Back to Search Start Over

Quantitative digital pathology enables automated and quantitative assessment of inflammatory activity in patients with autoimmune hepatitis.

Authors :
Socha P
Shumbayawonda E
Roy A
Langford C
Aljabar P
Wozniak M
Chełstowska S
Jurkiewicz E
Banerjee R
Fleming K
Pronicki M
Janowski K
Grajkowska W
Source :
Journal of pathology informatics [J Pathol Inform] 2024 Mar 12; Vol. 15, pp. 100372. Date of Electronic Publication: 2024 Mar 12 (Print Publication: 2024).
Publication Year :
2024

Abstract

Background: Chronic liver disease diagnoses depend on liver biopsy histopathological assessment. However, due to the limitations associated with biopsy, there is growing interest in the use of quantitative digital pathology to support pathologists. We evaluated the performance of computational algorithms in the assessment of hepatic inflammation in an autoimmune hepatitis in which inflammation is a major component.<br />Methods: Whole-slide digital image analysis was used to quantitatively characterize the area of tissue covered by inflammation [Inflammation Density (ID)] and number of inflammatory foci per unit area [Focal Density (FD)] on tissue obtained from 50 patients with autoimmune hepatitis undergoing routine liver biopsy. Correlations between digital pathology outputs and traditional categorical histology scores, biochemical, and imaging markers were assessed. The ability of ID and FD to stratify between low-moderate (both portal and lobular inflammation ≤1) and moderate-severe disease activity was estimated using the area under the receiver operating characteristic curve (AUC).<br />Results: ID and FD scores increased significantly and linearly with both portal and lobular inflammation grading. Both ID and FD correlated moderately-to-strongly and significantly with histology (portal and lobular inflammation; 0.36≤R≤0.69) and biochemical markers (ALT, AST, GGT, IgG, and gamma globulins; 0.43≤R≤0.57). ID (AUC: 0.85) and FD (AUC: 0.79) had good performance for stratifying between low-moderate and moderate-severe inflammation.<br />Conclusion: Quantitative assessment of liver biopsy using quantitative digital pathology metrics correlates well with traditional pathology scores and key biochemical markers. Whole-slide quantification of disease can support stratification and identification of patients with more advanced inflammatory disease activity.<br />Competing Interests: The members and employees of The Children's Memorial Health Institute declare no conflict of interest with this study. Perspectum Ltd is a privately funded commercial enterprise that develops medical devices to address unmet clinical needs, including LiverMultiScan. Perspectum is the sponsor of this study. The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Elizabeth Shumbayawonda reports financial support was provided by Perspectum Ltd. Abhishek Roy reports financial support was provided by Perspectum Ltd. Caitlin Langford reports financial support was provided by Perspectum Ltd. Paul Aljabar reports financial support was provided by Perspectum Ltd. Rajarshi Banerjee reports financial support was provided by Perspectum Ltd. Ken Fleming reports financial support was provided by Perspectum Ltd. Elizabeth Shumbayawonda reports a relationship with Perspectum Ltd. that includes: employment and equity or stocks. Abhishek Roy reports a relationship with Perspectum Ltd that includes: employment. Caitlin Langford reports a relationship with Perspectum Ltd that includes: employment. Paul Aljabar reports a relationship with Perspectum Ltd that includes: employment and equity or stocks. Rajarshi Banerjee reports a relationship with Perspectum Ltd that includes: employment and equity or stocks. Ken Fleming reports a relationship with Perspectum Ltd that includes: consulting or advisory.<br /> (© 2024 The Authors.)

Details

Language :
English
ISSN :
2229-5089
Volume :
15
Database :
MEDLINE
Journal :
Journal of pathology informatics
Publication Type :
Academic Journal
Accession number :
38524918
Full Text :
https://doi.org/10.1016/j.jpi.2024.100372