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Abstract 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.
AbstractList 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.
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.
Abstract 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.
Audience Academic
Author Tyni, Sasu
Ojansuu, Ilkka
Koskuvi, Marja
Lehtonen, Šárka
Virtanen, Pekka L. J.
Paunio, Tiina
Hyötyläinen, Ida
Repo-Tiihonen, Eila
Rautiainen, Marja-Riitta
Vaurio, Olli
Lähteenvuo, Markku
Tiihonen, Jari
Gao, Yanyan
Koistinaho, Jari
Puttonen, Katja A.
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  surname: Gao
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  givenname: Tiina
  surname: Paunio
  fullname: Paunio, Tiina
  organization: Department of Mental Health and Substance Abuse Services and Public Health Genomics Unit, National Institute for Health and Welfare, Institute of Clinical Medicine, Department of Psychiatry, University of Helsinki, Department of Psychiatry, Helsinki University Central Hospital, Finnish Institute of Occupational Health, Development of Work and Work Organizations
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  givenname: Marja-Riitta
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  surname: Lehtonen
  fullname: Lehtonen, Šárka
  email: sarka.lehtonen@uef.fi
  organization: A.I. Virtanen Institute for Molecular Sciences, University of Eastern Finland, Neuroscience Center, Helsinki Institute of Life Science, University of Helsinki
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LA McIntosh (488_CR10) 2017; 69
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Snippet Psychopathy is an extreme form of antisocial behavior, with about 1% prevalence in the general population, and 10–30% among incarcerated criminal offenders....
Psychopathy is an extreme form of antisocial behavior, with about 1% prevalence in the general population, and 10-30% among incarcerated criminal offenders....
Abstract Psychopathy is an extreme form of antisocial behavior, with about 1% prevalence in the general population, and 10–30% among incarcerated criminal...
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SubjectTerms 13/100
631/378
692/699/476
Aggression
Antisocial personality disorder
Antisocial Personality Disorder - genetics
Astrocytes
Autism
Behavioral Sciences
Biological Psychology
Causes of
Criminals
Drug abuse
Emotions
Empathy
Gene expression
Genetic aspects
Glucose metabolism
Heritability
Humans
Immune response
Imprisonment
Medicin och hälsovetenskap
Medicine
Medicine & Public Health
Molecular modelling
Molecular neurobiology
Neurosciences
Neurotransmission
Pharmacotherapy
Psychiatry
Psychological aspects
Social behavior
Sociopathic personality
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