Hostname: page-component-78c5997874-s2hrs Total loading time: 0 Render date: 2024-11-17T18:20:31.818Z Has data issue: false hasContentIssue false

EPA-1760 – Familial Liability, the BDNF-VAL66MET Polymorphism and Psychotic-Like Experiences

Published online by Cambridge University Press:  15 April 2020

K. Alptekin
Affiliation:
Psychiatry, Dokuz Eylul University, Izmir, Turkey
T. Binbay
Affiliation:
Psychiatry, Dokuz Eylul University, Izmir, Turkey
H. Elbi
Affiliation:
Psychiatry, Ege University, Izmir, Turkey
N. Zagli
Affiliation:
Psychiatry, Ege University, Izmir, Turkey
H. Onay
Affiliation:
Psychiatry, Ege University, Izmir, Turkey
F. Ozkinay
Affiliation:
Psychiatry, Ege University, Izmir, Turkey
J.I.M. Van Os
Affiliation:
Psychiatry, Maastricht University, Maastricht, Netherlands

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.
Background/Objectives

Familial liability to both severe and common mental disorder predicts psychotic disorder, psychotic symptoms and psychotic-like experiences (PLe). However, the relation between familial liability and psychosis outcome may be associated with genetic variation. We investigated the influence of familial liability on PLe in a nonpsychotic, general population based group, and the potential moderating effect of the BDNFVal 66Met polymorphism.

Methods

PLe and familial liability were assessed in 313 individuals (mean age 38.6±13.3; gender: 43% males). Familial liability was obtained using the questions from Family Interview for Genetic Studies and dichotomized to none or at least one mental disorder in the first degree relatives (parents and siblings). PLe (visual and auditory hallucinations) were assessed through relevant questions in CIDI 2.1 G section on psychotic disorders. The sample undergone clinical reinterviews with the Structured Clinical Interview for DSMIV. BDNF val66met (rs6265) was genotyped using standardized procedures.

Results

Familial liability was associated with PLe (OR= 1.8; CI: 1.1–3.0; p: 0.012). The association between familial liability and PLe was significant in individuals with Val/Val allele (OR= 2.2; CI: 1.2-4.1; p: 0.009) whereas there was no evidence for an association between familial liability and PLe in Met carrier individuals.

Conclusion

Individuals with a familial liability for mental disorders are more likely to report PLe. Val/Val genotype reported more PLe when exposed to familial liability than did individuals carrying Met allele. Therefore, the observed gene-environment interaction effect may be partially responsible for individual variation in response to familial liability.

Type
P31 - Schizophrenia
Copyright
Copyright © European Psychiatric Association 2014
Submit a response

Comments

No Comments have been published for this article.