Scharfenort R, Menz M, Lonsdorf T B
Department of Systems Neuroscience, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Transl Psychiatry. 2016 Jul 19;6(7):e858. doi: 10.1038/tp.2016.126.
The efficacy of current treatments for anxiety disorders is limited by high relapse rates. Relapse of anxiety disorders and addiction can be triggered by exposure to life adversity, but the underlying mechanisms remain unexplored. Seventy-six healthy adults were a priori selected for the presence or absence of adverse experiences during childhood (CA) and recent past (RA; that is, past 12 months). Participants underwent fear conditioning (day 1) and fear extinction and experimental return-of-fear (ROF) induction through reinstatement (a model for adversity-induced relapse; day 2). Ratings, autonomic (skin conductance response) and neuronal activation measures (functional magnetic resonance imaging (fMRI)) were acquired. Individuals exposed to RA showed a generalized (that is, not CS- specific) fear recall and ROF, whereas unexposed individuals showed differential (that is, CS+ specific) fear recall and ROF on an autonomic level despite no group differences during fear acquisition and extinction learning. These group differences in ROF were accompanied by corresponding activation differences in brain areas known to be involved in fear processing and differentiability/generalization of ROF (that is, hippocampus). In addition, dimensional measures of RA, CA and lifetime adversity were negatively correlated with differential skin conductance responses (SCRs) during ROF and hippocampal activation. As discriminating signals of danger and safety, as well as a tendency for overgeneralization, are core features in clinically anxious populations, these deficits may specifically contribute to relapse risk following exposure to adversity, in particular to recent adversity. Hence, our results may provide first and novel insights into the possible mechanisms mediating enhanced relapse risk following exposure to (recent) adversity, which may guide the development of effective pre- and intervention programs.
当前焦虑症治疗方法的疗效因高复发率而受限。焦虑症和成瘾的复发可能由接触生活逆境引发,但其潜在机制仍未得到探索。76名健康成年人根据童年期(CA)和近期(RA,即过去12个月)是否有不良经历被预先挑选出来。参与者接受了恐惧条件反射训练(第1天),并通过恢复训练进行恐惧消退和实验性恐惧再现(ROF)诱导(一种逆境诱导复发的模型;第2天)。记录了评分、自主神经(皮肤电导反应)和神经元激活指标(功能磁共振成像(fMRI))。暴露于RA的个体表现出全身性(即非特定于条件刺激)的恐惧回忆和ROF,而未暴露个体在自主神经水平上表现出差异性(即特定于条件刺激+)的恐惧回忆和ROF,尽管在恐惧获得和消退学习期间两组没有差异。这些ROF的组间差异伴随着已知参与恐惧处理和ROF的可区分性/泛化(即海马体)的脑区相应的激活差异。此外,RA、CA和终生逆境的维度测量与ROF期间的差异性皮肤电导反应(SCRs)和海马体激活呈负相关。作为危险和安全的辨别信号以及过度泛化的倾向,是临床焦虑人群的核心特征,这些缺陷可能特别导致暴露于逆境尤其是近期逆境后的复发风险。因此,我们的结果可能为接触(近期)逆境后介导复发风险增加的可能机制提供首个新颖的见解,这可能指导有效的预防和干预方案的制定。