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The genetic epidemiology of personality disorders

Genetic epidemiologic studies indicate that all ten personality disorders (PDs) classified on the DSM-IV axis II are modestly to moderately heritable. Shared environmental and nonadditive genetic factors are of minor or no importance. No sex differences have been identified. Multivariate studies sug...

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Autor principal: Reichborn-Kjennerud, Ted
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Les Laboratoires Servier 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3181941/
https://www.ncbi.nlm.nih.gov/pubmed/20373672
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author Reichborn-Kjennerud, Ted
author_facet Reichborn-Kjennerud, Ted
author_sort Reichborn-Kjennerud, Ted
collection PubMed
description Genetic epidemiologic studies indicate that all ten personality disorders (PDs) classified on the DSM-IV axis II are modestly to moderately heritable. Shared environmental and nonadditive genetic factors are of minor or no importance. No sex differences have been identified. Multivariate studies suggest that the extensive comorbidity between the PDs can be explained by three common genetic and environmental risk factors. The genetic factors do not reflect the DSM-IV cluster structure, but rather: i) broad vulnerability to PD pathology or negative emotionality; ii) high impulsivity/low agreeableness; and iii) introversion. Common genetic and environmental liability factors contribute to comorbidity between pairs or clusters of axis I and axis II disorders. Molecular genetic studies of PDs, mostly candidate gene association studies, indicate that genes linked to neurotransmitter pathways, especially in the serotonergic and dopaminergic systems, are involved. Future studies, using newer methods like genome-wide association, might take advantage of the use of endophenotypes.
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spelling pubmed-31819412011-10-27 The genetic epidemiology of personality disorders Reichborn-Kjennerud, Ted Dialogues Clin Neurosci Clinical Research Genetic epidemiologic studies indicate that all ten personality disorders (PDs) classified on the DSM-IV axis II are modestly to moderately heritable. Shared environmental and nonadditive genetic factors are of minor or no importance. No sex differences have been identified. Multivariate studies suggest that the extensive comorbidity between the PDs can be explained by three common genetic and environmental risk factors. The genetic factors do not reflect the DSM-IV cluster structure, but rather: i) broad vulnerability to PD pathology or negative emotionality; ii) high impulsivity/low agreeableness; and iii) introversion. Common genetic and environmental liability factors contribute to comorbidity between pairs or clusters of axis I and axis II disorders. Molecular genetic studies of PDs, mostly candidate gene association studies, indicate that genes linked to neurotransmitter pathways, especially in the serotonergic and dopaminergic systems, are involved. Future studies, using newer methods like genome-wide association, might take advantage of the use of endophenotypes. Les Laboratoires Servier 2010-03 /pmc/articles/PMC3181941/ /pubmed/20373672 Text en Copyright: © 2010 LLS http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc-nd/3.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Research
Reichborn-Kjennerud, Ted
The genetic epidemiology of personality disorders
title The genetic epidemiology of personality disorders
title_full The genetic epidemiology of personality disorders
title_fullStr The genetic epidemiology of personality disorders
title_full_unstemmed The genetic epidemiology of personality disorders
title_short The genetic epidemiology of personality disorders
title_sort genetic epidemiology of personality disorders
topic Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3181941/
https://www.ncbi.nlm.nih.gov/pubmed/20373672
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