Clinical Psychology and Neuropsychology, Department of Psychology, University of Konstanz, Germany.
J Psychiatry Neurosci. 2011 May;36(3):176-86. doi: 10.1503/jpn.100010.
So far, the neural network associated with posttraumatic stress disorder (PTSD) has been suggested to mainly involve the amygdala, hippocampus and medial prefrontal cortex. However, increasing evidence indicates that cortical regions extending beyond this network might also be implicated in the pathophysiology of PTSD. We aimed to investigate PTSD-related structural alterations in some of these regions.
We enrolled highly traumatized refugees with and without (traumatized controls) PTSD and nontraumatized controls in the study. To increase the validity of our results, we combined an automatic cortical parcellation technique and voxel-based morphometry.
In all, 39 refugees (20 with and 19 without PTSD) and 13 controls participated in the study. Participants were middle-aged men who were free of psychoactive substances and consumed little to no alcohol. Patients with PTSD (and to a lesser extent traumatized controls) showed reduced volumes in the right inferior parietal cortex, the left rostral middle frontal cortex, the bilateral lateral orbitofrontal cortex and the bilateral isthmus of the cingulate. An influence of cumulative traumatic stress on the isthmus of the cingulate and the lateral orbitofrontal cortex indicated that, at least in these regions, structural alterations might be associated with repeated stress experiences. Voxel-based morphometry analyses produced largely consistent results, but because of a poorer signal-to-noise ratio, conventional statistics did not reach significance.
Although we controlled for several important confounding variables (e.g., sex, alcohol abuse) with our particular sample, this might limit the generalizibility of our data. Moreover, high comorbidity of PTSD and major depression hinders a definite separation of these conditions in our findings. Finally, the results concerning the lateral orbito frontal cortex should be interpreted with caution, as magnetic resonance imaging acquisition in this region is affected by a general signal loss.
Our results indicate that lateral prefrontal, parietal and posterior midline structures are implicated in the pathophysiology of PTSD. As these regions are particularly involved in episodic memory, emotional processing and executive control, this might have important implications for the understanding of PTSD symptoms.
到目前为止,与创伤后应激障碍(PTSD)相关的神经网络主要涉及杏仁核、海马体和内侧前额叶皮质。然而,越来越多的证据表明,该网络之外的皮质区域也可能与 PTSD 的病理生理学有关。我们旨在研究这些区域中与 PTSD 相关的结构改变。
我们招募了患有 PTSD(创伤后应激障碍)和无 PTSD(创伤后应激障碍)的高度创伤难民以及未受创伤的对照者参与研究。为了提高研究结果的有效性,我们结合了自动皮质分割技术和基于体素的形态测量学。
共有 39 名难民(20 名患有 PTSD,19 名无 PTSD)和 13 名对照者参与了研究。参与者均为中年男性,无精神活性物质,酒精摄入极少。患有 PTSD 的患者(以及程度较轻的创伤后应激障碍对照组)表现出右侧顶下小叶、左侧额中回、双侧外侧眶额皮质和双侧扣带回峡部的体积减少。对扣带回峡部和外侧眶额皮质的累积创伤应激的影响表明,至少在这些区域,结构改变可能与反复的应激体验有关。基于体素的形态测量学分析产生了大致一致的结果,但由于信噪比较差,常规统计学未达到显著水平。
尽管我们用特定的样本控制了几个重要的混杂变量(例如,性别、酒精滥用),但这可能限制了我们数据的普遍性。此外,PTSD 和重度抑郁症的高共病性阻碍了我们的研究结果对这些病症的明确区分。最后,应谨慎解释关于外侧眶额皮质的结果,因为该区域的磁共振成像采集受到普遍信号损失的影响。
我们的结果表明,外侧前额叶、顶叶和后中线结构与 PTSD 的病理生理学有关。由于这些区域特别参与情景记忆、情绪处理和执行控制,这可能对理解 PTSD 症状具有重要意义。