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Deep Learning Based Accurate Hepatic Steatosis Quantification for Histological Assessment of Liver Biopsies

Hepatic steatosis droplet quantification with histology biopsies has high clinical significance for risk stratification and management of patients with fatty liver diseases and in the decision to use donor livers for transplantation. However, pathology reviewing processes, when conducted manually, a...

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Autores principales: Roy, Mousumi, Wang, Fusheng, Vo, Hoang, Teng, Dejun, Teodoro, George, Farris, Alton B., Castillo-Leon, Eduardo, Vos, Miriam B., Kong, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7502534/
https://www.ncbi.nlm.nih.gov/pubmed/32661341
http://dx.doi.org/10.1038/s41374-020-0463-y
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author Roy, Mousumi
Wang, Fusheng
Vo, Hoang
Teng, Dejun
Teodoro, George
Farris, Alton B.
Castillo-Leon, Eduardo
Vos, Miriam B.
Kong, Jun
author_facet Roy, Mousumi
Wang, Fusheng
Vo, Hoang
Teng, Dejun
Teodoro, George
Farris, Alton B.
Castillo-Leon, Eduardo
Vos, Miriam B.
Kong, Jun
author_sort Roy, Mousumi
collection PubMed
description Hepatic steatosis droplet quantification with histology biopsies has high clinical significance for risk stratification and management of patients with fatty liver diseases and in the decision to use donor livers for transplantation. However, pathology reviewing processes, when conducted manually, are subject to a high inter- and intra-reader variability, due to the overwhelmingly large number and significantly varying appearance of steatosis instances. Meanwhile, this process is challenging as there is a large number of overlapped steatosis droplets with either missing or weak boundaries. In this study, we propose a deep learning based region-boundary integrated network for precise steatosis quantification with whole slide liver histopathology images. The proposed model consists of two sequential steps: a region extraction and a boundary prediction module for foreground regions and steatosis boundary prediction, followed by an integrated prediction map generation. Missing steatosis boundaries are next recovered from the predicted map and assembled from adjacent image patches to generate results for the whole slide histopathology image. The resulting steatosis measures both at the pixel level and steatosis object level present strong correlation with pathologist annotations, radiology readouts and clinical data. In addition, the segregated steatosis object count is shown as a promising alternative measure to the traditional metrics at the pixel level. These results suggest a high potential of AI assisted technology to enhance liver disease decision support using whole slide images.
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spelling pubmed-75025342021-01-13 Deep Learning Based Accurate Hepatic Steatosis Quantification for Histological Assessment of Liver Biopsies Roy, Mousumi Wang, Fusheng Vo, Hoang Teng, Dejun Teodoro, George Farris, Alton B. Castillo-Leon, Eduardo Vos, Miriam B. Kong, Jun Lab Invest Article Hepatic steatosis droplet quantification with histology biopsies has high clinical significance for risk stratification and management of patients with fatty liver diseases and in the decision to use donor livers for transplantation. However, pathology reviewing processes, when conducted manually, are subject to a high inter- and intra-reader variability, due to the overwhelmingly large number and significantly varying appearance of steatosis instances. Meanwhile, this process is challenging as there is a large number of overlapped steatosis droplets with either missing or weak boundaries. In this study, we propose a deep learning based region-boundary integrated network for precise steatosis quantification with whole slide liver histopathology images. The proposed model consists of two sequential steps: a region extraction and a boundary prediction module for foreground regions and steatosis boundary prediction, followed by an integrated prediction map generation. Missing steatosis boundaries are next recovered from the predicted map and assembled from adjacent image patches to generate results for the whole slide histopathology image. The resulting steatosis measures both at the pixel level and steatosis object level present strong correlation with pathologist annotations, radiology readouts and clinical data. In addition, the segregated steatosis object count is shown as a promising alternative measure to the traditional metrics at the pixel level. These results suggest a high potential of AI assisted technology to enhance liver disease decision support using whole slide images. 2020-07-13 2020-10 /pmc/articles/PMC7502534/ /pubmed/32661341 http://dx.doi.org/10.1038/s41374-020-0463-y Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Roy, Mousumi
Wang, Fusheng
Vo, Hoang
Teng, Dejun
Teodoro, George
Farris, Alton B.
Castillo-Leon, Eduardo
Vos, Miriam B.
Kong, Jun
Deep Learning Based Accurate Hepatic Steatosis Quantification for Histological Assessment of Liver Biopsies
title Deep Learning Based Accurate Hepatic Steatosis Quantification for Histological Assessment of Liver Biopsies
title_full Deep Learning Based Accurate Hepatic Steatosis Quantification for Histological Assessment of Liver Biopsies
title_fullStr Deep Learning Based Accurate Hepatic Steatosis Quantification for Histological Assessment of Liver Biopsies
title_full_unstemmed Deep Learning Based Accurate Hepatic Steatosis Quantification for Histological Assessment of Liver Biopsies
title_short Deep Learning Based Accurate Hepatic Steatosis Quantification for Histological Assessment of Liver Biopsies
title_sort deep learning based accurate hepatic steatosis quantification for histological assessment of liver biopsies
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7502534/
https://www.ncbi.nlm.nih.gov/pubmed/32661341
http://dx.doi.org/10.1038/s41374-020-0463-y
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