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

被引:4
|
作者
Serdjebi, Cindy [1 ]
Bertotti, Karine [1 ]
Huang, Pinzhu [2 ]
Wei, Guangyan [2 ,3 ]
Skelton-Badlani, Disha [2 ]
Leclercq, Isabelle A. [4 ]
Barbes, Damien [1 ]
Lepoivre, Bastien [1 ]
Popov, Yury, V [2 ]
Jule, Yvon [1 ]
机构
[1] Biocellvia, 10 Rue Grignan, F-13001 Marseille, France
[2] Harvard Med Sch, Beth Israel Deaconess Med Ctr, Div Gastroenterol Hepatol & Nutr, 330 Brookline Ave, Boston, MA 02215 USA
[3] Sun Yat Sen Univ, Affiliated Hosp 1, Dept Radiat Oncol, 58 Zhongshan 2nd Rd, Guangzhou, Guangdong, Peoples R China
[4] Univ Catholique Louvain UCLouvain, Lab HepatoGastroenterol, Inst Rech Expt & Clin, Ave Emmanuel Mounier 52, B-1200 Brussels, Belgium
关键词
COLLAGEN; PROGRESSION; ACTIVATION; DISEASE; MODELS;
D O I
10.1038/s41598-022-22902-w
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
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页数:9
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