[Association polymorphic variants of GRIN2B gene with paranoid schizophrenia and response to common neuroleptics in Russians and Tatars from Bashkortostan Republic]

Genetika. 2013 Sep;49(9):1106-13. doi: 10.7868/s001667581308002x.
[Article in Russian]

Abstract

An analysis of the association of paranoid schizophrenia seeking with polymorphic variants of GRIN2B gene was performed in order to identify genetic risk factors of disease development and genetic markers of the response to therapy by neuroleptics in Russian and Tatar patients from Bashkortostan Republic (BB). In the course of the analysis, we revealed the following: 1) genetic markers of increased risk of developing paranoid schizophrenia in various ethnic groups, including, in Tatars, the GRIN2B* T/*Tgenotype (p = 0.003; OR = 2.33) and GRIN2B*T allele (p = 0.001; OR = 2.36), rs1805247; in Russians, the GRIN2B*T/*T genotype (p = 0.038; OR = 2.12) and GRIN2B* T allele (p = 0.028; OR = 2.03), rs1805247, genotype GRIN2B*A/*A (p = 0.042; OR = 2.12), rs1805476; 2) genetic markers of the reduced risk of developing paranoid schizophrenia; 3) genetic markers of therapy response and the risk of side effects development during neuroleptics (haloperidol) treatment in Bashkortostan. The significant interethnic diversity of genetic factors related to the risk of this disease development was noted.

MeSH terms

  • Adult
  • Antipsychotic Agents / therapeutic use*
  • Bashkiria / ethnology
  • Case-Control Studies
  • Ethnicity / genetics
  • Female
  • Gene Frequency
  • Genetic Markers
  • Genetic Predisposition to Disease
  • Haplotypes
  • Humans
  • Male
  • Middle Aged
  • Polymorphism, Genetic
  • Polymorphism, Single Nucleotide
  • Receptors, N-Methyl-D-Aspartate / genetics*
  • Schizophrenia, Paranoid / drug therapy*
  • Schizophrenia, Paranoid / genetics*
  • Treatment Outcome
  • White People / genetics

Substances

  • Antipsychotic Agents
  • Genetic Markers
  • NR2B NMDA receptor
  • Receptors, N-Methyl-D-Aspartate