Effects of interactions between variation in dopaminergic genes, traumatic life events, and anomalous self-experiences on psychosis proneness: Results from a cross-sectional study in a nonclinical sample

Eur Psychiatry. 2020 Nov 20;63(1):e104. doi: 10.1192/j.eurpsy.2020.103.

Abstract

Background: There is a growing number of studies showing interactions between genetic polymorphisms associated with dopaminergic neurotransmission and traumatic life events (TLEs) on a risk of psychotic-like experiences (PLEs). Anomalous self-experiences (ASEs) have been associated both with TLEs as well as with PLEs. However, it remains unknown what is the role of ASEs in the complexity of gene-environment interactions on the emergence of PLEs.

Patients and methods: We included 445 young adults-university students from three big cities in Poland. We used the Traumatic Events Checklist to assess TLEs, the Inventory of Psychotic-Like anomalous self-experiences in order to measure ASEs, and the Prodromal Questionnaire (PQ16) to record the level of PLEs. The following gene polymorphisms, related to dopaminergic neurotransmission, were determined: the catechol-O-methyltransferase (COMT) rs4680 polymorphism, the dopamine D2 receptor (DRD2) rs6277 polymorphism, and the dopamine transporter 1 (DAT1) rs28363170 polymorphism.

Results: There was a significant effect of the interaction between the DAT1 polymorphism, a severity of ASEs, and a history of TLEs on the level of PLEs. Among the DAT1 10R/10R homozygotes with low level of ASEs, a severity of PLEs was significantly higher in individuals with a history of any TLEs. Higher scores of the PQ16 were associated with a greater severity of ASEs both in the DAT1 9R allele carriers and the DAT1 10R/10R homozygotes.

Conclusion: Our findings imply that genetic liability related to aberrant dopamine transport might impact the association between TLEs and PLEs in subjects with high levels of ASEs.

Keywords: Anomalous self-experiences; childhood trauma; psychosis; schizophrenia; stress.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Catechol O-Methyltransferase / metabolism*
  • Cross-Sectional Studies
  • Dopamine / metabolism
  • Female
  • Gene-Environment Interaction
  • Humans
  • Male
  • Poland
  • Polymorphism, Genetic*
  • Psychotic Disorders / genetics
  • Psychotic Disorders / metabolism*
  • Receptors, Dopamine D2 / metabolism
  • Surveys and Questionnaires
  • Young Adult

Substances

  • Receptors, Dopamine D2
  • Catechol O-Methyltransferase
  • Dopamine