Related Experiment Video
Updated: Jan 7, 2026

Author Spotlight: Establishing MASLD Cell Models for Investigating Disease Mechanisms and the Lipid-Lowering Effects of Koumiss
Published on: July 19, 2024
Correlation of Plasma and Liver Tissue Proteomics for Plasma Biomarkers in Metabolic Dysfunction-Associated Steatotic
Achuthan Sourianarayanane1, Ju-Seog Lee2, Honsoul Kim3
1Division of Gastroenterology and Hepatology, Medical College of Wisconsin, Milwaukee, Wisconsin 53226, United States.
Abstract:
Diagnosing metabolic dysfunction-associated steatohepatitis (MASH) within the spectrum of metabolic dysfunction-associated steatotic liver disease (MASLD) remains challenging. This study evaluates the relationship between plasma proteins and their liver tissue counterparts to assess their potential as diagnostic biomarkers for MASH. An untargeted proteomic analysis was performed on paired liver tissue and plasma samples obtained during biopsies from 7 controls and 64 MASLD patients. Plasma proteins that showed significant correlations with their liver counterparts and exhibited consistent gradients across progressive MASLD stages were evaluated as biomarkers. The study found that liver tissue proteomics showed a strong correlation with MASLD histological severity. Of 356 plasma proteins, 30 showed significant positive correlations (r > 0.5, p < 0.01) with their liver tissue counterparts. Eight proteins exhibited consistent changes across disease stages and distinguished MASH from non-MASH with an area under the receiver operating curve (AUROC) of 0.786 and advanced fibrosis from nonfibrosis cases with an AUROC of 0.874. In conclusion, a limited subset of plasma proteins reflects liver proteomic changes and may serve as biomarkers for distinguishing MASH and fibrosis stages within MASLD.
Related Concept Videos
Effect of Hepatic Disease on Pharmacokinetics: Pathophysiologic Assessment and Liver Function Test
Effect of Hepatic Disease on Pharmacokinetics: Drug Dosing and Hepatic Blood Flow
Liver Physiology
Metabolic Regulation:
The liver is the central organ involved in regulating blood composition. It stabilizes blood glucose levels, maintaining them within the range of 70–110 mg/dL. When these levels drop, the liver breaks down glycogen reserves and releases glucose into the bloodstream. It can...

