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A polymorphism in the dysbindin gene (DTNBP1) associated with multiple psychiatric disorders including schizophrenia

BACKGROUND: A number of studies have found associations between dysbindin (DTNBP1) polymorphisms and schizophrenia. Recently we identified a DTNBP1 SNP (rs9370822) that is strongly associated with schizophrenia. Individuals diagnosed with schizophrenia were nearly three times as likely to carry the...

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Autores principales: Voisey, Joanne, Swagell, Christopher D, Hughes, Ian P, Connor, Jason P, Lawford, Bruce R, Young, Ross M, Morris, C Phillip
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2911395/
https://www.ncbi.nlm.nih.gov/pubmed/20615259
http://dx.doi.org/10.1186/1744-9081-6-41
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author Voisey, Joanne
Swagell, Christopher D
Hughes, Ian P
Connor, Jason P
Lawford, Bruce R
Young, Ross M
Morris, C Phillip
author_facet Voisey, Joanne
Swagell, Christopher D
Hughes, Ian P
Connor, Jason P
Lawford, Bruce R
Young, Ross M
Morris, C Phillip
author_sort Voisey, Joanne
collection PubMed
description BACKGROUND: A number of studies have found associations between dysbindin (DTNBP1) polymorphisms and schizophrenia. Recently we identified a DTNBP1 SNP (rs9370822) that is strongly associated with schizophrenia. Individuals diagnosed with schizophrenia were nearly three times as likely to carry the CC genotype compared to the AA genotype. METHODS: To investigate the importance of this SNP in the function of DTNBP1, a number of psychiatric conditions including addictive behaviours and anxiety disorders were analysed for association with rs9370822. RESULTS: The DTNBP1 polymorphism was significantly associated with post-traumatic stress disorder (PTSD) as well as nicotine and opiate dependence but not alcohol dependence. Individuals suffering PTSD were more than three times as likely to carry the CC genotype compared to the AA genotype. Individuals with nicotine or opiate dependence were more than twice as likely to carry the CC genotype compared to the AA genotype. CONCLUSIONS: This study provides further support for the importance of DTNBP1 in psychiatric conditions and suggests that there is a common underlying molecular defect involving DTNBP1 that contributes to the development of several anxiety and addictive disorders that are generally recognised as separate clinical conditions. These disorders may actually be different expressions of a single metabolic pathway perturbation. As our participant numbers are limited our observations should be viewed with caution until they are independently replicated.
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spelling pubmed-29113952010-07-29 A polymorphism in the dysbindin gene (DTNBP1) associated with multiple psychiatric disorders including schizophrenia Voisey, Joanne Swagell, Christopher D Hughes, Ian P Connor, Jason P Lawford, Bruce R Young, Ross M Morris, C Phillip Behav Brain Funct Research BACKGROUND: A number of studies have found associations between dysbindin (DTNBP1) polymorphisms and schizophrenia. Recently we identified a DTNBP1 SNP (rs9370822) that is strongly associated with schizophrenia. Individuals diagnosed with schizophrenia were nearly three times as likely to carry the CC genotype compared to the AA genotype. METHODS: To investigate the importance of this SNP in the function of DTNBP1, a number of psychiatric conditions including addictive behaviours and anxiety disorders were analysed for association with rs9370822. RESULTS: The DTNBP1 polymorphism was significantly associated with post-traumatic stress disorder (PTSD) as well as nicotine and opiate dependence but not alcohol dependence. Individuals suffering PTSD were more than three times as likely to carry the CC genotype compared to the AA genotype. Individuals with nicotine or opiate dependence were more than twice as likely to carry the CC genotype compared to the AA genotype. CONCLUSIONS: This study provides further support for the importance of DTNBP1 in psychiatric conditions and suggests that there is a common underlying molecular defect involving DTNBP1 that contributes to the development of several anxiety and addictive disorders that are generally recognised as separate clinical conditions. These disorders may actually be different expressions of a single metabolic pathway perturbation. As our participant numbers are limited our observations should be viewed with caution until they are independently replicated. BioMed Central 2010-07-09 /pmc/articles/PMC2911395/ /pubmed/20615259 http://dx.doi.org/10.1186/1744-9081-6-41 Text en Copyright ©2010 Voisey et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Voisey, Joanne
Swagell, Christopher D
Hughes, Ian P
Connor, Jason P
Lawford, Bruce R
Young, Ross M
Morris, C Phillip
A polymorphism in the dysbindin gene (DTNBP1) associated with multiple psychiatric disorders including schizophrenia
title A polymorphism in the dysbindin gene (DTNBP1) associated with multiple psychiatric disorders including schizophrenia
title_full A polymorphism in the dysbindin gene (DTNBP1) associated with multiple psychiatric disorders including schizophrenia
title_fullStr A polymorphism in the dysbindin gene (DTNBP1) associated with multiple psychiatric disorders including schizophrenia
title_full_unstemmed A polymorphism in the dysbindin gene (DTNBP1) associated with multiple psychiatric disorders including schizophrenia
title_short A polymorphism in the dysbindin gene (DTNBP1) associated with multiple psychiatric disorders including schizophrenia
title_sort polymorphism in the dysbindin gene (dtnbp1) associated with multiple psychiatric disorders including schizophrenia
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2911395/
https://www.ncbi.nlm.nih.gov/pubmed/20615259
http://dx.doi.org/10.1186/1744-9081-6-41
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