Genetic variation in BDNF is associated with antipsychotic treatment resistance in patients with schizophrenia. Academic Article uri icon

Overview

abstract

  • OBJECTIVE: Antipsychotic drugs are the mainstay of treatment for schizophrenia. However, a substantial proportion of patients are poorly responsive or resistant to first-line treatments, and clozapine treatment is often indicated. Therefore, we and others have used clozapine treatment as a proxy phenotype for antipsychotic treatment resistance in pharmacogenetic studies. In the present study, we utilized this phenotype to test previously-identified candidate genes for antipsychotic treatment response. METHOD: We assessed 89 Caucasian schizophrenia patients clinically assigned to clozapine treatment versus 190 Caucasian patients that were not selected for clozapine treatment. We conducted gene-based association tests on a set of 74 relevant candidate genes nominated in the CATIE pharmacogenetic study (Need et al., 2009), using the GATES procedure (Li et al., 2011). RESULTS: After correcting for multiple testing in the gene-based association test, the gene for brain derived neurotrophic factor (BDNF) was significantly associated with treatment resistance. The top single nucleotide polymorphisms (SNPs) in BDNF included rs11030104 (OR = 2.57), rs10501087 (OR = 2.19) and rs6265 (Val66Met) (OR = 2.08). These SNPs appear to be in high linkage disequilibrium with each other. CONCLUSION: BDNF appears to have a strong association with antipsychotic treatment resistance. Future studies are needed to replicate this finding and further elucidate the biological pathways underlying the association between BDNF and antipsychotic drug response.

publication date

  • February 19, 2013

Research

keywords

  • Antipsychotic Agents
  • Brain-Derived Neurotrophic Factor
  • Clozapine
  • Pharmacogenetics
  • Polymorphism, Single Nucleotide
  • Schizophrenia

Identity

PubMed Central ID

  • PMC3622803

Scopus Document Identifier

  • 84875914963

Digital Object Identifier (DOI)

  • 10.1016/j.schres.2013.01.020

PubMed ID

  • 23433505

Additional Document Info

volume

  • 146

issue

  • 1-3