Department of Psychiatry, Yale University School of Medicine, New Haven, CT, USA.
1] Department of Psychiatry, Yale University School of Medicine, New Haven, CT, USA [2] Department of Neurobiology, Yale University School of Medicine, New Haven, CT, USA [3] Department of Child Study, Yale University School of Medicine, New Haven, CT, USA.
Neuropsychopharmacology. 2014 Feb;39(3):670-80. doi: 10.1038/npp.2013.250. Epub 2013 Sep 20.
Cumulative adversity (CA) increases stress sensitivity and risk of adverse health outcomes. However, neural mechanisms underlying these associations in humans remain unclear. To understand neural responses underlying the link between CA and adverse health symptoms, the current study assessed brain activity during stress and neutral-relaxing states in 75 demographically matched, healthy individuals with high, mid, and low CA (25 in each group), and their health symptoms using the Cornell Medical Index. CA was significantly associated with greater adverse health symptoms (P=0.01) in all participants. Functional magnetic resonance imaging results indicated significant associations between CA scores and increased stress-induced activity in the lateral prefrontal cortex, insula, striatum, right amygdala, hippocampus, and temporal regions in all 75 participants (p<0.05, whole-brain corrected). In addition to these regions, the high vs low CA group comparison revealed decreased stress-induced activity in the medial orbitofrontal cortex (OFC) in the high CA group (p<0.01, whole-brain corrected). Specifically, hypoactive medial OFC and hyperactive right hippocampus responses to stress were each significantly associated with greater adverse health symptoms (p<0.01). Furthermore, an inverse correlation was found between activity in the medial OFC and right hippocampus (p=0.01). These results indicate that high CA sensitizes limbic-striatal responses to acute stress and also identifies an important role for stress-related medial OFC and hippocampus responses in the effects of CA on increasing vulnerability to adverse health consequences.
累积逆境 (CA) 会增加压力敏感性和不良健康结果的风险。然而,人类中这些关联的神经机制仍不清楚。为了了解 CA 与不良健康症状之间联系的神经反应,本研究在 75 名具有高、中、低 CA(每组 25 名)的人口统计学匹配的健康个体中,评估了在应激和中性放松状态下的大脑活动,并使用康奈尔医学指数评估了他们的健康症状。CA 与所有参与者的更多不良健康症状显著相关(P=0.01)。功能磁共振成像结果表明,CA 评分与外侧前额叶皮层、岛叶、纹状体、右侧杏仁核、海马体和颞叶区域在所有 75 名参与者中的应激诱导活动增加之间存在显著关联(p<0.05,全脑校正)。除了这些区域外,高 CA 组与低 CA 组的比较显示,高 CA 组的内侧眶额皮层(OFC)在应激诱导活动减少(p<0.01,全脑校正)。具体而言,内侧 OFC 的应激诱导活动减少和右侧海马体的应激诱导活动增加与更多的不良健康症状显著相关(p<0.01)。此外,还发现内侧 OFC 和右侧海马体之间存在负相关(p=0.01)。这些结果表明,高 CA 使边缘-纹状体对急性应激的反应更加敏感,并确定了应激相关的内侧 OFC 和海马体反应在 CA 对增加不良健康后果易感性的影响中的重要作用。