Published online Mar 28, 2026. doi: 10.3748/wjg.v32.i12.113939
Revised: October 24, 2025
Accepted: January 28, 2026
Published online: March 28, 2026
Processing time: 192 Days and 18.5 Hours
Ballooned hepatocytes are a histological hallmark in the diagnosis of metabolic dysfunction-associated steatohepatitis (MASH). Identifying ballooned hepa
To investigate the utility of immunostaining for positive SHH protein expression in ballooned hepatocytes in MASH.
Clinicopathological data from hospitalized patients with metabolic dysfunction-associated steatotic liver (MASL) disease at the Second Hospital of Nanjing from January 2020 to November 2022 were analyzed. The Nonalcoholic Steatohepatitis Clinical Research Network scoring system was used. Post-staining, digitized images were acquired, and area quantification algorithms were used to quantify SHH expression.
A total of 190 MASL disease patients who underwent liver biopsy were enrolled in this study; 58.9% (112/190) had definite MASH, and 41.1% (78/190) had MASL. There were significant differences in body mass index (P < 0.001), diabetes (P < 0.01), metabolic syndrome (P < 0.02), and circulating M65 and M30 (P < 0.001), as well as aspartate aminotransferase (AST), alanine aminotransferase, glucose, uric acid, controlled attenuation parameter (CAP), liver stiffness measurement, and nonalcoholic fatty liver disease fibrosis score (P < 0.05). Serum M30 and M65 levels were almost three times greater in MASH than in MASL patients. Hepatic SHH expression correlated with cir
Hepatic SHH protein expression assisted in the diagnosis of MASH. SHH immunostaining may be useful for classifying and quantifying ballooned hepatocytes by artificial intelligence algorithms.
Core Tip: This is a retrospective cohort study of the characteristics of metabolic dysfunction-associated steatohepatitis, in which we found the suggestive role of sonic hedgehog immunostaining in the diagnosis of metabolic dysfunction-associated steatohepatitis. We also found that histological ballooning hepatocytes and circulating M30 as independent predictors of advanced fibrosis.
