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Color correction for automatic fibrosis quantification in liver biopsy specimens

CONTEXT: For a precise and objective quantification of liver fibrosis, quantitative evaluations through image analysis have been utilized. However, manual operations are required in most cases for extracting fiber areas because of color variation included in digital pathology images. AIMS: The purpo...

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Autores principales: Murakami, Yuri, Abe, Tokiya, Hashiguchi, Akinori, Yamaguchi, Masahiro, Saito, Akira, Sakamoto, Michiie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3908497/
https://www.ncbi.nlm.nih.gov/pubmed/24524002
http://dx.doi.org/10.4103/2153-3539.124009
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author Murakami, Yuri
Abe, Tokiya
Hashiguchi, Akinori
Yamaguchi, Masahiro
Saito, Akira
Sakamoto, Michiie
author_facet Murakami, Yuri
Abe, Tokiya
Hashiguchi, Akinori
Yamaguchi, Masahiro
Saito, Akira
Sakamoto, Michiie
author_sort Murakami, Yuri
collection PubMed
description CONTEXT: For a precise and objective quantification of liver fibrosis, quantitative evaluations through image analysis have been utilized. However, manual operations are required in most cases for extracting fiber areas because of color variation included in digital pathology images. AIMS: The purpose of this research is to propose a color correction method for whole slide images (WSIs) of Elastica van Gieson (EVG) stained liver biopsy tissue specimens and to realize automated operation of image analysis for fibrosis quantification. MATERIALS AND METHODS: Our experimental dataset consisted of 38 WSIs of liver biopsy specimens collected from 38 chronic viral hepatitis patients from multiple medical facilities, stained with EVG and scanned at ×20 using a Nano Zoomer 2.0 HT (Hamamatsu Photonics K.K., Hamamatsu, Japan). Color correction was performed by modifying the color distribution of a target WSI so as to fit to the reference, where the color distribution was modeled by a set of two triangle pyramids. Using color corrected WSIs; fibrosis quantification was performed based on tissue classification analysis. STATISTICAL ANALYSIS USED: Spearman's rank correlation coefficients were calculated between liver stiffness measured by transient elastography and median area ratio of collagen fibers calculated based on tissue classification results. RESULTS: Statistical analysis results showed a significant correlation r = 0.61-0.68 even when tissue classifiers were trained by using a subset of WSIs, while the correlation coefficients were reduced to r = 0.40-0.50 without color correction. CONCLUSIONS: Fibrosis quantification accompanied with the proposed color correction method could provide an objective evaluation tool for liver fibrosis, which complements semi-quantitative histologic evaluation systems.
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spelling pubmed-39084972014-02-12 Color correction for automatic fibrosis quantification in liver biopsy specimens Murakami, Yuri Abe, Tokiya Hashiguchi, Akinori Yamaguchi, Masahiro Saito, Akira Sakamoto, Michiie J Pathol Inform Original Article CONTEXT: For a precise and objective quantification of liver fibrosis, quantitative evaluations through image analysis have been utilized. However, manual operations are required in most cases for extracting fiber areas because of color variation included in digital pathology images. AIMS: The purpose of this research is to propose a color correction method for whole slide images (WSIs) of Elastica van Gieson (EVG) stained liver biopsy tissue specimens and to realize automated operation of image analysis for fibrosis quantification. MATERIALS AND METHODS: Our experimental dataset consisted of 38 WSIs of liver biopsy specimens collected from 38 chronic viral hepatitis patients from multiple medical facilities, stained with EVG and scanned at ×20 using a Nano Zoomer 2.0 HT (Hamamatsu Photonics K.K., Hamamatsu, Japan). Color correction was performed by modifying the color distribution of a target WSI so as to fit to the reference, where the color distribution was modeled by a set of two triangle pyramids. Using color corrected WSIs; fibrosis quantification was performed based on tissue classification analysis. STATISTICAL ANALYSIS USED: Spearman's rank correlation coefficients were calculated between liver stiffness measured by transient elastography and median area ratio of collagen fibers calculated based on tissue classification results. RESULTS: Statistical analysis results showed a significant correlation r = 0.61-0.68 even when tissue classifiers were trained by using a subset of WSIs, while the correlation coefficients were reduced to r = 0.40-0.50 without color correction. CONCLUSIONS: Fibrosis quantification accompanied with the proposed color correction method could provide an objective evaluation tool for liver fibrosis, which complements semi-quantitative histologic evaluation systems. Medknow Publications & Media Pvt Ltd 2013-12-31 /pmc/articles/PMC3908497/ /pubmed/24524002 http://dx.doi.org/10.4103/2153-3539.124009 Text en Copyright: © 2013 Murakami Y http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Original Article
Murakami, Yuri
Abe, Tokiya
Hashiguchi, Akinori
Yamaguchi, Masahiro
Saito, Akira
Sakamoto, Michiie
Color correction for automatic fibrosis quantification in liver biopsy specimens
title Color correction for automatic fibrosis quantification in liver biopsy specimens
title_full Color correction for automatic fibrosis quantification in liver biopsy specimens
title_fullStr Color correction for automatic fibrosis quantification in liver biopsy specimens
title_full_unstemmed Color correction for automatic fibrosis quantification in liver biopsy specimens
title_short Color correction for automatic fibrosis quantification in liver biopsy specimens
title_sort color correction for automatic fibrosis quantification in liver biopsy specimens
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3908497/
https://www.ncbi.nlm.nih.gov/pubmed/24524002
http://dx.doi.org/10.4103/2153-3539.124009
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