Tumor necrosis factor-α and interleukin-1β gene polymorphisms and risk of brain abscess in North Indian population

Cytokine. 2015 Sep;75(1):159-64. doi: 10.1016/j.cyto.2015.07.009. Epub 2015 Jul 14.

Abstract

Objective: Brain abscess develops in response to a parenchymal infection with pyogenic bacteria. Tumor necrosis factor-α (TNF-α) and interleukin-1β (IL-1β) are the most crucial pro-inflammatory cytokines with both beneficial and destructive properties for the central nervous system. The present study evaluated the association of specific alleles/genotypes of TNF-α and IL-1β with brain abscess.

Material and methods: A total of 90 brain abscess patients and 100 healthy controls were included in the study. Predisposing factors were identified in 56 (62.2%) patients with brain abscess. TNF-α (-308 G>A) and IL-1β (-511 C<T) genotypes were detected by PCR-RFLP. Levels of TNF-α and IL-1β were determined in patients' sera and in pus samples by ELISA and correlated with different genotypes.

Results: TNF-α genotypes AA and GA (p<0.001 for AA and p=0.001 for GA), and IL-1β genotypes C/C and C/T (p<0.001 for C/C and p=0.049 for C/T) were significantly associated with brain abscess. Homozygous AA genotype of TNF-α had significant association with brain abscess patients having identified predisposing factors (p=0.026). Patients with heterozygous or homozygous A allele in TNF-α (-308 G>A) and C allele in IL-1β (-511 C<T) had significantly higher levels of TNF-α and IL-1β.

Conclusion: TNF-α (-308 G>A) and IL-1β (-511 C<T) polymorphisms that lead to increased production of TNF-α and IL-1β appear to be risk for development of brain abscess in North Indian population.

Keywords: Brain abscess; IL-1β; Polymorphisms; Serum level; TNF-α.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Alleles
  • Brain / metabolism
  • Brain Abscess / ethnology*
  • Brain Abscess / genetics*
  • Case-Control Studies
  • Child
  • Cytokines / genetics
  • Enzyme-Linked Immunosorbent Assay
  • Female
  • Genetic Predisposition to Disease
  • Genotype
  • Heterozygote
  • Homozygote
  • Humans
  • India
  • Interleukin-1beta / genetics*
  • Male
  • Middle Aged
  • Polymerase Chain Reaction
  • Polymorphism, Genetic*
  • Polymorphism, Restriction Fragment Length
  • Risk Factors
  • Tumor Necrosis Factor-alpha / genetics*
  • Young Adult

Substances

  • Cytokines
  • IL1B protein, human
  • Interleukin-1beta
  • Tumor Necrosis Factor-alpha