Functional polymorphisms of innate immunity receptors are not risk factors for the non-SBP type bacterial infections in cirrhosis

Liver Int. 2018 Jul;38(7):1242-1252. doi: 10.1111/liv.13664. Epub 2018 Jan 17.

Abstract

Background & aims: Pattern recognition receptors (PRRs) have a key role in the innate host defense. Functional polymorphisms of various PRRs have been established to contribute to an increased susceptibility to spontaneous bacterial peritonitis (SBP). Their role in the development of cirrhosis-associated bacterial infections (BI), beyond SBP or progressive disease course related to pathological bacterial translocation (BT) remains unknown.

Methods: Three hundred and forty-nine patients with cirrhosis were genotyped for common NOD2 (R702W, G908R and L1007PfsinsC), TLR2 (-16934T>A), and TLR4 (D299G) variants. Incidence of BIs, decompensating events and liver-related death were assessed in a 5-year follow-up observational study. Pathological BT was assessed based on the presence of antimicrobial antibodies or lipopolysaccharide-binding protein (LBP) level.

Results: In patients with ascites (n = 88) only NOD2 gene variants were associated with an increased cumulative probability of SBP (76.9% ± 19.9%) compared to wild-type (30.9% ± 6.9%, PLogRank = .047). Individual or combined PRR genetic profiles were associated with the risk of non-SBP type BI. Advanced disease stage (HR [95% CI]: 2.11 [1.38-3.25]) and prior history of a BI episode (HR: 2.42 [1.58-3.72]) were the major clinical risk factors of a subsequent BI. The risk of a non-SBP type BI in patients with advanced disease and a prior BI was even higher (HR: 4.74 [2.68-8.39]). The frequency of antimicrobial antibodies and LBP levels did not differ between various PRR genotypes. Correspondingly, PRR genetic profile was not able to predict the long-term disease course.

Conclusions: In cirrhosis, functional polymorphisms of PRRs did not improve the identification of patients with high risk of BI beyond SBP or progressive diseases course.

Keywords: bacterial infection; cirrhosis; compliations; genetic polymorphisms; mortality; pattern recognition receptors.

Publication types

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

MeSH terms

  • Acute-Phase Proteins / analysis
  • Aged
  • Ascites / complications
  • Bacterial Infections / complications*
  • Bacterial Translocation*
  • Carrier Proteins / analysis
  • Female
  • Follow-Up Studies
  • Genetic Predisposition to Disease
  • Humans
  • Hungary
  • Immunity, Innate*
  • Liver Cirrhosis / complications*
  • Liver Cirrhosis / genetics
  • Liver Cirrhosis / mortality
  • Male
  • Membrane Glycoproteins / analysis
  • Middle Aged
  • Multivariate Analysis
  • Nod2 Signaling Adaptor Protein / genetics
  • Peritonitis / diagnosis*
  • Peritonitis / microbiology
  • Polymorphism, Genetic
  • Receptors, Pattern Recognition / genetics*
  • Receptors, Pattern Recognition / immunology
  • Risk Factors
  • Survival Analysis
  • Tertiary Care Centers
  • Toll-Like Receptor 2 / genetics
  • Toll-Like Receptor 4 / genetics

Substances

  • Acute-Phase Proteins
  • Carrier Proteins
  • Membrane Glycoproteins
  • NOD2 protein, human
  • Nod2 Signaling Adaptor Protein
  • Receptors, Pattern Recognition
  • TLR2 protein, human
  • TLR4 protein, human
  • Toll-Like Receptor 2
  • Toll-Like Receptor 4
  • lipopolysaccharide-binding protein