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
Department of Forensic Psychiatry, Niuvanniemi Hospital, University of Eastern Finland, Niuvankuja 65, FI-70240, Kuopio, Finland.
Karolinska Institutet, Department of Clinical Neuroscience, Centre for Psychiatry Research, Stockholm County Council, Byggnad R5, SE-171 77, Stockholm, Sweden.
Mol Psychiatry. 2020 Dec;25(12):3432-3441. doi: 10.1038/s41380-019-0488-z. Epub 2019 Aug 27.
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.
精神病态是一种极端的反社会行为形式,在普通人群中的患病率约为1%,在被监禁的刑事罪犯中为10 - 30%。尽管严重反社会行为的遗传度高达50%,但其遗传背景尚不清楚。潜在的分子机制仍然未知,但先前的几项研究表明,异常的葡萄糖代谢和阿片样物质神经传递与暴力犯罪和精神病态有关。在这里,我们使用来自六名被监禁的极端反社会和暴力罪犯、三名有药物滥用问题的非精神病态个体以及六名健康对照的诱导多能干细胞衍生的皮质神经元和星形胶质细胞表明,存在几种特定于精神病态的基因表达和免疫反应相关分子途径的强烈改变。在神经元中,精神病态与RPL10P9和ZNF132的显著上调以及CDH5和OPRD1的下调有关。在星形胶质细胞中,RPL10P9和MT - RNR2上调。上述基因的表达解释了精神病态症状30 - 92%的变异。基因表达结果通过定量聚合酶链反应得到证实。这些基因可能与精神病态中缺乏同理心和情感冷漠有关,因为几项研究已将这些基因与自闭症和社交互动联系起来。