Association between endotoxemia and histological features of nonalcoholic fatty liver disease

World J Gastroenterol. 2017 Jan 28;23(4):712-722. doi: 10.3748/wjg.v23.i4.712.

Abstract

Aim: To assess whether surrogate biomarkers of endotoxemia were correlated with the histological features of nonalcoholic fatty liver disease (NAFLD).

Methods: One hundred twenty-six NAFLD patients who had undergone percutaneous liver biopsy were enrolled. Serum lipopolysaccharide (LPS)-binding protein (LBP) and anti-endotoxin core immunoglobulin G (EndoCab IgG) antibody concentrations at the time of liver biopsy were measured using the enzyme-linked immunosorbent assays to examine for relationships between biomarker levels and histological scores.

Results: Serum LBP concentration was significantly increased in nonalcoholic steatohepatitis (NASH) patients as compared with nonalcoholic fatty liver (NAFL) subjects and was correlated with steatosis (r = 0.38, P < 0.0001) and ballooning scores (r = 0.23, P = 0.01), but not with the severity of lobular inflammation or fibrosis. Multivariate linear regression analysis revealed that LBP was associated with steatosis score and circulating C-reactive protein, aspartate aminotransferase, and fibrinogen levels. Serum EndoCab IgG concentration was comparable between NASH and NAFL patients. No meaningful correlations were detected between EndoCab IgG and histological findings.

Conclusion: LBP/EndoCab IgG were not correlated with lobular inflammation or fibrosis. More accurate LPS biomarkers are required to stringently assess the contribution of endotoxemia to conventional NASH.

Keywords: EndoCab IgG; Endotoxemia; Fibrosis; Lipopolysaccharide-binding protein; Nonalcoholic steatohepatitis; Steatosis.

MeSH terms

  • Acute-Phase Proteins
  • Adult
  • Aged
  • Biomarkers / blood*
  • Biopsy
  • Carrier Proteins / blood
  • Endotoxemia / blood*
  • Endotoxemia / diagnosis
  • Fatty Liver / blood*
  • Fatty Liver / diagnosis
  • Female
  • Fibrosis
  • Humans
  • Immunoglobulin G / blood
  • Inflammation
  • Liver / pathology
  • Male
  • Membrane Glycoproteins / blood
  • Middle Aged
  • Multivariate Analysis
  • Non-alcoholic Fatty Liver Disease / blood*
  • Non-alcoholic Fatty Liver Disease / diagnosis
  • Retrospective Studies

Substances

  • Acute-Phase Proteins
  • Biomarkers
  • Carrier Proteins
  • Immunoglobulin G
  • Membrane Glycoproteins
  • lipopolysaccharide-binding protein