Neurobiology Research Unit and Center for Integrated Molecular Brain Imaging, Denmark.
Neuropsychopharmacology. 2010 Apr;35(5):1129-37. doi: 10.1038/npp.2009.218. Epub 2009 Dec 30.
Life stress is a robust risk factor for later development of mood disorders, particularly for individuals at familial risk. Likewise, scoring high on the personality trait neuroticism is associated with an increased risk for mood disorders. Neuroticism partly reflects stress vulnerability and is positively correlated to frontolimbic serotonin 2A (5-HT(2A)) receptor binding. Here, we investigate whether neuroticism interacts with familial risk in relation to frontolimbic 5-HT(2A) receptor binding. Twenty-one healthy twins with a co-twin history of mood disorder and 16 healthy twins without a co-twin history of mood disorder were included. They answered self-report personality questionnaires and underwent [(18)F]altanserin positron emission tomography. We found a significant interaction between neuroticism and familial risk in predicting the frontolimbic 5-HT(2A) receptor binding (p=0.026) in an analysis adjusting for age and body mass index. Within the high-risk group only, neuroticism and frontolimbic 5-HT(2A) receptor binding was positively associated (p=0.0037). In conclusion, our data indicate that familial risk and neuroticism interact in their relation to frontolimbic 5-HT(2A) receptor binding. These findings point at a plausible neurobiological link between genetic and personality risk factors and vulnerability to developing mood disorders. It contributes to our understanding of why some people at high risk develop mood disorders while others do not. We speculate that an increased stress reactivity in individuals at high familial risk for mood disorders might enhance the effect of neuroticism in shaping the impact of potential environmental stress and thereby influence serotonergic neurotransmission.
生活压力是情绪障碍后期发展的一个强有力的风险因素,尤其是对于有家族风险的个体。同样,神经质人格特质得分高与情绪障碍的风险增加有关。神经质在一定程度上反映了压力易感性,与额眶皮质 5-羟色胺 2A(5-HT2A)受体结合呈正相关。在这里,我们研究神经质是否与家族风险相互作用,与额眶皮质 5-HT2A 受体结合有关。纳入了 21 名有同卵双胞胎心境障碍病史的健康双胞胎和 16 名无同卵双胞胎心境障碍病史的健康双胞胎。他们回答了自我报告的人格问卷,并接受了 [(18)F]altanserin 正电子发射断层扫描。我们发现,在调整年龄和体重指数后,神经质和家族风险在预测额眶皮质 5-HT2A 受体结合方面存在显著的交互作用(p=0.026)。仅在高风险组中,神经质和额眶皮质 5-HT2A 受体结合呈正相关(p=0.0037)。总之,我们的数据表明,家族风险和神经质在与额眶皮质 5-HT2A 受体结合的关系中相互作用。这些发现表明遗传和人格风险因素与易患情绪障碍之间存在合理的神经生物学联系。它有助于我们理解为什么一些处于高风险的人会发展出情绪障碍,而另一些人则不会。我们推测,情绪障碍高家族风险个体的应激反应增加可能会增强神经质在塑造潜在环境应激影响方面的作用,从而影响 5-羟色胺能神经传递。