Failure to find association between febrile seizures and SCN1A rs3812718 polymorphism in south Indian patients with mesial temporal lobe epilepsy and hippocampal sclerosis

Epilepsy Res. 2012 Sep;101(3):288-92. doi: 10.1016/j.eplepsyres.2012.04.009. Epub 2012 May 10.

Abstract

We compared the allele and genotype frequencies of SCN1A SNP rs3812718 between patients with MTLE-HS of south Indian ancestry with and without febrile seizures (FS) and with ethnically matched controls. While we observed no significant difference in allele and genotype frequencies of rs3812718 between MTLE-HS patients with and without FS, A allele and AA genotype were overrepresented in MTLE-HS patients when compared to controls. We conclude that in the population studied, although rs3812718 polymorphism increases the susceptibility to MTLE-HS, this is not by increasing the susceptibility to FS.

MeSH terms

  • Adult
  • Alleles
  • Epilepsy, Temporal Lobe / genetics*
  • Epilepsy, Temporal Lobe / pathology
  • Female
  • Gene Frequency
  • Genetic Association Studies
  • Hippocampus / pathology*
  • Humans
  • India
  • Male
  • Middle Aged
  • NAV1.1 Voltage-Gated Sodium Channel / genetics*
  • Polymorphism, Single Nucleotide
  • Sclerosis / pathology
  • Seizures, Febrile / genetics*
  • Seizures, Febrile / pathology
  • White People / genetics

Substances

  • NAV1.1 Voltage-Gated Sodium Channel
  • SCN1A protein, human