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Clinical validation of an AI-based pathology tool for scoring of metabolic dysfunction-associated steatohepatitis

Authors :
Pulaski, Hanna
Harrison, Stephen A.
Mehta, Shraddha S.
Sanyal, Arun J.
Vitali, Marlena C.
Manigat, Laryssa C.
Hou, Hypatia
Madasu Christudoss, Susan P.
Hoffman, Sara M.
Stanford-Moore, Adam
Egger, Robert
Glickman, Jonathan
Resnick, Murray
Patel, Neel
Taylor, Cristin E.
Myers, Robert P.
Chung, Chuhan
Patterson, Scott D.
Sejling, Anne-Sophie
Minnich, Anne
Baxi, Vipul
Subramaniam, G. Mani
Anstee, Quentin M.
Loomba, Rohit
Ratziu, Vlad
Montalto, Michael C.
Anderson, Nick P.
Beck, Andrew H.
Wack, Katy E.
Source :
Nature Medicine; 20240101, Issue: Preprints p1-8, 8p
Publication Year :
2024

Abstract

Metabolic dysfunction-associated steatohepatitis (MASH) is a major cause of liver-related morbidity and mortality, yet treatment options are limited. Manual scoring of liver biopsies, currently the gold standard for clinical trial enrollment and endpoint assessment, suffers from high reader variability. This study represents the most comprehensive multisite analytical and clinical validation of an artificial intelligence (AI)-based pathology system, AI-based measurement of metabolic dysfunction-associated steatohepatitis (AIM-MASH), to assist pathologists in MASH trial histology scoring. AIM-MASH demonstrated high repeatability and reproducibility compared to manual scoring. AIM-MASH-assisted reads by expert MASH pathologists were superior to unassisted reads in accurately assessing inflammation, ballooning, MAS ≥ 4 with ≥1 in each score category and MASH resolution, while maintaining non-inferiority in steatosis and fibrosis assessment. These findings suggest that AIM-MASH could mitigate reader variability, providing a more reliable assessment of therapeutics in MASH clinical trials.

Details

Language :
English
ISSN :
10788956 and 1546170X
Issue :
Preprints
Database :
Supplemental Index
Journal :
Nature Medicine
Publication Type :
Periodical
Accession number :
ejs67900393
Full Text :
https://doi.org/10.1038/s41591-024-03301-2