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关于损失厌恶的遗传学:脑源性神经营养因子Val66Met与多巴胺D2受体/ANKK1 Taq1a的相互作用效应。

On the genetics of loss aversion: An interaction effect of BDNF Val66Met and DRD2/ANKK1 Taq1a.

作者信息

Voigt Gesine, Montag Christian, Markett Sebastian, Reuter Martin

机构信息

Department of Psychology, University of Bonn.

Department of Psychology, University of Ulm.

出版信息

Behav Neurosci. 2015 Dec;129(6):801-11. doi: 10.1037/bne0000102. Epub 2015 Oct 26.

DOI:10.1037/bne0000102
PMID:26501178
Abstract

Loss aversion is the tendency to overweight losses compared with gains in decision situations. Several studies have investigated the neurobiological background of this phenomenon and it was found that activation in the mesolimbic-mesocortical dopamine system during a gambling decision correlates with loss aversion. In a behavioral experiment with N = 143 subjects, the present study investigates the influence of 2 functional single-nucleotide polymorphisms on the BDNF gene (BDNF Val66Met polymorphism) and ANKK1 gene (DRD2 Taq1a/ANKK1 polymorphism), that are known to affect the dopamine system, on loss aversion. Additionally, associations of alexithymia, a personality construct describing the disability to consciously experience emotions in the self, with loss aversion and with the mentioned polymorphisms were assessed using the TAS-20 questionnaire, to replicate associations that have been reported before. Results revealed a significant interaction effect of the 2 polymorphisms on loss aversion. Carriers of the genetic constellation 66Met+/A1+ had the lowest loss aversion scores, compared with all other allelic groups. According to the literature this allelic configuration is characterized by a relatively low D2/3 receptor binding in the striatum and an impaired activity-dependent secretion of BDNF. This is the first study showing that loss aversion is related to naturally occurring differences in dopamine function.

摘要

损失厌恶是指在决策情境中,相较于收益,人们倾向于过度看重损失。多项研究探讨了这一现象的神经生物学背景,结果发现赌博决策过程中中脑边缘-中脑皮质多巴胺系统的激活与损失厌恶相关。在一项有143名受试者参与的行为实验中,本研究调查了已知会影响多巴胺系统的BDNF基因的两种功能性单核苷酸多态性(BDNF Val66Met多态性)和ANKK1基因(DRD2 Taq1a/ANKK1多态性)对损失厌恶的影响。此外,使用多伦多述情障碍量表(TAS-20)问卷评估了述情障碍(一种描述个体在自我意识中体验情绪存在障碍的人格结构)与损失厌恶以及上述多态性之间的关联,以重复之前报道的关联。结果显示这两种多态性对损失厌恶有显著的交互作用。与所有其他等位基因组相比,遗传组合66Met+/A1+的携带者损失厌恶得分最低。根据文献,这种等位基因配置的特点是纹状体中D2/3受体结合相对较低,且BDNF的活性依赖性分泌受损。这是第一项表明损失厌恶与多巴胺功能的自然差异有关的研究。

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