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Deep learning quantification of percent steatosis in donor liver biopsy frozen sections
BACKGROUND: Pathologist evaluation of donor liver biopsies provides information for accepting or discarding potential donor livers. Due to the urgent nature of the decision process, this is regularly performed using frozen sectioning at the time of biopsy. The percent steatosis in a donor liver biop...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7522765/ https://www.ncbi.nlm.nih.gov/pubmed/32980688 http://dx.doi.org/10.1016/j.ebiom.2020.103029 |
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author | Sun, Lulu Marsh, Jon N. Matlock, Matthew K. Chen, Ling Gaut, Joseph P. Brunt, Elizabeth M. Swamidass, S. Joshua Liu, Ta-Chiang |
author_facet | Sun, Lulu Marsh, Jon N. Matlock, Matthew K. Chen, Ling Gaut, Joseph P. Brunt, Elizabeth M. Swamidass, S. Joshua Liu, Ta-Chiang |
author_sort | Sun, Lulu |
collection | PubMed |
description | BACKGROUND: Pathologist evaluation of donor liver biopsies provides information for accepting or discarding potential donor livers. Due to the urgent nature of the decision process, this is regularly performed using frozen sectioning at the time of biopsy. The percent steatosis in a donor liver biopsy correlates with transplant outcome, however there is significant inter- and intra-observer variability in quantifying steatosis, compounded by frozen section artifact. We hypothesized that a deep learning model could identify and quantify steatosis in donor liver biopsies. METHODS: We developed a deep learning convolutional neural network that generates a steatosis probability map from an input whole slide image (WSI) of a hematoxylin and eosin-stained frozen section, and subsequently calculates the percent steatosis. Ninety-six WSI of frozen donor liver sections from our transplant pathology service were annotated for steatosis and used to train (n = 30 WSI) and test (n = 66 WSI) the deep learning model. FINDINGS: The model had good correlation and agreement with the annotation in both the training set (r of 0.88, intraclass correlation coefficient [ICC] of 0.88) and novel input test sets (r = 0.85 and ICC=0.85). These measurements were superior to the estimates of the on-service pathologist at the time of initial evaluation (r = 0.52 and ICC=0.52 for the training set, and r = 0.74 and ICC=0.72 for the test set). INTERPRETATION: Use of this deep learning algorithm could be incorporated into routine pathology workflows for fast, accurate, and reproducible donor liver evaluation. FUNDING: Mid-America Transplant Society |
format | Online Article Text |
id | pubmed-7522765 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-75227652020-10-02 Deep learning quantification of percent steatosis in donor liver biopsy frozen sections Sun, Lulu Marsh, Jon N. Matlock, Matthew K. Chen, Ling Gaut, Joseph P. Brunt, Elizabeth M. Swamidass, S. Joshua Liu, Ta-Chiang EBioMedicine Research Paper BACKGROUND: Pathologist evaluation of donor liver biopsies provides information for accepting or discarding potential donor livers. Due to the urgent nature of the decision process, this is regularly performed using frozen sectioning at the time of biopsy. The percent steatosis in a donor liver biopsy correlates with transplant outcome, however there is significant inter- and intra-observer variability in quantifying steatosis, compounded by frozen section artifact. We hypothesized that a deep learning model could identify and quantify steatosis in donor liver biopsies. METHODS: We developed a deep learning convolutional neural network that generates a steatosis probability map from an input whole slide image (WSI) of a hematoxylin and eosin-stained frozen section, and subsequently calculates the percent steatosis. Ninety-six WSI of frozen donor liver sections from our transplant pathology service were annotated for steatosis and used to train (n = 30 WSI) and test (n = 66 WSI) the deep learning model. FINDINGS: The model had good correlation and agreement with the annotation in both the training set (r of 0.88, intraclass correlation coefficient [ICC] of 0.88) and novel input test sets (r = 0.85 and ICC=0.85). These measurements were superior to the estimates of the on-service pathologist at the time of initial evaluation (r = 0.52 and ICC=0.52 for the training set, and r = 0.74 and ICC=0.72 for the test set). INTERPRETATION: Use of this deep learning algorithm could be incorporated into routine pathology workflows for fast, accurate, and reproducible donor liver evaluation. FUNDING: Mid-America Transplant Society Elsevier 2020-09-24 /pmc/articles/PMC7522765/ /pubmed/32980688 http://dx.doi.org/10.1016/j.ebiom.2020.103029 Text en © 2020 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Paper Sun, Lulu Marsh, Jon N. Matlock, Matthew K. Chen, Ling Gaut, Joseph P. Brunt, Elizabeth M. Swamidass, S. Joshua Liu, Ta-Chiang Deep learning quantification of percent steatosis in donor liver biopsy frozen sections |
title | Deep learning quantification of percent steatosis in donor liver biopsy frozen sections |
title_full | Deep learning quantification of percent steatosis in donor liver biopsy frozen sections |
title_fullStr | Deep learning quantification of percent steatosis in donor liver biopsy frozen sections |
title_full_unstemmed | Deep learning quantification of percent steatosis in donor liver biopsy frozen sections |
title_short | Deep learning quantification of percent steatosis in donor liver biopsy frozen sections |
title_sort | deep learning quantification of percent steatosis in donor liver biopsy frozen sections |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7522765/ https://www.ncbi.nlm.nih.gov/pubmed/32980688 http://dx.doi.org/10.1016/j.ebiom.2020.103029 |
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