Neural Correlates of Procedural Variants in Cognitive-Behavioral Therapy: A Randomized, Controlled Multicenter fMRI Study

Neural Correlates of Procedural Variants in Cognitive-Behavioral Therapy: A Randomized, Controlled Multicenter fMRI Study
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认知行为治疗中程序变异的神经相关性:一项随机、受控的多中心功能磁共振成像研究

DOI:
10.1159/000359955
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发表时间:
2014
影响因子:
22.8
通讯作者:
Kircher T
Kircher T
中科院分区:
医学1区
文献类型:
--
作者:
Straube B;Lueken U;Jansen A;Konrad C;Gloster AT;Gerlach AL;Ströhle A;Wittmann A;Pfleiderer B;Gauggel S;Wittchen HU;Arolt V;Kircher T

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背景认知行为疗法(CBT)是治疗广场恐怖症(PD/AG)的有效方法。目前尚不清楚CBT的变体如何不同地调节PD/AG中涉及的大脑网络。本研究旨在评估治疗师引导(T+)与自我引导(T-)暴露对PD/AG患者恐惧条件反射神经相关因子的影响。方法在一项随机、对照的多中心临床试验中,对无药物治疗的PD/AG患者进行12次手动CBT治疗,在CBT前(t1)和CBT后(t2)的恐惧调节期间使用功能磁共振成像(fMRI)。获得42例患者和42例健康受试者(HS)的质量控制fMRI数据。患者被随机分配到两种CBT变体(T+, n= 22, T-, n= 20)。结果诊断(PD/AG、HS)、治疗组(T+、T-)、时间点(t1、t2)和刺激类型(条件刺激:有、无)的交互作用显示左侧海马和坐骨颞叶皮层活化。T+组在t2 (t2> t1)海马激活增加,这与治疗结果呈正相关,并且随着时间的推移,左侧额下回与左侧海马之间的连通性下降(t1> t2)。结论在T+暴露后,与后海马相关的事件编码过程被增强,并且与左侧额下回的过程更加分离,而这些过程先前被证明在PD/AG中被功能障碍激活。将单一的程序变异与神经基质联系起来,为有针对性的心理治疗干预措施的优化提供了信息。
BackgroundCognitive behavioral therapy (CBT) is an effective treatment for panic disorder with agoraphobia (PD/AG). It is unknown, how variants of CBT differentially modulate brain networks involved in PD/AG. This study was aimed to evaluate the effects of therapist-guided (T+) versus self-guided (T-) exposure on the neural correlates of fear conditioning in PD/AG.MethodIn a randomized, controlled multicenter clinical trial in medication-free patients with PD/AG who were treated with 12 sessions of manualized CBT, functional magnetic resonance imaging (fMRI) was used during fear conditioning before (t1) and after CBT (t2). Quality-controlled fMRI data from 42 patients and 42 healthy subjects (HS) were obtained. Patients were randomized to two variants of CBT (T+, n= 22, and T-, n= 20).ResultsThe interaction of diagnosis (PD/AG, HS), treatment group (T+, T-), time point (t1, t2) and stimulus type (conditioned stimulus: yes, no) revealed activation in the left hippocampus and the occipitotemporal cortex. The T+ group demonstrated increased activation of the hippocampus at t2 (t2> t1), which was positively correlated with treatment outcome, and a decreased connectivity between the left inferior frontal gyrus and the left hippocampus across time (t1> t2).ConclusionAfter T+ exposure, contingency-encoding processes related to the posterior hippocampus are augmented and more decoupled from processes of the left inferior frontal gyrus, previously shown to be dysfunctionally activated in PD/AG. Linking single procedural variants to neural substrates offers the potential to inform about the optimization of targeted psychotherapeutic interventions.
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