Serum metabolome alterations in patients with early nonalcoholic fatty liver disease

Biosci Rep. 2022 Oct 28;42(10):BSR20220319. doi: 10.1042/BSR20220319.

Abstract

Background: Although metabolomic analysis for patients with nonalcoholic fatty liver disease (NAFLD) was a promising approach to identify novel biomarkers as targets for the diagnosis of NAFLD, the serum metabolomics profile of early-stage NAFLD patients from central China remain unknown.

Objective: The aim of the present study was to explore the metabolic characteristics of patients with early-stage NAFLD based on the ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) technology, to identify differential metabolites and perform functional analysis, and especially, to establish a novel early NAFLD clinical diagnostic tool.

Results: Compared with healthy controls, serum metabolite species increased significantly in early stage NAFLD patients. Expression of 88 metabolites including 1-naphthylmethanol, rosavin, and theophylline were up-regulated in early NAFLD, while 68 metabolites including 2-hydroxyphenylacetic acid and lysophosphatidylcholine (24:1(15Z)) were down-regulated. The early NAFLD classifier achieved a strong diagnostic efficiency in the discovery phases (80.99%) and was successfully verified in the validation phases (75.23%).

Conclusions: These results advance our understanding about the composition and biological functions of serum metabolites of early NAFLD. In addition, serum metabolic markers can serve as an efficient diagnostic tool for the early-stage NAFLD.

Keywords: Diagnostic Markers; Diagnostic Model; Early-stage Nonalcoholic Fatty Liver; Metabolites; Serum Metabolomics.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biomarkers
  • Chromatography, Liquid
  • Humans
  • Lysophosphatidylcholines
  • Metabolome
  • Metabolomics / methods
  • Non-alcoholic Fatty Liver Disease*
  • Tandem Mass Spectrometry
  • Theophylline

Substances

  • Lysophosphatidylcholines
  • Theophylline
  • Biomarkers