焦虑症的神经影像学。

Modern trends in pharmacopsychiatry Pub Date : 2013-01-01 Epub Date: 2013-09-20 DOI:10.1159/000351938
Mats Fredrikson, Vanda Faria
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引用次数: 21

摘要

本文综述了使用功能磁共振成像(fMRI)、正电子发射断层扫描(PET)和单光子发射计算机断层扫描(SPECT)来评估焦虑障碍患者与情感产生和控制相关的神经功能和神经化学改变的神经影像学研究。我们对症状激发研究进行了荟萃分析,使用功能磁共振成像(fMRI)、PET或SPECT测量神经活动,以验证前额叶区域调节杏仁核活动的假设。数据显示,患有恐惧症和创伤后应激障碍(PTSD)的患者的杏仁核反应性增强。在创伤后应激障碍和恐惧状态下,背前扣带皮层与杏仁核一起被激活,这表明它在恐惧表达中起作用,而不是情绪控制。PTSD和恐惧症患者在症状状态下,腹内侧前额叶皮层包括亚属前扣带皮层和内侧眶额叶皮层的情绪调节区域的活动分别受到抑制。经心理治疗后,杏仁核反应性恢复。包括药理学和心理干预以及安慰剂方案在内的不同治疗方式的治疗效果支持,杏仁核神经活动的减少可能是成功治疗干预的最终共同途径,无论采用何种方法,从而将神经传递与大脑核心恐惧网络关键节点的可塑性联系起来。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Neuroimaging in anxiety disorders.

Neuroimaging studies using functional magnetic resonance imaging (fMRI), positron emission tomography (PET) and single-photon emission computed tomography (SPECT) to evaluate neurofunctional and neurochemical alterations related to the generation and control of affect in patients with anxiety disorders are reviewed. We performed a meta-analysis of symptom provocation studies, where neural activity was measured using fMRI, PET or SPECT to test the hypothesis that prefrontal regions modulate amygdala activity. Data revealed that reactivity in the amygdala was enhanced in patients with phobia as well as posttraumatic stress disorder (PTSD). The dorsal anterior cingulate cortex was activated in concert with the amygdala, both in PTSD and in phobic states, suggesting a role in fear expression, rather than emotional control. Activity in emotion-regulating areas in the ventromedial prefrontal cortex including the subgenual anterior cingulate cortex and the medial orbitofrontal cortex was compromised in the symptomatic state in PTSD and phobic disorders, respectively. Increased amygdala reactivity was restored with psychological treatment. Treatment effects across different modalities including pharmacological and psychological interventions as well as with placebo regimens support that reduction of neural activity in the amygdala may be a final common pathway for successful therapeutic interventions irrespective of method, thereby linking neurotransmission to plasticity in a pivotal node of the core fear network of the brain.

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