Biomarkers of hepatocellular synthesis in patients with decompensated cirrhosis

• DOI: 10.1007/s12072-022-10473-x
• Publication Date: 2023-01-18T13:03:10Z
• Authors: Berivan Gurbuz; Nurdan Guldiken; Philipp Reuken; Lei Fu; Katharina Remih; Christian Preisinger; Radan Brůha; Martin Leníček; Jaromír Petrtýl; Johanna Reissing; Mahmoud Aly; Malin Fromme; Biaohuan Zhou; Isabel Karkossa; Kristin Schubert; Martin von Bergen; Andreas Stallmach; Tony Bruns; Pavel Strnad
• Keywords: Liver Cirrhosis; Proteomics; Carcinoma, Hepatocellular; Liver Cirrhosis and Associated Complications; Epidemiology; 610; Transthyretin; Gene; Biochemistry; Epidemiology and Management of NAFLD; 03 medical and health sciences; Health Sciences; Humans; Internal medicine; Biology; info:eu-repo/classification/ddc/610; 0303 health sciences; Apolipoprotein A-I; Hepatology; Liver Neoplasms; Gastroenterology; Blood Proteins; Prognosis; Fibrosis; 3. Good health; Cirrhosis; Hepatitis C Infection and Treatment; Medicine; Original Article; Biomarkers

Abstract Background and aim Since hepatocytes produce majority of serum proteins, patients with cirrhosis display substantial alterations in the serum proteome. The aim of the current study was to characterize these changes and to study the prognostic utility of hepatocellular proteins available in routine clinical testing.

Methods Sera from 29 healthy controls and 43 patients with cirrhosis were subjected to untargeted proteomic analysis. Unsupervised hierarchical clustering was performed with Perseus software and R. Ingenuity pathway analysis (IPA) suggested upstream regulators that were validated in liver tissues. The behavior and prognostic usefulness of selected biomarkers was investigated in 61 controls and 285 subjects with decompensated cirrhosis.

Results Proteomics uncovered 65 and 16 hepatocellular serum proteins that are significantly downregulated or upregulated in patients with cirrhosis vs. controls. Hierarchical clustering revealed two main clusters and six sub-clusters. IPA identified HNF4α and IL-6 as the two major upstream regulators that were confirmed by hepatic gene expression analyses. Among pseudocholinesterase, transferrin, transthyretin, albumin, and apolipoprotein AI (Apo-AI), Apo-AI was the best predictor of 90-days transplant-free survival (AUROC 0.678; p = 0.0001) and remained an independent predictor in multivariable Cox independently of the presence of acute-on-chronic liver failure.

Conclusion Our study reveals cirrhosis-associated changes in hepatocellular serum proteins and underlying transcription factors. Serum apolipoprotein AI may constitute a useful prognostic adjunct in patients with decompensated cirrhosis.

Graphical abstract