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早期青少年焦虑唤醒的结构连接组学:转化临床和行为学研究发现。

Structural connectomics of anxious arousal in early adolescence: Translating clinical and ethological findings.

机构信息

University of North Carolina at Chapel Hill, United States.

出版信息

Neuroimage Clin. 2017 Sep 21;16:604-609. doi: 10.1016/j.nicl.2017.09.012. eCollection 2017.

DOI:10.1016/j.nicl.2017.09.012
PMID:28971010
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5619942/
Abstract

Etiological explanations of clinical anxiety can be advanced through understanding the neural mechanisms associated with anxiety in youth prior to the emergence of psychopathology. In this vein, the present study sought to investigate how trait anxiety is related to features of the structural connectome in early adolescence. 40 adolescents (21 female, mean age = 13.49 years) underwent a diffusion-weighted imaging scan. We hypothesized that the strength of several a priori defined structural connections would vary with anxious arousal based on previous work in human clinical neuroscience and adult rodent optogenetics. First, connection strength of caudate to rostral middle frontal gyrus was predicted to be anticorrelated with anxious arousal, predicated on extant work in clinically-diagnosed adolescents. Second, connection strength of amygdala to rostral anterior cingulate and to medial orbital frontal cortex would be positively and negatively correlated with anxious arousal, respectively, predicated on rodent optogenetics showing the former pathway is anxiogenic and the latter is anxiolytic. We also predicted that levels of anxiety would not vary with measures of global network topology, based on reported null findings. Results support that anxiety in early adolescence is associated with (1) the clinical biomarker connecting caudate to frontal cortex, and (2) the anxiogenic pathway connecting amygdala to rostral anterior cingulate, both in left but not right hemisphere. Findings support that in early adolescence, anxious arousal may be related to mechanisms that increase anxiogenesis, and not in a deficit in regulatory mechanisms that support anxiolysis.

摘要

临床焦虑的病因解释可以通过了解青少年出现精神病理学之前与焦虑相关的神经机制来推进。本着这种精神,本研究旨在调查特质焦虑与青少年早期结构连接组特征的关系。40 名青少年(21 名女性,平均年龄 13.49 岁)接受了弥散加权成像扫描。我们假设,根据人类临床神经科学和成年大鼠光遗传学的先前工作,几个预先定义的结构连接的强度将根据焦虑唤醒而变化。首先,基于对临床诊断青少年的研究,预测尾状核到额中回的连接强度与焦虑唤醒呈负相关。其次,杏仁核与前扣带回和内侧眶额皮质的连接强度将分别与焦虑唤醒呈正相关和负相关,基于大鼠光遗传学显示前者是焦虑原性的,后者是抗焦虑的。我们还预测,基于报告的无效发现,焦虑水平不会随整体网络拓扑结构的测量而变化。结果支持青少年早期的焦虑与(1)连接尾状核到额叶的临床生物标志物,以及(2)连接杏仁核到前扣带回的焦虑原性通路有关,这两个通路均在左半球而不在右半球。研究结果支持,在青少年早期,焦虑唤醒可能与增加焦虑原性的机制有关,而不是与支持抗焦虑的调节机制的缺陷有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6cac/5619942/f6488e5bf3d8/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6cac/5619942/2b1039a57112/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6cac/5619942/09f2bb94ae93/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6cac/5619942/f6488e5bf3d8/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6cac/5619942/2b1039a57112/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6cac/5619942/09f2bb94ae93/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6cac/5619942/f6488e5bf3d8/gr2.jpg

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