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Deep neural network based histological scoring of lung fibrosis and inflammation in the mouse model system

Preclinical studies of novel compounds rely on quantitative readouts from animal models. Frequently employed readouts from histopathological tissue scoring are time consuming, require highly specialized staff and are subject to inherent variability. Recent advances in deep convolutional neural netwo...

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Autores principales: Heinemann, Fabian, Birk, Gerald, Schoenberger, Tanja, Stierstorfer, Birgit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6107205/
https://www.ncbi.nlm.nih.gov/pubmed/30138413
http://dx.doi.org/10.1371/journal.pone.0202708
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author Heinemann, Fabian
Birk, Gerald
Schoenberger, Tanja
Stierstorfer, Birgit
author_facet Heinemann, Fabian
Birk, Gerald
Schoenberger, Tanja
Stierstorfer, Birgit
author_sort Heinemann, Fabian
collection PubMed
description Preclinical studies of novel compounds rely on quantitative readouts from animal models. Frequently employed readouts from histopathological tissue scoring are time consuming, require highly specialized staff and are subject to inherent variability. Recent advances in deep convolutional neural networks (CNN) now allow automating such scoring tasks. Here, we demonstrate this for the case of the Ashcroft fibrosis score and a newly developed inflammation score to characterize fibrotic and inflammatory lung diseases. Sections of lung tissue from mice exhibiting a wide range of fibrotic and inflammatory states were stained with Masson trichrome. Whole slide scans using a 20x objective were acquired and cut into smaller tiles of 512x512 pixels. The tiles were subsequently classified by specialized CNNs, either an “Ashcroft fibrosis CNN” or an “inflammation CNN”. For the Ashcroft fibrosis score the CNN was fine-tuned by using 14000 labelled tiles. For the inflammation score the CNN was trained with 3500 labelled tiles. After training, the Ashcroft fibrosis CNN achieved an accuracy of 79.5% and the inflammation CNN an accuracy of 80.0%. An error analysis revealed that misclassifications are almost exclusively with neighboring scores, which reflects the inherent ambiguity of parts of the data. The variability between two experts was found to be larger than the variability between the CNN classifications and the ground truth. The CNN generated Ashcroft score was in very good agreement with the score of a pathologist (r(2) = 0.92). Our results demonstrate that costly and time consuming scoring tasks can be automated and standardized with deep learning. New scores such as the inflammation score can be easily developed with the approach presented here.
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spelling pubmed-61072052018-08-30 Deep neural network based histological scoring of lung fibrosis and inflammation in the mouse model system Heinemann, Fabian Birk, Gerald Schoenberger, Tanja Stierstorfer, Birgit PLoS One Research Article Preclinical studies of novel compounds rely on quantitative readouts from animal models. Frequently employed readouts from histopathological tissue scoring are time consuming, require highly specialized staff and are subject to inherent variability. Recent advances in deep convolutional neural networks (CNN) now allow automating such scoring tasks. Here, we demonstrate this for the case of the Ashcroft fibrosis score and a newly developed inflammation score to characterize fibrotic and inflammatory lung diseases. Sections of lung tissue from mice exhibiting a wide range of fibrotic and inflammatory states were stained with Masson trichrome. Whole slide scans using a 20x objective were acquired and cut into smaller tiles of 512x512 pixels. The tiles were subsequently classified by specialized CNNs, either an “Ashcroft fibrosis CNN” or an “inflammation CNN”. For the Ashcroft fibrosis score the CNN was fine-tuned by using 14000 labelled tiles. For the inflammation score the CNN was trained with 3500 labelled tiles. After training, the Ashcroft fibrosis CNN achieved an accuracy of 79.5% and the inflammation CNN an accuracy of 80.0%. An error analysis revealed that misclassifications are almost exclusively with neighboring scores, which reflects the inherent ambiguity of parts of the data. The variability between two experts was found to be larger than the variability between the CNN classifications and the ground truth. The CNN generated Ashcroft score was in very good agreement with the score of a pathologist (r(2) = 0.92). Our results demonstrate that costly and time consuming scoring tasks can be automated and standardized with deep learning. New scores such as the inflammation score can be easily developed with the approach presented here. Public Library of Science 2018-08-23 /pmc/articles/PMC6107205/ /pubmed/30138413 http://dx.doi.org/10.1371/journal.pone.0202708 Text en © 2018 Heinemann et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Heinemann, Fabian
Birk, Gerald
Schoenberger, Tanja
Stierstorfer, Birgit
Deep neural network based histological scoring of lung fibrosis and inflammation in the mouse model system
title Deep neural network based histological scoring of lung fibrosis and inflammation in the mouse model system
title_full Deep neural network based histological scoring of lung fibrosis and inflammation in the mouse model system
title_fullStr Deep neural network based histological scoring of lung fibrosis and inflammation in the mouse model system
title_full_unstemmed Deep neural network based histological scoring of lung fibrosis and inflammation in the mouse model system
title_short Deep neural network based histological scoring of lung fibrosis and inflammation in the mouse model system
title_sort deep neural network based histological scoring of lung fibrosis and inflammation in the mouse model system
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6107205/
https://www.ncbi.nlm.nih.gov/pubmed/30138413
http://dx.doi.org/10.1371/journal.pone.0202708
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