Dual association of a TRKA polymorphism with schizophrenia

Psychiatr Genet. 2011 Jun;21(3):125-31. doi: 10.1097/YPG.0b013e3283437194.

Abstract

Objective: An interaction between predisposing genes and environmental stressors is thought to underlie the neurodevelopmental disorder schizophrenia. In a targeted gene screening, we previously found that the minor allele of the single nucleotide polymorphism (SNP) rs6336 in the neurotrophic tyrosine kinase receptor 1 (NTRK1/TRKA) gene is associated with schizophrenia as a risk factor.

Methods: We genotyped the TRKA SNP in a total of eight independent Caucasian schizophrenia case-control groups.

Result: Remarkably, although in five of the groups a higher frequency of the risk allele was indeed found in the patients compared with the controls, in the three other groups the SNP acted as a protective factor.

Conclusion: An intriguing possibility is that this dual character of the TRKA SNP is caused by its interaction with endophenotypic and/or epistatic factors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Base Sequence
  • Case-Control Studies
  • DNA Primers
  • Europe
  • Female
  • Genetic Predisposition to Disease
  • Genotype
  • Humans
  • Male
  • Middle Aged
  • Polymerase Chain Reaction
  • Polymorphism, Single Nucleotide*
  • Receptor, trkA / genetics*
  • Schizophrenia / genetics*
  • United States

Substances

  • DNA Primers
  • Receptor, trkA