Cargando…

Genetic overlap between psychotic experiences in the community across age and with psychiatric disorders

This study explores the degree to which genetic influences on psychotic experiences are stable across adolescence and adulthood, and their overlap with psychiatric disorders. Genome-wide association results were obtained for adolescent psychotic experiences and negative symptom traits (N = 6297–10,0...

Descripción completa

Detalles Bibliográficos
Autores principales: Barkhuizen, Wikus, Pain, Oliver, Dudbridge, Frank, Ronald, Angelica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7062754/
https://www.ncbi.nlm.nih.gov/pubmed/32152294
http://dx.doi.org/10.1038/s41398-020-0765-2
_version_ 1783504574108139520
author Barkhuizen, Wikus
Pain, Oliver
Dudbridge, Frank
Ronald, Angelica
author_facet Barkhuizen, Wikus
Pain, Oliver
Dudbridge, Frank
Ronald, Angelica
author_sort Barkhuizen, Wikus
collection PubMed
description This study explores the degree to which genetic influences on psychotic experiences are stable across adolescence and adulthood, and their overlap with psychiatric disorders. Genome-wide association results were obtained for adolescent psychotic experiences and negative symptom traits (N = 6297–10,098), schizotypy (N = 3967–4057) and positive psychotic experiences in adulthood (N = 116,787–117,794), schizophrenia (N = 150,064), bipolar disorder (N = 41,653), and depression (N = 173,005). Linkage disequilibrium score regression was used to estimate genetic correlations. Implicated genes from functional and gene-based analyses were compared. Mendelian randomization was performed on trait pairs with significant genetic correlations. Results indicated that subclinical auditory and visual hallucinations and delusions of persecution during adulthood were significantly genetically correlated with schizophrenia (r(g) = 0.27–0.67) and major depression (r(g) = 0.41–96) after correction for multiple testing. Auditory and visual subclinical hallucinations were highly genetically correlated (r(g) = 0.95). Cross-age genetic correlations for psychotic experiences were not significant. Gene mapping and association analyses revealed 14 possible genes associated with psychotic experiences that overlapped across age for psychotic experiences or between psychotic experiences and psychiatric disorders. Mendelian randomization indicated bidirectional associations between auditory and visual hallucinations in adults but did not support causal relationships between psychotic experiences and psychiatric disorders. These findings indicate that psychotic experiences in adulthood may be more linked genetically to schizophrenia and major depression than psychotic experiences in adolescence. Our study implicated specific genes that are associated with psychotic experiences across development, as well as genes shared between psychotic experiences and psychiatric disorders.
format Online
Article
Text
id pubmed-7062754
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-70627542020-03-19 Genetic overlap between psychotic experiences in the community across age and with psychiatric disorders Barkhuizen, Wikus Pain, Oliver Dudbridge, Frank Ronald, Angelica Transl Psychiatry Article This study explores the degree to which genetic influences on psychotic experiences are stable across adolescence and adulthood, and their overlap with psychiatric disorders. Genome-wide association results were obtained for adolescent psychotic experiences and negative symptom traits (N = 6297–10,098), schizotypy (N = 3967–4057) and positive psychotic experiences in adulthood (N = 116,787–117,794), schizophrenia (N = 150,064), bipolar disorder (N = 41,653), and depression (N = 173,005). Linkage disequilibrium score regression was used to estimate genetic correlations. Implicated genes from functional and gene-based analyses were compared. Mendelian randomization was performed on trait pairs with significant genetic correlations. Results indicated that subclinical auditory and visual hallucinations and delusions of persecution during adulthood were significantly genetically correlated with schizophrenia (r(g) = 0.27–0.67) and major depression (r(g) = 0.41–96) after correction for multiple testing. Auditory and visual subclinical hallucinations were highly genetically correlated (r(g) = 0.95). Cross-age genetic correlations for psychotic experiences were not significant. Gene mapping and association analyses revealed 14 possible genes associated with psychotic experiences that overlapped across age for psychotic experiences or between psychotic experiences and psychiatric disorders. Mendelian randomization indicated bidirectional associations between auditory and visual hallucinations in adults but did not support causal relationships between psychotic experiences and psychiatric disorders. These findings indicate that psychotic experiences in adulthood may be more linked genetically to schizophrenia and major depression than psychotic experiences in adolescence. Our study implicated specific genes that are associated with psychotic experiences across development, as well as genes shared between psychotic experiences and psychiatric disorders. Nature Publishing Group UK 2020-03-09 /pmc/articles/PMC7062754/ /pubmed/32152294 http://dx.doi.org/10.1038/s41398-020-0765-2 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Barkhuizen, Wikus
Pain, Oliver
Dudbridge, Frank
Ronald, Angelica
Genetic overlap between psychotic experiences in the community across age and with psychiatric disorders
title Genetic overlap between psychotic experiences in the community across age and with psychiatric disorders
title_full Genetic overlap between psychotic experiences in the community across age and with psychiatric disorders
title_fullStr Genetic overlap between psychotic experiences in the community across age and with psychiatric disorders
title_full_unstemmed Genetic overlap between psychotic experiences in the community across age and with psychiatric disorders
title_short Genetic overlap between psychotic experiences in the community across age and with psychiatric disorders
title_sort genetic overlap between psychotic experiences in the community across age and with psychiatric disorders
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7062754/
https://www.ncbi.nlm.nih.gov/pubmed/32152294
http://dx.doi.org/10.1038/s41398-020-0765-2
work_keys_str_mv AT barkhuizenwikus geneticoverlapbetweenpsychoticexperiencesinthecommunityacrossageandwithpsychiatricdisorders
AT painoliver geneticoverlapbetweenpsychoticexperiencesinthecommunityacrossageandwithpsychiatricdisorders
AT dudbridgefrank geneticoverlapbetweenpsychoticexperiencesinthecommunityacrossageandwithpsychiatricdisorders
AT ronaldangelica geneticoverlapbetweenpsychoticexperiencesinthecommunityacrossageandwithpsychiatricdisorders