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Liver Tissue Proteins Improve the Accuracy of Plasma Proteins as Biomarkers in Diagnosing Metabolic Dysfunction-Associated Steatohepatitis.

Authors :
Sourianarayanane A
Salemi MR
Phinney BS
McCullough AJ
Source :
Proteomics. Clinical applications [Proteomics Clin Appl] 2024 Nov; Vol. 18 (6), pp. e202300236. Date of Electronic Publication: 2024 Jul 28.
Publication Year :
2024

Abstract

Background: Biomarkers for metabolic dysfunction-associated steatohepatitis (MASH) have been considered based on proteomic and lipidomic data from plasma and liver tissue without clinical benefits. This study evaluated proteomics-based plasma and liver tissue biomarkers collected simultaneously from patients with metabolic dysfunction-associated steatotic liver disease (MASLD).<br />Methods: Liver tissue and plasma samples were collected during liver biopsy to diagnose MASLD. Untargeted proteomics was performed on 64 patients.<br />Results: Twenty plasma proteins were up- or downregulated in patients with MASH compared with those without MASH. The potential biomarkers utilizing the best combinations of these plasma proteins had an area under the receiver operating curve (AUROC) of 0.671 for detecting those with MASH compared with those without it. However, none of the 20 plasma proteins were represented among the significantly regulated liver tissue proteins in patients with MASH. Ten of them displayed a trend and relevance in liver tissue with MASLD progression. These 10 plasma proteins had an AUROC of 0.793 for MASH identification and higher positive and negative predictive values.<br />Conclusion: The plasma and liver protein expressions of patients with MASH were not directly comparable. Plasma protein biomarkers that are also expressed in liver tissue can help improve MASH detection.<br /> (© 2024 Wiley‐VCH GmbH.)

Details

Language :
English
ISSN :
1862-8354
Volume :
18
Issue :
6
Database :
MEDLINE
Journal :
Proteomics. Clinical applications
Publication Type :
Academic Journal
Accession number :
39073724
Full Text :
https://doi.org/10.1002/prca.202300236