Department of Psychiatry, Harvard Medical School, Boston, MA, USA.
Department of Psychiatry, Harvard Medical School, Boston, MA, USA; Division of Depression and Anxiety, McLean Hospital, Belmont, MA, USA.
J Psychiatr Res. 2021 Sep;141:325-332. doi: 10.1016/j.jpsychires.2021.07.023. Epub 2021 Jul 14.
Posttraumatic stress disorder (PTSD) is associated with lower gray matter volume (GMV) in brain regions critical for extinction of learned threat. However, relationships among volume, extinction learning, and PTSD symptom development remain unclear. We investigated subcortical brain volumes in regions supporting extinction learning and fear-potentiated startle (FPS) to understand brain-behavior interactions that may impact PTSD symptom development in recently traumatized individuals. Participants (N = 99) completed magnetic resonance imaging and threat conditioning two weeks following trauma exposure as part of a multisite observational study to understand the neuropsychiatric effects of trauma (AURORA Study). Participants completed self-assessments of PTSD (PTSD Checklist for DSM-5; PCL-5), dissociation, and depression symptoms two- and eight-weeks post-trauma. We completed multiple regressions to investigate relationships between FPS during late extinction, GMV, and PTSD symptom development. The interaction between thalamic GMV and FPS during late extinction at two weeks post-trauma predicted PCL-5 scores eight weeks (t (75) = 2.49, β = 0.28, p = 0.015) post-trauma. Higher FPS predicted higher PCL-5 scores in the setting of increased thalamic GMV. Meanwhile, lower FPS also predicted higher PCL-5 scores in the setting of decreased thalamic GMV. Thalamic GMV and FPS interactions also predicted posttraumatic dissociative and depressive symptoms. Amygdala and hippocampus GMV by FPS interactions were not associated with posttraumatic symptom development. Taken together, thalamic GMV and FPS during late extinction interact to contribute to adverse posttraumatic neuropsychiatric outcomes. Multimodal assessments soon after trauma have the potential to distinguish key phenotypes vulnerable to posttraumatic neuropsychiatric outcomes.
创伤后应激障碍(PTSD)与大脑中对习得性威胁的消除至关重要的区域的灰质体积(GMV)降低有关。然而,体积、消除学习和 PTSD 症状发展之间的关系仍不清楚。我们研究了支持消除学习和恐惧增强的起始(FPS)的皮质下脑区的体积,以了解可能影响近期创伤后个体 PTSD 症状发展的大脑-行为相互作用。参与者(N=99)在创伤暴露后两周内完成磁共振成像和威胁条件反射,作为理解创伤神经精神影响的多站点观察性研究的一部分(AURORA 研究)。参与者在创伤后两到八周内完成 PTSD(DSM-5 创伤后检查表;PCL-5)、解离和抑郁症状的自我评估。我们完成了多项回归分析,以研究晚期消除过程中的 FPS、GMV 和 PTSD 症状发展之间的关系。创伤后两周时,丘脑 GMV 与晚期消除过程中的 FPS 之间的相互作用预测了创伤后八周的 PCL-5 评分(t(75)=2.49,β=0.28,p=0.015)。较高的 FPS 预测了丘脑 GMV 增加时 PCL-5 评分较高。同时,较低的 FPS 也预测了丘脑 GMV 减少时 PCL-5 评分较高。丘脑 GMV 和 FPS 相互作用也预测了创伤后分离和抑郁症状。杏仁核和海马 GMV 与 FPS 相互作用与创伤后症状发展无关。总的来说,晚期消除过程中的丘脑 GMV 和 FPS 相互作用导致不良的创伤后神经精神结局。创伤后不久的多模态评估有可能区分易受创伤后神经精神结局影响的关键表型。