The Dopamine D3 receptor gene and posttraumatic stress disorder

Erika J. Wolf, Karen S. Mitchell, Mark W. Logue, Clinton T. Baldwin, Annemarie F. Reardon, Alison Aiello, Sandro Galea, Karestan C. Koenen, Monica Uddin, Derek Wildman, Mark W. Miller

Research output: Contribution to journalArticlepeer-review

Abstract

The dopamine D3 receptor (DRD3) gene has been implicated in schizophrenia, autism, and substance use-disorders and is related to emotion reactivity, executive functioning, and stress-responding, processes impaired in posttraumatic stress disorder (PTSD). The aim of this candidate gene study was to evaluate DRD3 polymorphisms for association with PTSD. The discovery sample was trauma-exposed White, non-Hispanic U.S. veterans and their trauma-exposed intimate partners (N = 491); 60.3% met criteria for lifetime PTSD. The replication sample was 601 trauma-exposed African American participants living in Detroit, Michigan; 23.6% met criteria for lifetime PTSD. Genotyping was based on high-density bead chips. In the discovery sample, 4 single nucleotide polymorphisms (SNPs), rs2134655, rs201252087, rs4646996, and rs9868039, showed evidence of association with PTSD and withstood correction for multiple testing. The minor alleles were associated with reduced risk for PTSD (OR range = 0.59 to 0.69). In the replication sample, rs2251177, located 149 base pairs away from the most significant SNP in the discovery sample, was nominally associated with PTSD in men (OR = 0.32). Although the precise role of the D3 receptor in PTSD is not yet known, its role in executive functioning and emotional reactivity, and the sensitivity of the dopamine system to environmental stressors could potentially explain this association.

Original languageEnglish (US)
Pages (from-to)379-387
Number of pages9
JournalJournal of Traumatic Stress
Volume27
Issue number4
DOIs
StatePublished - Aug 2014

ASJC Scopus subject areas

  • Clinical Psychology
  • Psychiatry and Mental health

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