Brain Dynamics Centre, Westmead Institute for Medical Research, The University of Sydney, Westmead, Australia.
Department of Psychiatry, University of Sydney, Westmead, Australia.
Transl Psychiatry. 2023 Mar 9;13(1):85. doi: 10.1038/s41398-023-02375-9.
At least one-third posttraumatic stress disorder (PTSD) patients do not respond to trauma-focused psychotherapy (TF-psychotherapy), which is the treatment of choice for PTSD. To clarify the change mechanisms that may be associated with treatment response, this study examined changes in neural activations during affective and non-affective processing that occur with improvement of symptoms after TF-psychotherapy. This study assessed PTSD treatment-seeking patients (n = 27) prior to and after TF-psychotherapy using functional magnetic resonance imaging when they completed three tasks: (a) passive viewing of affective faces, (b) cognitive reappraisal of negative images, and (c) non-affective response inhibition. Patients then underwent 9 sessions of TF-psychotherapy, and were assessed on the Clinician-Administered PTSD Scale following treatment. Changes in neural responses in affect and cognitive processing regions-of-interest for each task were correlated with reduction of PTSD severity from pretreatment to posttreatment in the PTSD cohort. Data from 21 healthy controls was used for comparison. Improvement of symptoms in PTSD were associated with increased activation of left anterior insula, reductions in the left hippocampus and right posterior insula during viewing of supraliminally presented affective images, and reduced connectivity between the left hippocampus with the left amygdala and rostral anterior cingulate. Treatment response was also associated with reduced activation in the left dorsolateral prefrontal cortex during reappraisal of negative images. There were no associations between response and activation change during response inhibition. This pattern of findings indicates that improvement of PTSD symptoms following TF-psychotherapy is associated with changes in affective rather than non-affective processes. These findings accord with prevailing models that TF-psychotherapy promotes engagement and mastery of affective stimuli.Clinical Trials Registration: Trial Registration: Prospectively registered at Australian and New Zealand Clinical Trials Registry, ACTRN12612000185864 and ACTRN12609000324213. https://www.anzctr.org.au/Trial/Registration/TrialReview.aspx?id=83857.
至少有三分之一的创伤后应激障碍(PTSD)患者对创伤聚焦心理疗法(TF-psychotherapy)没有反应,这是 PTSD 的首选治疗方法。为了阐明与治疗反应相关的可能变化机制,本研究在接受 TF-psychotherapy 治疗后症状改善时,检查了情感和非情感处理过程中神经激活的变化。本研究在接受 TF-psychotherapy 治疗前后使用功能磁共振成像评估了 27 名寻求 PTSD 治疗的患者(n=27),当他们完成三项任务时:(a)被动观看情感面孔,(b)对负面图像进行认知重评,以及(c)非情感反应抑制。然后,患者接受了 9 次 TF-psychotherapy 治疗,并在治疗后接受了 PTSD 临床医生管理量表的评估。每个任务的情感和认知处理感兴趣区域的神经反应变化与 PTSD 队列从治疗前到治疗后的 PTSD 严重程度降低相关。比较了来自 21 名健康对照者的数据。PTSD 症状的改善与超阈值呈现情感图像时左前岛叶的激活增加、左海马和右后岛叶的减少以及左海马与左杏仁核和前扣带皮质的连接减少有关。治疗反应还与消极图像再评价时左背外侧前额叶皮质的激活减少有关。在反应抑制过程中,反应和激活变化之间没有关联。这些发现表明,TF-psychotherapy 治疗后 PTSD 症状的改善与情感过程而非非情感过程的变化有关。这些发现与普遍的模型一致,即 TF-psychotherapy 促进了对情感刺激的参与和掌握。
前瞻性注册于澳大利亚和新西兰临床试验注册中心,ACTRN12612000185864 和 ACTRN12609000324213。https://www.anzctr.org.au/Trial/Registration/TrialReview.aspx?id=83857。