Plasma Cytokeratin-18 Fragment Level Reflects the Metabolic Phenotype in Obesity

Biomolecules. 2023 Apr 14;13(4):675. doi: 10.3390/biom13040675.

Abstract

There is growing interest in the non-invasive identification and monitoring of the outcome of liver damage in obese patients. Plasma cytokeratin-18 (CK-18) fragment levels correlate with the magnitude of hepatocyte apoptosis and have recently been proposed to independently predict the presence of non-alcoholic steatohepatitis (NASH). The aim of the study was to analyze the associations of CK-18 with obesity and related complications: insulin resistance, impaired lipid metabolism and the secretion of hepatokines, adipokines and pro-inflammatory cytokines. The study involved 151 overweight and obese patients (BMI 25-40), without diabetes, dyslipidemia or apparent liver disease. Liver function was assessed based on alanine aminotransferase (ALT), gamma-glutamyl transferase (GGT) and the fatty liver index (FLI). CK-18 M30 plasma levels, FGF-21, FGF-19 and cytokines were determined by ELISA. CK-18 values >150 U/l were accompanied by high ALT, GGT and FLI, insulin resistance, postprandial hypertriglyceridemia, elevated FGF-21 and MCP-1 and decreased adiponectin. ALT activity was the strongest independent factor influencing high CK-18 plasma levels, even after an adjustment for age, sex and BMI [β coefficient (95%CI): 0.40 (0.19-0.61)]. In conclusion, the applied CK-18 cut-off point at 150 U/l allows to distinguish between two metabolic phenotypes in obesity.

Keywords: CK-18; FGF-21; cytokeratin-18; fatty liver; obesity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biomarkers / metabolism
  • Cytokines / metabolism
  • Humans
  • Insulin Resistance*
  • Keratin-18
  • Liver / metabolism
  • Non-alcoholic Fatty Liver Disease* / metabolism
  • Obesity / metabolism
  • Phenotype
  • gamma-Glutamyltransferase

Substances

  • Keratin-18
  • Biomarkers
  • gamma-Glutamyltransferase
  • Cytokines

Grants and funding

This research was funded by the European Commission through its Seventh Framework Programme, grant agreement number 244995 (to A.D.K.), and by the Ministry Of Science and Higher Education (PL) grants: number N/41/DBS/000048 (to J.G.) and number K/ZDS/007158 (to A.Z.)