Basic Mechanisms of MASH Progression

This session explores emerging mechanisms that govern the development and progression of metabolic dysfunction–associated steatotic liver disease and steatohepatitis. Presentations will examine how hepatocyte metabolic programs, macrophage efferocytosis, bile acid signaling, natural killer cell dysfunction, aging-related ferroptosis, and fibrosis-associated cellular states contribute to liver injury and fibrogenesis. The session will also highlight translational insights from preclinical models, including the potential of FGF21-based therapy to promote fibrosis regression and prevent hepatocellular carcinoma.

Advancing Risk Stratification in MASLD and MASH: Biomarkers, Machine Learning, and Noninvasive Tools

This session will highlight emerging approaches to identifying patients with steatotic liver disease who are at greatest risk for advanced liver disease and adverse outcomes. Presentations will explore the role of lipid biomarkers, body phenotype, alcohol exposure assessment, noninvasive diagnostic criteria, and adaptive machine-learning strategies. Together, these studies underscore the evolving role of precision risk stratification in MASLD, MASH cirrhosis, and clinical trial prescreening.

Emerging Mechanisms and Therapeutic Targets in Liver Fibrogenesis

This session focuses on emerging mechanisms of liver fibrogenesis and novel antifibrotic therapeutic strategies. Topics include hepatic stellate cell activation, extracellular matrix remodeling, metabolic and epigenetic regulation of fibrosis, and innovative cell- and RNA-based therapies. Through mechanistic and translational studies, speakers will highlight new opportunities to prevent, halt, and reverse liver fibrosis.
 

Clinical Plenary #2

Alcohol is a major contributor to liver disease, yet diagnostic plans and treatment approaches are not standard around the globe.  This SOA lecture is aimed to explore a multidisciplinary appraoch to evaluation and treatment.

Clinical Plenary #1

Very recent experiences of gene therapy for non-liver disorders has, in rare cases, led to several serious hepatic toxicities including liver failure.  Understanding hepatic pathophysiology, monitoring and therapeutic approaches in the modern era of gene therapy is crucial.

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