Developmental Neuroimaging and Psychopathology Laboratory, Department of Psychiatry, Massachusetts General Hospital, Boston, MA 02114, USA.
Mol Psychiatry. 2012 Oct;17(10):1042-50. doi: 10.1038/mp.2011.96. Epub 2011 Sep 6.
One of the central questions that has occupied those disciplines concerned with human development is the nature of continuities and discontinuities from birth to maturity. The amygdala has a central role in the processing of novelty and emotion in the brain. Although there is considerable variability among individuals in the reactivity of the amygdala to novel and emotional stimuli, the origin of these individual differences is not well understood. Four-month old infants called high reactive (HR) demonstrate a distinctive pattern of vigorous motor activity and crying to specific unfamiliar visual, auditory and olfactory stimuli in the laboratory. Low-reactive infants show the complementary pattern. Here, we demonstrate that the HR infant phenotype predicts greater amygdalar reactivity to novel faces almost two decades later in adults. A prediction of individual differences in brain function at maturity can be made on the basis of a single behavioral assessment made in the laboratory at 4 months of age. This is the earliest known human behavioral phenotype that predicts individual differences in patterns of neural activity at maturity. These temperamental differences rooted in infancy may be relevant to understanding individual differences in vulnerability and resilience to clinical psychiatric disorder. Males who were HR infants showed particularly high levels of reactivity to novel faces in the amygdala that distinguished them as adults from all other sex/temperament subgroups, suggesting that their amygdala is particularly prone to engagement by unfamiliar faces. These findings underline the importance of taking gender into account when studying the developmental neurobiology of human temperament and anxiety disorders. The genetic study of behavioral and biologic intermediate phenotypes (or 'endophenotypes') indexing anxiety-proneness offers an important alternative to examining phenotypes based on clinically defined disorder. As the HR phenotype is characterized by specific patterns of reactivity to elemental visual, olfactory and auditory stimuli, well before complex social behaviors such as shyness or fearful interaction with strangers can be observed, it may be closer to underlying neurobiological mechanisms than behavioral profiles observed later in life. This possibility, together with the fact that environmental factors have less time to impact the 4-month phenotype, suggests that this temperamental profile may be a fruitful target for high-risk genetic studies.
一个困扰着关注人类发展的学科的核心问题是从出生到成熟的连续性和不连续性的本质。杏仁核在大脑对新奇和情绪的处理中起着核心作用。尽管个体对新奇和情绪刺激的杏仁核反应性存在相当大的可变性,但这些个体差异的起源尚不清楚。四个月大的被称为高反应性(HR)的婴儿在实验室中对特定的陌生视觉、听觉和嗅觉刺激表现出独特的剧烈运动和哭泣模式。低反应性婴儿则表现出互补的模式。在这里,我们证明 HR 婴儿表型可以预测近 20 年后成年人对新面孔的杏仁核反应性更大。可以根据 4 个月大的实验室中进行的单次行为评估来预测成熟时大脑功能的个体差异。这是已知的最早的可以预测成熟时神经活动模式个体差异的人类行为表型。这些源于婴儿期的气质差异可能与理解临床精神障碍易感性和弹性的个体差异有关。高反应性婴儿的男性在杏仁核中对新面孔的反应性特别高,这使他们在成年后与所有其他性别/气质亚组区分开来,这表明他们的杏仁核特别容易被陌生面孔所吸引。这些发现强调了在研究人类气质和焦虑障碍的发育神经生物学时考虑性别的重要性。行为和生物中间表型(或“内表型”)的遗传研究为研究基于临床定义的障碍的表型提供了一个重要的替代方法。由于 HR 表型的特点是对基本的视觉、嗅觉和听觉刺激有特定的反应模式,而且在可以观察到害羞或与陌生人害怕互动等复杂的社会行为之前,它可能比以后生命中观察到的行为特征更接近潜在的神经生物学机制。这种可能性,再加上环境因素对 4 个月大的表型的影响时间较短,表明这种气质特征可能是高风险遗传研究的一个有希望的目标。