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Deep learning reveals disease-specific signatures of white matter pathology in tauopathies

Although pathology of tauopathies is characterized by abnormal tau protein aggregation in both gray and white matter regions of the brain, neuropathological investigations have generally focused on abnormalities in the cerebral cortex because the canonical aggregates that form the diagnostic criteri...

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Autores principales: Vega, Anthony R., Chkheidze, Rati, Jarmale, Vipul, Shang, Ping, Foong, Chan, Diamond, Marc I., White, Charles L., Rajaram, Satwik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8529809/
https://www.ncbi.nlm.nih.gov/pubmed/34674762
http://dx.doi.org/10.1186/s40478-021-01271-x
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author Vega, Anthony R.
Chkheidze, Rati
Jarmale, Vipul
Shang, Ping
Foong, Chan
Diamond, Marc I.
White, Charles L.
Rajaram, Satwik
author_facet Vega, Anthony R.
Chkheidze, Rati
Jarmale, Vipul
Shang, Ping
Foong, Chan
Diamond, Marc I.
White, Charles L.
Rajaram, Satwik
author_sort Vega, Anthony R.
collection PubMed
description Although pathology of tauopathies is characterized by abnormal tau protein aggregation in both gray and white matter regions of the brain, neuropathological investigations have generally focused on abnormalities in the cerebral cortex because the canonical aggregates that form the diagnostic criteria for these disorders predominate there. This corticocentric focus tends to deemphasize the relevance of the more complex white matter pathologies, which remain less well characterized and understood. We took a data-driven machine-learning approach to identify novel disease-specific morphologic signatures of white matter aggregates in three tauopathies: Alzheimer disease (AD), progressive supranuclear palsy (PSP), and corticobasal degeneration (CBD). We developed automated approaches using whole slide images of tau immunostained sections from 49 human autopsy brains (16 AD,13 CBD, 20 PSP) to identify cortex/white matter regions and individual tau aggregates, and compared tau-aggregate morphology across these diseases. Tau burden in the gray and white matter for individual subjects strongly correlated in a highly disease-specific fashion. We discovered previously unrecognized tau morphologies for AD, CBD and PSP that may be of importance in disease classification. Intriguingly, our models classified diseases equally well based on either white or gray matter tau staining. Our results suggest that tau pathology in white matter is informative, disease-specific, and linked to gray matter pathology. Machine learning has the potential to reveal latent information in histologic images that may represent previously unrecognized patterns of neuropathology, and additional studies of tau pathology in white matter could improve diagnostic accuracy. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40478-021-01271-x.
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spelling pubmed-85298092021-10-25 Deep learning reveals disease-specific signatures of white matter pathology in tauopathies Vega, Anthony R. Chkheidze, Rati Jarmale, Vipul Shang, Ping Foong, Chan Diamond, Marc I. White, Charles L. Rajaram, Satwik Acta Neuropathol Commun Research Although pathology of tauopathies is characterized by abnormal tau protein aggregation in both gray and white matter regions of the brain, neuropathological investigations have generally focused on abnormalities in the cerebral cortex because the canonical aggregates that form the diagnostic criteria for these disorders predominate there. This corticocentric focus tends to deemphasize the relevance of the more complex white matter pathologies, which remain less well characterized and understood. We took a data-driven machine-learning approach to identify novel disease-specific morphologic signatures of white matter aggregates in three tauopathies: Alzheimer disease (AD), progressive supranuclear palsy (PSP), and corticobasal degeneration (CBD). We developed automated approaches using whole slide images of tau immunostained sections from 49 human autopsy brains (16 AD,13 CBD, 20 PSP) to identify cortex/white matter regions and individual tau aggregates, and compared tau-aggregate morphology across these diseases. Tau burden in the gray and white matter for individual subjects strongly correlated in a highly disease-specific fashion. We discovered previously unrecognized tau morphologies for AD, CBD and PSP that may be of importance in disease classification. Intriguingly, our models classified diseases equally well based on either white or gray matter tau staining. Our results suggest that tau pathology in white matter is informative, disease-specific, and linked to gray matter pathology. Machine learning has the potential to reveal latent information in histologic images that may represent previously unrecognized patterns of neuropathology, and additional studies of tau pathology in white matter could improve diagnostic accuracy. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40478-021-01271-x. BioMed Central 2021-10-21 /pmc/articles/PMC8529809/ /pubmed/34674762 http://dx.doi.org/10.1186/s40478-021-01271-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Vega, Anthony R.
Chkheidze, Rati
Jarmale, Vipul
Shang, Ping
Foong, Chan
Diamond, Marc I.
White, Charles L.
Rajaram, Satwik
Deep learning reveals disease-specific signatures of white matter pathology in tauopathies
title Deep learning reveals disease-specific signatures of white matter pathology in tauopathies
title_full Deep learning reveals disease-specific signatures of white matter pathology in tauopathies
title_fullStr Deep learning reveals disease-specific signatures of white matter pathology in tauopathies
title_full_unstemmed Deep learning reveals disease-specific signatures of white matter pathology in tauopathies
title_short Deep learning reveals disease-specific signatures of white matter pathology in tauopathies
title_sort deep learning reveals disease-specific signatures of white matter pathology in tauopathies
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8529809/
https://www.ncbi.nlm.nih.gov/pubmed/34674762
http://dx.doi.org/10.1186/s40478-021-01271-x
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