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Neurobiological roots of psychopathy

Psychopathy is an extreme form of antisocial behavior, with about 1% prevalence in the general population, and 10–30% among incarcerated criminal offenders. Although the heritability of severe antisocial behavior is up to 50%, the genetic background is unclear. The underlying molecular mechanisms ha...

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Autores principales: Tiihonen, Jari, Koskuvi, Marja, Lähteenvuo, Markku, Virtanen, Pekka L. J., Ojansuu, Ilkka, Vaurio, Olli, Gao, Yanyan, Hyötyläinen, Ida, Puttonen, Katja A., Repo-Tiihonen, Eila, Paunio, Tiina, Rautiainen, Marja-Riitta, Tyni, Sasu, Koistinaho, Jari, Lehtonen, Šárka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7714686/
https://www.ncbi.nlm.nih.gov/pubmed/31455857
http://dx.doi.org/10.1038/s41380-019-0488-z
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author Tiihonen, Jari
Koskuvi, Marja
Lähteenvuo, Markku
Virtanen, Pekka L. J.
Ojansuu, Ilkka
Vaurio, Olli
Gao, Yanyan
Hyötyläinen, Ida
Puttonen, Katja A.
Repo-Tiihonen, Eila
Paunio, Tiina
Rautiainen, Marja-Riitta
Tyni, Sasu
Koistinaho, Jari
Lehtonen, Šárka
author_facet Tiihonen, Jari
Koskuvi, Marja
Lähteenvuo, Markku
Virtanen, Pekka L. J.
Ojansuu, Ilkka
Vaurio, Olli
Gao, Yanyan
Hyötyläinen, Ida
Puttonen, Katja A.
Repo-Tiihonen, Eila
Paunio, Tiina
Rautiainen, Marja-Riitta
Tyni, Sasu
Koistinaho, Jari
Lehtonen, Šárka
author_sort Tiihonen, Jari
collection PubMed
description Psychopathy is an extreme form of antisocial behavior, with about 1% prevalence in the general population, and 10–30% among incarcerated criminal offenders. Although the heritability of severe antisocial behavior is up to 50%, the genetic background is unclear. The underlying molecular mechanisms have remained unknown but several previous studies suggest that abnormal glucose metabolism and opioidergic neurotransmission contribute to violent offending and psychopathy. Here we show using iPSC-derived cortical neurons and astrocytes from six incarcerated extremely antisocial and violent offenders, three nonpsychopathic individuals with substance abuse, and six healthy controls that there are robust alterations in the expression of several genes and immune response-related molecular pathways which were specific for psychopathy. In neurons, psychopathy was associated with marked upregulation of RPL10P9 and ZNF132, and downregulation of CDH5 and OPRD1. In astrocytes, RPL10P9 and MT-RNR2 were upregulated. Expression of aforementioned genes explained 30–92% of the variance of psychopathic symptoms. The gene expression findings were confirmed with qPCR. These genes may be relevant to the lack of empathy and emotional callousness seen in psychopathy, since several studies have linked these genes to autism and social interaction.
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spelling pubmed-77146862020-12-11 Neurobiological roots of psychopathy Tiihonen, Jari Koskuvi, Marja Lähteenvuo, Markku Virtanen, Pekka L. J. Ojansuu, Ilkka Vaurio, Olli Gao, Yanyan Hyötyläinen, Ida Puttonen, Katja A. Repo-Tiihonen, Eila Paunio, Tiina Rautiainen, Marja-Riitta Tyni, Sasu Koistinaho, Jari Lehtonen, Šárka Mol Psychiatry Article Psychopathy is an extreme form of antisocial behavior, with about 1% prevalence in the general population, and 10–30% among incarcerated criminal offenders. Although the heritability of severe antisocial behavior is up to 50%, the genetic background is unclear. The underlying molecular mechanisms have remained unknown but several previous studies suggest that abnormal glucose metabolism and opioidergic neurotransmission contribute to violent offending and psychopathy. Here we show using iPSC-derived cortical neurons and astrocytes from six incarcerated extremely antisocial and violent offenders, three nonpsychopathic individuals with substance abuse, and six healthy controls that there are robust alterations in the expression of several genes and immune response-related molecular pathways which were specific for psychopathy. In neurons, psychopathy was associated with marked upregulation of RPL10P9 and ZNF132, and downregulation of CDH5 and OPRD1. In astrocytes, RPL10P9 and MT-RNR2 were upregulated. Expression of aforementioned genes explained 30–92% of the variance of psychopathic symptoms. The gene expression findings were confirmed with qPCR. These genes may be relevant to the lack of empathy and emotional callousness seen in psychopathy, since several studies have linked these genes to autism and social interaction. Nature Publishing Group UK 2019-08-27 2020 /pmc/articles/PMC7714686/ /pubmed/31455857 http://dx.doi.org/10.1038/s41380-019-0488-z Text en © The Author(s) 2019 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
Tiihonen, Jari
Koskuvi, Marja
Lähteenvuo, Markku
Virtanen, Pekka L. J.
Ojansuu, Ilkka
Vaurio, Olli
Gao, Yanyan
Hyötyläinen, Ida
Puttonen, Katja A.
Repo-Tiihonen, Eila
Paunio, Tiina
Rautiainen, Marja-Riitta
Tyni, Sasu
Koistinaho, Jari
Lehtonen, Šárka
Neurobiological roots of psychopathy
title Neurobiological roots of psychopathy
title_full Neurobiological roots of psychopathy
title_fullStr Neurobiological roots of psychopathy
title_full_unstemmed Neurobiological roots of psychopathy
title_short Neurobiological roots of psychopathy
title_sort neurobiological roots of psychopathy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7714686/
https://www.ncbi.nlm.nih.gov/pubmed/31455857
http://dx.doi.org/10.1038/s41380-019-0488-z
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