Department of Cognitive Psychology II, Johann Wolfgang Goethe University Frankfurt/Main, Germany.
Department of Neurodegeneration, Hertie Institute for Clinical Brain Research, Tübingen, Germany.
Neuroimage. 2013 Nov 1;81:393-399. doi: 10.1016/j.neuroimage.2013.05.037. Epub 2013 May 16.
Gray's Reinforcement Sensitivity Theory (RST) has developed into one of the most prominent personality theories of the last decades. The RST postulates a Behavioral Inhibition System (BIS) modulating the reaction to stimuli indicating aversive events. A number of psychiatric disorders including depression, anxiety disorders, and psychosomatic illnesses have been associated with extreme BIS responsiveness. In recent years, neuroimaging studies have implicated the amygdala-septo-hippocampal circuit as an important neural substrate of the BIS. However, the neurogenetic basis of the regulation of this behaviorally and clinically essential system remains unclear. Investigating the effects of two functional genetic polymorphisms (tryptophan hydroxylase-2, G-703T, and serotonin transporter, serotonin transporter gene-linked polymorphic region) in 89 human participants, we find significantly different patterns of associations between BIS scores and amygdala-hippocampus connectivity during loss anticipation for genotype groups regarding both polymorphisms. Specifically, the correlation between amygdala-hippocampus connectivity and Gray's trait anxiety scores is positive in individuals homozygous for the TPH2 G-allele, while carriers of at least one T-allele show a negative association. Likewise, individuals homozygous for the 5-HTTLPR L(A) variant display a positive association while carriers of the S/L(G) allele show a trend towards a negative association. Thus, we show converging evidence of different neural implementation of the BIS depending on genotype-dependent levels of serotonin. We provide evidence suggesting that genotype-dependent serotonin levels and thus putative changes in the efficiency of serotonergic neurotransmission might not only alter brain activation levels directly, but also more fundamentally impact the neural implementation of personality traits. We outline the direct clinical implications arising from this finding and discuss the complex interplay of neural responses, genes and personality traits in this context.
格雷的强化敏感性理论(RST)已发展成为过去几十年中最杰出的人格理论之一。该理论假设行为抑制系统(BIS)调节对预示厌恶事件的刺激的反应。许多精神疾病,包括抑郁症、焦虑症和身心疾病,都与 BIS 反应过度有关。近年来,神经影像学研究表明,杏仁核-隔-海马回路是 BIS 的重要神经基础。然而,调节这种行为和临床重要系统的神经遗传基础仍不清楚。在 89 名人类参与者中,我们研究了两种功能性遗传多态性(色氨酸羟化酶-2,G-703T 和 5-羟色胺转运体,5-羟色胺转运体基因连锁多态区)的影响,发现这两种多态性与基因型群体的损失预期期间 BIS 评分和杏仁核-海马连接之间的关联模式存在显著差异。具体来说,在 TPH2 G-等位基因纯合子个体中,杏仁核-海马连接与格雷特质焦虑评分之间的相关性为正,而至少携带一个 T 等位基因的个体则呈负相关。同样,5-HTTLPR L(A)变体纯合子个体表现出正相关,而 S/L(G)等位基因携带者则表现出负相关的趋势。因此,我们提供了不同的神经实现的 BIS 依赖于基因型依赖的证据表明,5-羟色胺水平的不同神经实现。我们提供的证据表明,基因型依赖的 5-羟色胺水平,以及因此推测的 5-羟色胺能神经传递效率的变化,不仅可能直接改变大脑激活水平,而且更根本地影响人格特质的神经实现。我们概述了这一发现所产生的直接临床意义,并讨论了在这种情况下神经反应、基因和人格特质的复杂相互作用。