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Automated whole slide image analysis for a translational quantification of liver fibrosis

Current literature highlights the need for precise histological quantitative assessment of fibrosis which cannot be achieved by conventional scoring systems, inherent to their discontinuous values and reader-dependent variability. Here we used an automated image analysis software to measure fibrosis...

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Autores principales: Serdjebi, Cindy, Bertotti, Karine, Huang, Pinzhu, Wei, Guangyan, Skelton-Badlani, Disha, Leclercq, Isabelle A., Barbes, Damien, Lepoivre, Bastien, Popov, Yury V., Julé, Yvon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9636208/
https://www.ncbi.nlm.nih.gov/pubmed/36333365
http://dx.doi.org/10.1038/s41598-022-22902-w
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author Serdjebi, Cindy
Bertotti, Karine
Huang, Pinzhu
Wei, Guangyan
Skelton-Badlani, Disha
Leclercq, Isabelle A.
Barbes, Damien
Lepoivre, Bastien
Popov, Yury V.
Julé, Yvon
author_facet Serdjebi, Cindy
Bertotti, Karine
Huang, Pinzhu
Wei, Guangyan
Skelton-Badlani, Disha
Leclercq, Isabelle A.
Barbes, Damien
Lepoivre, Bastien
Popov, Yury V.
Julé, Yvon
author_sort Serdjebi, Cindy
collection PubMed
description Current literature highlights the need for precise histological quantitative assessment of fibrosis which cannot be achieved by conventional scoring systems, inherent to their discontinuous values and reader-dependent variability. Here we used an automated image analysis software to measure fibrosis deposition in two relevant preclinical models of liver fibrosis, and established correlation with other quantitative fibrosis descriptors. Longitudinal quantification of liver fibrosis was carried out during progression of post-necrotic (CCl(4)-induced) and metabolic (HF-CDAA feeding) models of chronic liver disease in mice. Whole slide images of picrosirius red-stained liver sections were analyzed using a fully automated, unsupervised software. Fibrosis was characterized by a significant increase of collagen proportionate area (CPA) at weeks 3 (CCl(4)) and 8 (HF-CDAA) with a progressive increase up to week 18 and 24, respectively. CPA was compared to collagen content assessed biochemically by hydroxyproline assay (HYP) and by standard histological staging systems. CPA showed a high correlation with HYP content for CCl(4) (r = 0.8268) and HF-CDAA (r = 0.6799) models. High correlations were also found with Ishak score or its modified version (r = 0.9705) for CCl(4) and HF-CDAA (r = 0.9062) as well as with NASH CRN for HF-CDAA (r = 0.7937). Such correlations support the use of automated digital analysis as a reliable tool to evaluate the dynamics of liver fibrosis and efficacy of antifibrotic drug candidates in preclinical models.
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spelling pubmed-96362082022-11-06 Automated whole slide image analysis for a translational quantification of liver fibrosis Serdjebi, Cindy Bertotti, Karine Huang, Pinzhu Wei, Guangyan Skelton-Badlani, Disha Leclercq, Isabelle A. Barbes, Damien Lepoivre, Bastien Popov, Yury V. Julé, Yvon Sci Rep Article Current literature highlights the need for precise histological quantitative assessment of fibrosis which cannot be achieved by conventional scoring systems, inherent to their discontinuous values and reader-dependent variability. Here we used an automated image analysis software to measure fibrosis deposition in two relevant preclinical models of liver fibrosis, and established correlation with other quantitative fibrosis descriptors. Longitudinal quantification of liver fibrosis was carried out during progression of post-necrotic (CCl(4)-induced) and metabolic (HF-CDAA feeding) models of chronic liver disease in mice. Whole slide images of picrosirius red-stained liver sections were analyzed using a fully automated, unsupervised software. Fibrosis was characterized by a significant increase of collagen proportionate area (CPA) at weeks 3 (CCl(4)) and 8 (HF-CDAA) with a progressive increase up to week 18 and 24, respectively. CPA was compared to collagen content assessed biochemically by hydroxyproline assay (HYP) and by standard histological staging systems. CPA showed a high correlation with HYP content for CCl(4) (r = 0.8268) and HF-CDAA (r = 0.6799) models. High correlations were also found with Ishak score or its modified version (r = 0.9705) for CCl(4) and HF-CDAA (r = 0.9062) as well as with NASH CRN for HF-CDAA (r = 0.7937). Such correlations support the use of automated digital analysis as a reliable tool to evaluate the dynamics of liver fibrosis and efficacy of antifibrotic drug candidates in preclinical models. Nature Publishing Group UK 2022-11-04 /pmc/articles/PMC9636208/ /pubmed/36333365 http://dx.doi.org/10.1038/s41598-022-22902-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Serdjebi, Cindy
Bertotti, Karine
Huang, Pinzhu
Wei, Guangyan
Skelton-Badlani, Disha
Leclercq, Isabelle A.
Barbes, Damien
Lepoivre, Bastien
Popov, Yury V.
Julé, Yvon
Automated whole slide image analysis for a translational quantification of liver fibrosis
title Automated whole slide image analysis for a translational quantification of liver fibrosis
title_full Automated whole slide image analysis for a translational quantification of liver fibrosis
title_fullStr Automated whole slide image analysis for a translational quantification of liver fibrosis
title_full_unstemmed Automated whole slide image analysis for a translational quantification of liver fibrosis
title_short Automated whole slide image analysis for a translational quantification of liver fibrosis
title_sort automated whole slide image analysis for a translational quantification of liver fibrosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9636208/
https://www.ncbi.nlm.nih.gov/pubmed/36333365
http://dx.doi.org/10.1038/s41598-022-22902-w
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