Cargando…
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...
Autores principales: | , , , , , , , , , |
---|---|
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 |
_version_ | 1784824889280036864 |
---|---|
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. |
format | Online Article Text |
id | pubmed-9636208 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT serdjebicindy automatedwholeslideimageanalysisforatranslationalquantificationofliverfibrosis AT bertottikarine automatedwholeslideimageanalysisforatranslationalquantificationofliverfibrosis AT huangpinzhu automatedwholeslideimageanalysisforatranslationalquantificationofliverfibrosis AT weiguangyan automatedwholeslideimageanalysisforatranslationalquantificationofliverfibrosis AT skeltonbadlanidisha automatedwholeslideimageanalysisforatranslationalquantificationofliverfibrosis AT leclercqisabellea automatedwholeslideimageanalysisforatranslationalquantificationofliverfibrosis AT barbesdamien automatedwholeslideimageanalysisforatranslationalquantificationofliverfibrosis AT lepoivrebastien automatedwholeslideimageanalysisforatranslationalquantificationofliverfibrosis AT popovyuryv automatedwholeslideimageanalysisforatranslationalquantificationofliverfibrosis AT juleyvon automatedwholeslideimageanalysisforatranslationalquantificationofliverfibrosis |