Association between positivity of serum autoantibodies and liver disease severity in patients with biopsy-proven NAFLD

Nutr Metab Cardiovasc Dis. 2021 Feb 8;31(2):552-560. doi: 10.1016/j.numecd.2020.10.004. Epub 2020 Oct 13.

Abstract

Background and aims: Some previous studies reported serum autoantibody positivity in patients with nonalcoholic fatty liver disease (NAFLD). The clinical significance of these findings remains uncertain. We aimed to investigate the association between the presence of serum autoantibodies and liver disease severity in NAFLD.

Methods and results: A total of 388 consecutive patients with biopsy-proven NAFLD were included in the study. Various serum autoantibodies (including also anti-nuclear antibodies [ANA]) were detected by indirect immunofluorescent or immunoblotting assays. Overall, 84 (21.6%) patients with biopsy-confirmed NAFLD had positivity for at least one of the measured serum autoantibodies. ANA positivity was present in 50 (12.9%) patients, whereas anti-U1RNP or pANCA antibodies were detectable in 9 (2.3%) and 6 (1.5%) patients, respectively. Multivariate logistic regression analysis showed that ANA positivity (adjusted-odds ratio: 4.51, 95%CI: 1.77-11.5; P = 0.002) or positivity of any serum autoantibodies (adjusted-odds ratio: 3.14, 95%CI: 1.30-7.62; P = 0.01) were independently associated with advanced liver fibrosis (stages F3-F4). In serum autoantibody/ANA-positive patients, the proportion of those with advanced fibrosis was also greater among carriers of PNPLA3 rs738409 GG or CG than among those carrying PNPLA3 rs738409 CC genotype.

Conclusions: Serum autoantibody positivity was independently associated with advanced liver fibrosis in patients with biopsy-proven NAFLD. The presence of serum autoantibodies in patients with advanced fibrosis occurred more frequently amongst those carrying PNPLA3 rs738409 GG or CG genotypes.

Keywords: Autoantibodies; Fibrosis; Liver biopsy; NAFLD.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Autoantibodies / blood*
  • Biomarkers / blood
  • Biopsy
  • Cross-Sectional Studies
  • Female
  • Humans
  • Lipase / genetics
  • Liver / pathology*
  • Liver Cirrhosis / blood*
  • Liver Cirrhosis / genetics
  • Liver Cirrhosis / immunology
  • Liver Cirrhosis / pathology
  • Male
  • Membrane Proteins / genetics
  • Middle Aged
  • Non-alcoholic Fatty Liver Disease / blood*
  • Non-alcoholic Fatty Liver Disease / genetics
  • Non-alcoholic Fatty Liver Disease / immunology
  • Non-alcoholic Fatty Liver Disease / pathology
  • Polymorphism, Single Nucleotide
  • Risk Factors
  • Severity of Illness Index

Substances

  • Autoantibodies
  • Biomarkers
  • Membrane Proteins
  • Lipase
  • adiponutrin, human