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Interpretable classification of Alzheimer’s disease pathologies with a convolutional neural network pipeline
Neuropathologists assess vast brain areas to identify diverse and subtly-differentiated morphologies. Standard semi-quantitative scoring approaches, however, are coarse-grained and lack precise neuroanatomic localization. We report a proof-of-concept deep learning pipeline that identifies specific n...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6520374/ https://www.ncbi.nlm.nih.gov/pubmed/31092819 http://dx.doi.org/10.1038/s41467-019-10212-1 |
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author | Tang, Ziqi Chuang, Kangway V. DeCarli, Charles Jin, Lee-Way Beckett, Laurel Keiser, Michael J. Dugger, Brittany N. |
author_facet | Tang, Ziqi Chuang, Kangway V. DeCarli, Charles Jin, Lee-Way Beckett, Laurel Keiser, Michael J. Dugger, Brittany N. |
author_sort | Tang, Ziqi |
collection | PubMed |
description | Neuropathologists assess vast brain areas to identify diverse and subtly-differentiated morphologies. Standard semi-quantitative scoring approaches, however, are coarse-grained and lack precise neuroanatomic localization. We report a proof-of-concept deep learning pipeline that identifies specific neuropathologies—amyloid plaques and cerebral amyloid angiopathy—in immunohistochemically-stained archival slides. Using automated segmentation of stained objects and a cloud-based interface, we annotate > 70,000 plaque candidates from 43 whole slide images (WSIs) to train and evaluate convolutional neural networks. Networks achieve strong plaque classification on a 10-WSI hold-out set (0.993 and 0.743 areas under the receiver operating characteristic and precision recall curve, respectively). Prediction confidence maps visualize morphology distributions at high resolution. Resulting network-derived amyloid beta (Aβ)-burden scores correlate well with established semi-quantitative scores on a 30-WSI blinded hold-out. Finally, saliency mapping demonstrates that networks learn patterns agreeing with accepted pathologic features. This scalable means to augment a neuropathologist’s ability suggests a route to neuropathologic deep phenotyping. |
format | Online Article Text |
id | pubmed-6520374 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-65203742019-05-20 Interpretable classification of Alzheimer’s disease pathologies with a convolutional neural network pipeline Tang, Ziqi Chuang, Kangway V. DeCarli, Charles Jin, Lee-Way Beckett, Laurel Keiser, Michael J. Dugger, Brittany N. Nat Commun Article Neuropathologists assess vast brain areas to identify diverse and subtly-differentiated morphologies. Standard semi-quantitative scoring approaches, however, are coarse-grained and lack precise neuroanatomic localization. We report a proof-of-concept deep learning pipeline that identifies specific neuropathologies—amyloid plaques and cerebral amyloid angiopathy—in immunohistochemically-stained archival slides. Using automated segmentation of stained objects and a cloud-based interface, we annotate > 70,000 plaque candidates from 43 whole slide images (WSIs) to train and evaluate convolutional neural networks. Networks achieve strong plaque classification on a 10-WSI hold-out set (0.993 and 0.743 areas under the receiver operating characteristic and precision recall curve, respectively). Prediction confidence maps visualize morphology distributions at high resolution. Resulting network-derived amyloid beta (Aβ)-burden scores correlate well with established semi-quantitative scores on a 30-WSI blinded hold-out. Finally, saliency mapping demonstrates that networks learn patterns agreeing with accepted pathologic features. This scalable means to augment a neuropathologist’s ability suggests a route to neuropathologic deep phenotyping. Nature Publishing Group UK 2019-05-15 /pmc/articles/PMC6520374/ /pubmed/31092819 http://dx.doi.org/10.1038/s41467-019-10212-1 Text en © The Author(s) 2019 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Tang, Ziqi Chuang, Kangway V. DeCarli, Charles Jin, Lee-Way Beckett, Laurel Keiser, Michael J. Dugger, Brittany N. Interpretable classification of Alzheimer’s disease pathologies with a convolutional neural network pipeline |
title | Interpretable classification of Alzheimer’s disease pathologies with a convolutional neural network pipeline |
title_full | Interpretable classification of Alzheimer’s disease pathologies with a convolutional neural network pipeline |
title_fullStr | Interpretable classification of Alzheimer’s disease pathologies with a convolutional neural network pipeline |
title_full_unstemmed | Interpretable classification of Alzheimer’s disease pathologies with a convolutional neural network pipeline |
title_short | Interpretable classification of Alzheimer’s disease pathologies with a convolutional neural network pipeline |
title_sort | interpretable classification of alzheimer’s disease pathologies with a convolutional neural network pipeline |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6520374/ https://www.ncbi.nlm.nih.gov/pubmed/31092819 http://dx.doi.org/10.1038/s41467-019-10212-1 |
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