Association of GRIN2B gene polymorphism and Obsessive Compulsive disorder and symptom dimensions: A pilot study

Psychiatry Res. 2016 Sep 30:243:152-5. doi: 10.1016/j.psychres.2016.06.027. Epub 2016 Jun 25.

Abstract

The etiology of OCD is largely unknown, but neuroimaging and pharmacological studies suggest that glutamatergic system plays a significant role on OCD development. We genotyped one polymorphism at GRIN2B (rs1019385) by real time Polymerase Chain Reaction in a sample of Brazilian Obsessive-Compulsive patients and healthy controls, and evaluated its influence on OCD. We found the T-allele and TT genotype to be significantly associated with OCD and ordering dimension. The T-allele was also significantly associated with checking. These preliminary results demonstrated that the GRIN2B gene may confer to some extent the susceptibility to OCD and its symptoms.

Keywords: Brazil; Genetics; Symptom dimensions.

MeSH terms

  • Adolescent
  • Adult
  • Alleles*
  • Brazil
  • Female
  • Genetic Association Studies
  • Genetic Predisposition to Disease
  • Genotype*
  • Humans
  • Male
  • Middle Aged
  • Obsessive-Compulsive Disorder / diagnosis
  • Obsessive-Compulsive Disorder / genetics*
  • Pilot Projects
  • Polymorphism, Genetic*
  • Receptors, N-Methyl-D-Aspartate / genetics*
  • Young Adult

Substances

  • NR2B NMDA receptor
  • Receptors, N-Methyl-D-Aspartate