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威廉姆斯综合征亲社会基因在健康人群中介导催产素反应性和社交焦虑。

The Williams syndrome prosociality gene mediates oxytocin reactivity and social anxiety in a healthy population.

作者信息

Procyshyn Tanya L, Spence Jason, Read Silven, Watson Neil V, Crespi Bernard J

机构信息

Department of Biological Sciences, Simon Fraser University, 8888 University Drive, Burnaby, Canada V5A 1S6.

Department of Psychology, Simon Fraser University, 8888 University Drive, Burnaby, Canada V5A 1S6.

出版信息

Biol Lett. 2017 Apr;13(4). doi: 10.1098/rsbl.2017.0051.

DOI:10.1098/rsbl.2017.0051
PMID:28424317
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5414696/
Abstract

The neurohormone oxytocin plays a central role in human social behaviour and cognition, and oxytocin dysregulation may contribute to psychiatric disorders. However, genetic factors influencing individual variation in the oxytocinergic system remain poorly understood. We genotyped 169 healthy adults for a functional polymorphism in (), a gene associated with high prosociality and reduced social anxiety in Williams syndrome, a condition reported to involve high oxytocin levels and reactivity. Participants' salivary oxytocin levels were measured before and after watching a validated empathy-inducing video. Oxytocin reactivity, defined as pre- to post-video percentage change in salivary oxytocin, varied substantially and significantly between individuals with different genotypes, with, additionally, a trend towards an interaction between genotype and sex. Individuals with more oxytocin-reactive genotypes also reported significantly lower social anxiety. These findings suggest a model whereby has a continuum of effects on human sociality, from the extreme social phenotypes and oxytocin dysregulation associated with gene deletion in Williams syndrome, to individual differences in oxytocin reactivity and sociality associated with common polymorphisms in healthy populations.

摘要

神经激素催产素在人类社会行为和认知中起着核心作用,催产素失调可能导致精神疾病。然而,影响催产素能系统个体差异的遗传因素仍知之甚少。我们对169名健康成年人进行了基因分型,检测了()基因中的一个功能多态性,该基因与威廉姆斯综合征中的高度亲社会行为和社交焦虑降低有关,据报道,威廉姆斯综合征患者的催产素水平和反应性较高。在观看一段经过验证的引发同理心的视频前后,测量了参与者的唾液催产素水平。催产素反应性定义为视频前后唾液催产素的百分比变化,在不同基因型的个体之间有很大且显著的差异,此外,基因型和性别之间还有相互作用的趋势。催产素反应性基因型较多的个体也报告社交焦虑显著较低。这些发现表明了一种模式,即()基因对人类社交性有连续的影响,从与威廉姆斯综合征基因缺失相关的极端社会表型和催产素失调,到与健康人群常见多态性相关的催产素反应性和社交性的个体差异。

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本文引用的文献

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Role of Splice Variants of Gtf2i, a Transcription Factor Localizing at Postsynaptic Sites, and Its Relation to Neuropsychiatric Diseases.定位于突触后位点的转录因子Gtf2i的剪接变体的作用及其与神经精神疾病的关系。
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A Common Polymorphism in a Williams Syndrome Gene Predicts Amygdala Reactivity and Extraversion in Healthy Adults.威廉姆斯综合征基因中的一种常见多态性可预测健康成年人的杏仁核反应性和外向性。
Biol Psychiatry. 2017 Feb 1;81(3):203-210. doi: 10.1016/j.biopsych.2015.12.007. Epub 2015 Dec 15.
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Variation in the Williams syndrome GTF2I gene and anxiety proneness interactively affect prefrontal cortical response to aversive stimuli.威廉姆斯综合征GTF2I基因的变异与焦虑倾向相互作用,影响前额叶皮质对厌恶刺激的反应。
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Oxytocin, testosterone, and human social cognition.催产素、睾丸素与人类社会认知。
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Cognitive-behavioral phenotypes of Williams syndrome are associated with genetic variation in the GTF2I gene, in a healthy population.在健康人群中,威廉姆斯综合征的认知行为表型与GTF2I基因的遗传变异有关。
BMC Neurosci. 2014 Nov 28;15:127. doi: 10.1186/s12868-014-0127-1.
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Parent-child interaction and oxytocin production in pre-schoolers with autism spectrum disorder.自闭症谱系障碍学龄前儿童的亲子互动与催产素产生。
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