthy controls were evaluated using the T1w/T2w mapping method and surface-based MR-morphometry. The T1w/T2w signal intensity ratio, which reflects the white matter integrity, and the cortical thickness, were calculated in watershed regions and compared between the patients and controls. In the patients with moyamoya angiopathy, the correlations between these parameters and the Suzuki stage were also evaluated. Results: The regional T1w/T2w ratio values from centrum semiovale in patients with MMA were significantly lower than those in healthy controls (p < 0.05); there was also a downward trend in T1w/T2w ratio values from middle frontal gyrus white matter in patients compared with the controls (p < 0.1). The cortical thickness of the middle frontal gyrus was significantly lower in patients than in healthy controls (p < 0.05). There were negative correlations between the Suzuki stage and the T1w/T2w ratio values from the centrum semiovale and middle frontal white matter. Conclusion: T1w/T2w mapping revealed that myelin damage exists in watershed regions in patients with moyamoya angiopathy, in association with cortical atrophy according to MR-morphometry. These changes were correlated with the disease stage.",
keywords = "demyelination, FreeSurfer, magnetic resonance imaging (MRI), moyamoya angiopathy (MMA), MR-morphometry, T1w/T2w ratio",
author = "Elena Filimonova and Konstantin Ovsiannikov and Alexsey Sosnov and Artem Perfilyev and Rustam Gafurov and Dmitriy Galaktionov and Anatoliy Bervickiy and Vitaly Kiselev and Jamil Rzaev",
note = "Publisher Copyright: Copyright {\textcopyright} 2022 Filimonova, Ovsiannikov, Sosnov, Perfilyev, Gafurov, Galaktionov, Bervickiy, Kiselev and Rzaev.",
year = "2022",
month = aug,
day = "23",
doi = "10.3389/fnins.2022.982829",
language = "English",
volume = "16",
journal = "Frontiers in Neuroscience",
issn = "1662-4548",
publisher = "Frontiers Media S.A.",

}

RIS

TY - JOUR

T1 - Myelin damage and cortical atrophy in watershed regions in patients with moyamoya angiopathy

AU - Filimonova, Elena

AU - Ovsiannikov, Konstantin

AU - Sosnov, Alexsey

AU - Perfilyev, Artem

AU - Gafurov, Rustam

AU - Galaktionov, Dmitriy

AU - Bervickiy, Anatoliy

AU - Kiselev, Vitaly

AU - Rzaev, Jamil

N1 - Publisher Copyright: Copyright © 2022 Filimonova, Ovsiannikov, Sosnov, Perfilyev, Gafurov, Galaktionov, Bervickiy, Kiselev and Rzaev.

PY - 2022/8/23

Y1 - 2022/8/23

N2 - Background: Despite it being known that chronic ischemia results in myelin damage and gray matter atrophy, data regarding patients with moyamoya angiopathy is limited. We hypothesized that chronic ischemia in moyamoya angiopathy leads to myelin damage, especially in anterior watershed regions, as well as cortical atrophy in these areas. Materials and methods: Twenty adult patients with moyamoya angiopathy and 17 age- and sex-matched healthy controls were evaluated using the T1w/T2w mapping method and surface-based MR-morphometry. The T1w/T2w signal intensity ratio, which reflects the white matter integrity, and the cortical thickness, were calculated in watershed regions and compared between the patients and controls. In the patients with moyamoya angiopathy, the correlations between these parameters and the Suzuki stage were also evaluated. Results: The regional T1w/T2w ratio values from centrum semiovale in patients with MMA were significantly lower than those in healthy controls (p < 0.05); there was also a downward trend in T1w/T2w ratio values from middle frontal gyrus white matter in patients compared with the controls (p < 0.1). The cortical thickness of the middle frontal gyrus was significantly lower in patients than in healthy controls (p < 0.05). There were negative correlations between the Suzuki stage and the T1w/T2w ratio values from the centrum semiovale and middle frontal white matter. Conclusion: T1w/T2w mapping revealed that myelin damage exists in watershed regions in patients with moyamoya angiopathy, in association with cortical atrophy according to MR-morphometry. These changes were correlated with the disease stage.

AB - Background: Despite it being known that chronic ischemia results in myelin damage and gray matter atrophy, data regarding patients with moyamoya angiopathy is limited. We hypothesized that chronic ischemia in moyamoya angiopathy leads to myelin damage, especially in anterior watershed regions, as well as cortical atrophy in these areas. Materials and methods: Twenty adult patients with moyamoya angiopathy and 17 age- and sex-matched healthy controls were evaluated using the T1w/T2w mapping method and surface-based MR-morphometry. The T1w/T2w signal intensity ratio, which reflects the white matter integrity, and the cortical thickness, were calculated in watershed regions and compared between the patients and controls. In the patients with moyamoya angiopathy, the correlations between these parameters and the Suzuki stage were also evaluated. Results: The regional T1w/T2w ratio values from centrum semiovale in patients with MMA were significantly lower than those in healthy controls (p < 0.05); there was also a downward trend in T1w/T2w ratio values from middle frontal gyrus white matter in patients compared with the controls (p < 0.1). The cortical thickness of the middle frontal gyrus was significantly lower in patients than in healthy controls (p < 0.05). There were negative correlations between the Suzuki stage and the T1w/T2w ratio values from the centrum semiovale and middle frontal white matter. Conclusion: T1w/T2w mapping revealed that myelin damage exists in watershed regions in patients with moyamoya angiopathy, in association with cortical atrophy according to MR-morphometry. These changes were correlated with the disease stage.

KW - demyelination

KW - FreeSurfer

KW - magnetic resonance imaging (MRI)

KW - moyamoya angiopathy (MMA)

KW - MR-morphometry

KW - T1w/T2w ratio

UR - http://www.scopus.com/inward/record.url?scp=85137997659&partnerID=8YFLogxK

UR - https://www.mendeley.com/catalogue/a5c5f68a-2fb2-3250-a7bb-d05207bb4ce9/

U2 - 10.3389/fnins.2022.982829

DO - 10.3389/fnins.2022.982829

M3 - Article

C2 - 36081657

AN - SCOPUS:85137997659

VL - 16

JO - Frontiers in Neuroscience

JF - Frontiers in Neuroscience

SN - 1662-4548

M1 - 982829

ER -

ID: 38050430