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Postmortem 7T MRI for guided histopathology and evaluation of cerebrovascular disease

Postmortem (PM) magnetic resonance imaging (MRI) can serve as a bridge between in vivo imaging and histology by connecting MRI observed macrostructural findings to histological staining and microstructural changes. Data were acquired from 20 formalin-fixed brains including T2, T1, PD, and T2*-weight...

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Autores principales: Lahna, David, Roese, Natalie, Woltjer, Randy, Boespflug, Erin L, Schwartz, Daniel, Grinstead, John, Dodge, Hiroko H, Wall, Rachel, Kaye, Jeffrey A, Rooney, William D, Silbert, Lisa C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9764082/
https://www.ncbi.nlm.nih.gov/pubmed/36343095
http://dx.doi.org/10.1093/jnen/nlac103
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author Lahna, David
Roese, Natalie
Woltjer, Randy
Boespflug, Erin L
Schwartz, Daniel
Grinstead, John
Dodge, Hiroko H
Wall, Rachel
Kaye, Jeffrey A
Rooney, William D
Silbert, Lisa C
author_facet Lahna, David
Roese, Natalie
Woltjer, Randy
Boespflug, Erin L
Schwartz, Daniel
Grinstead, John
Dodge, Hiroko H
Wall, Rachel
Kaye, Jeffrey A
Rooney, William D
Silbert, Lisa C
author_sort Lahna, David
collection PubMed
description Postmortem (PM) magnetic resonance imaging (MRI) can serve as a bridge between in vivo imaging and histology by connecting MRI observed macrostructural findings to histological staining and microstructural changes. Data were acquired from 20 formalin-fixed brains including T2, T1, PD, and T2*-weighted images of left hemispheres and 6-mm-thick coronal slices. Tissue slices were bisected, aligned to MR images and used to guide histological sampling. Markers of myelin and oligodendroglia alterations were semiquantitatively rated and compared within white matter hyperintensities (WMHs) and normal-appearing white matter. Tissue priors were created from 3T in vivo data and used to guide segmentation of WMH. PM WMH and hemisphere volumes were compared to volumes derived from in vivo data. PM T2 WMH and T1 hemisphere volumes were correlated with in vivo 3T FLAIR WMH and T1 hemisphere volumes. WMH showed significant myelin loss, decreased GFAP expression and increased vimentin expression. MR-visible perivascular spaces and cortical microvascular lesions were successfully captured on histopathological sections. PM MRI can quantify cerebrovascular disease burden and guide tissue sampling, allowing for more comprehensive characterization of cerebrovascular disease that may be used to study etiologies of age-related cognitive change.
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spelling pubmed-97640822022-12-20 Postmortem 7T MRI for guided histopathology and evaluation of cerebrovascular disease Lahna, David Roese, Natalie Woltjer, Randy Boespflug, Erin L Schwartz, Daniel Grinstead, John Dodge, Hiroko H Wall, Rachel Kaye, Jeffrey A Rooney, William D Silbert, Lisa C J Neuropathol Exp Neurol Original Article Postmortem (PM) magnetic resonance imaging (MRI) can serve as a bridge between in vivo imaging and histology by connecting MRI observed macrostructural findings to histological staining and microstructural changes. Data were acquired from 20 formalin-fixed brains including T2, T1, PD, and T2*-weighted images of left hemispheres and 6-mm-thick coronal slices. Tissue slices were bisected, aligned to MR images and used to guide histological sampling. Markers of myelin and oligodendroglia alterations were semiquantitatively rated and compared within white matter hyperintensities (WMHs) and normal-appearing white matter. Tissue priors were created from 3T in vivo data and used to guide segmentation of WMH. PM WMH and hemisphere volumes were compared to volumes derived from in vivo data. PM T2 WMH and T1 hemisphere volumes were correlated with in vivo 3T FLAIR WMH and T1 hemisphere volumes. WMH showed significant myelin loss, decreased GFAP expression and increased vimentin expression. MR-visible perivascular spaces and cortical microvascular lesions were successfully captured on histopathological sections. PM MRI can quantify cerebrovascular disease burden and guide tissue sampling, allowing for more comprehensive characterization of cerebrovascular disease that may be used to study etiologies of age-related cognitive change. Oxford University Press 2022-11-07 /pmc/articles/PMC9764082/ /pubmed/36343095 http://dx.doi.org/10.1093/jnen/nlac103 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of American Association of Neuropathologists, Inc. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Original Article
Lahna, David
Roese, Natalie
Woltjer, Randy
Boespflug, Erin L
Schwartz, Daniel
Grinstead, John
Dodge, Hiroko H
Wall, Rachel
Kaye, Jeffrey A
Rooney, William D
Silbert, Lisa C
Postmortem 7T MRI for guided histopathology and evaluation of cerebrovascular disease
title Postmortem 7T MRI for guided histopathology and evaluation of cerebrovascular disease
title_full Postmortem 7T MRI for guided histopathology and evaluation of cerebrovascular disease
title_fullStr Postmortem 7T MRI for guided histopathology and evaluation of cerebrovascular disease
title_full_unstemmed Postmortem 7T MRI for guided histopathology and evaluation of cerebrovascular disease
title_short Postmortem 7T MRI for guided histopathology and evaluation of cerebrovascular disease
title_sort postmortem 7t mri for guided histopathology and evaluation of cerebrovascular disease
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9764082/
https://www.ncbi.nlm.nih.gov/pubmed/36343095
http://dx.doi.org/10.1093/jnen/nlac103
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