Lack of association between an interleukin 1 beta (IL-1beta) gene variation and refractory temporal lobe epilepsy

Epilepsia. 2001 Jun;42(6):782-4. doi: 10.1046/j.1528-1157.2001.42900.x.

Abstract

Purpose: We attempted to confirm recent findings of Kanemoto et al. that demonstrated a positive association (p < 0.017) between a polymorphism in the promoter region of the interleukin 1-beta (IL-1beta) gene and the clinical phenotype of temporal lobe epilepsy with hippocampal sclerosis (TLE+HS).

Methods: We determined the frequency of this polymorphism in a group of 61 TLE+HS patients of European ancestry and compared it with that found in 119 ethnically matched control subjects.

Results: Analysis of genotype and allele frequencies showed no statistically significant difference in the distribution of the polymorphism between the two groups (p = 0.10).

Conclusions: These data suggest that this IL-1beta promoter polymorphism does not act as a strong susceptibility factor for TLE+HS in a population of individuals of European ancestry.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Epilepsy, Temporal Lobe / diagnosis
  • Epilepsy, Temporal Lobe / epidemiology
  • Epilepsy, Temporal Lobe / genetics*
  • Ethnicity / genetics
  • Europe / ethnology
  • Gene Frequency / genetics
  • Genetic Predisposition to Disease
  • Genetic Variation*
  • Genotype
  • Hippocampus / pathology
  • Humans
  • Interleukin-1 / genetics*
  • Interleukin-1beta
  • Peptide Fragments / genetics*
  • Phenotype
  • Polymorphism, Genetic / genetics
  • Promoter Regions, Genetic / genetics
  • Sclerosis
  • United States / epidemiology
  • White People / genetics

Substances

  • Interleukin-1
  • Interleukin-1beta
  • Peptide Fragments
  • interleukin-1beta (163-171)