Your browser doesn't support javascript.
loading
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.
Afiliación
  • Serdjebi C; Biocellvia, 10 Rue Grignan, 13001, Marseille, France. cindy.serdjebi@biocellvia.com.
  • Bertotti K; Biocellvia, 10 Rue Grignan, 13001, Marseille, France.
  • Huang P; Division of Gastroenterology, Hepatology and Nutrition, Beth Israel Deaconess Medical Center, Harvard Medical School, 330 Brookline Ave, Boston, MA, 02215, USA.
  • Wei G; Division of Gastroenterology, Hepatology and Nutrition, Beth Israel Deaconess Medical Center, Harvard Medical School, 330 Brookline Ave, Boston, MA, 02215, USA.
  • Skelton-Badlani D; Department of Radiation Oncology, The First Affiliated Hospital of Sun Yat-Sen University, 58 Zhongshan 2Nd Rd, Yuexiu District, Guangzhou, Guangdong Province, China.
  • Leclercq IA; Division of Gastroenterology, Hepatology and Nutrition, Beth Israel Deaconess Medical Center, Harvard Medical School, 330 Brookline Ave, Boston, MA, 02215, USA.
  • Barbes D; Laboratory of Hepato-Gastroenterology, Institut de Recherche Expérimentale Et Clinique, Université Catholique de Louvain (UCLouvain), Avenue Emmanuel Mounier 52, 1200, Brussels, Belgium.
  • Lepoivre B; Biocellvia, 10 Rue Grignan, 13001, Marseille, France.
  • Popov YV; Biocellvia, 10 Rue Grignan, 13001, Marseille, France.
  • Julé Y; Division of Gastroenterology, Hepatology and Nutrition, Beth Israel Deaconess Medical Center, Harvard Medical School, 330 Brookline Ave, Boston, MA, 02215, USA.
Sci Rep ; 12(1): 17935, 2022 11 04.
Article en En | MEDLINE | ID: mdl-36333365
ABSTRACT
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 (CCl4-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 (CCl4) 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 CCl4 (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 CCl4 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.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Hígado / Cirrosis Hepática Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Sci Rep Año: 2022 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Hígado / Cirrosis Hepática Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Sci Rep Año: 2022 Tipo del documento: Article País de afiliación: Francia