Family-based association study between autism and glutamate receptor 6 gene in Chinese Han trios

Am J Med Genet B Neuropsychiatr Genet. 2004 Nov 15;131B(1):48-50. doi: 10.1002/ajmg.b.30025.

Abstract

The glutamate pathways are involved in diverse processes such as learning and memory, epilepsy, and they play important roles in neural plasticity, neural development, and neurodegeneration. It has been proposed that autism could be a hypoglutamatergic disorder. Recently, Jamain et al. reported that the glutamate receptor 6 (GluR6 or GRIK2) is in linkage disequilibrium with autism. In the present study, the transmission disequilibrium test (TDT) and the haplotype transmission were performed to analyze the four SNPs (SNP1: rs995640; SNP2: rs2227281; SNP3: rs2227283; SNP4: rs2235076) of GluR6 in 174 Chinese Han parent-offspring trios. The TDT demonstrated that the two SNPs (SNP2 and SNP3) showed preferential transmission (TDT P = 0.032). The global chi(2) test for haplotype transmission also revealed an association between GluR6 and autism (chi(2) = 10.78, df = 3, P = 0.013). Our results suggested that GluR6 is in linkage disequilibrium with autism.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Autistic Disorder / genetics*
  • China
  • Family Health
  • Female
  • Gene Frequency
  • Genotype
  • GluK2 Kainate Receptor
  • Haplotypes
  • Humans
  • Linkage Disequilibrium
  • Male
  • Nuclear Family
  • Polymorphism, Single Nucleotide
  • Receptors, Kainic Acid / genetics*

Substances

  • Receptors, Kainic Acid