A proteo-transcriptomic map of non-alcoholic fatty liver disease signatures

Nat Metab. 2023 Apr;5(4):572-578. doi: 10.1038/s42255-023-00775-1. Epub 2023 Apr 10.

Abstract

Non-alcoholic fatty liver disease (NAFLD) is a common, progressive liver disease strongly associated with the metabolic syndrome. It is unclear how progression of NAFLD towards cirrhosis translates into systematic changes in circulating proteins. Here, we provide a detailed proteo-transcriptomic map of steatohepatitis and fibrosis during progressive NAFLD. In this multicentre proteomic study, we characterize 4,730 circulating proteins in 306 patients with histologically characterized NAFLD and integrate this with transcriptomic analysis in paired liver tissue. We identify circulating proteomic signatures for active steatohepatitis and advanced fibrosis, and correlate these with hepatic transcriptomics to develop a proteo-transcriptomic signature of 31 markers. Deconvolution of this signature by single-cell RNA sequencing reveals the hepatic cell types likely to contribute to proteomic changes with disease progression. As an exemplar of use as a non-invasive diagnostic, logistic regression establishes a composite model comprising four proteins (ADAMTSL2, AKR1B10, CFHR4 and TREM2), body mass index and type 2 diabetes mellitus status, to identify at-risk steatohepatitis.

Publication types

  • Multicenter Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Body Mass Index
  • Cohort Studies
  • Diabetes Mellitus, Type 2 / complications
  • Disease Progression
  • Fatty Liver / complications
  • Fatty Liver / metabolism
  • Female
  • Gene Expression Profiling*
  • Humans
  • Immunohistochemistry
  • Liver Cirrhosis / complications
  • Liver Cirrhosis / metabolism
  • Logistic Models
  • Male
  • Middle Aged
  • Non-alcoholic Fatty Liver Disease* / complications
  • Non-alcoholic Fatty Liver Disease* / diagnosis
  • Non-alcoholic Fatty Liver Disease* / genetics
  • Non-alcoholic Fatty Liver Disease* / metabolism
  • Proteomics*
  • Registries
  • Single-Cell Gene Expression Analysis

Substances

  • ADAMTSL2 protein, human
  • AKR1B10 protein, human
  • CFHR4 protein, human
  • TREM2 protein, human