Neuroscience & Public Policy Program, University of Wisconsin-Madison, Madison, WI, USA; Neuroscience Training Program, University of Wisconsin-Madison, Madison, WI, USA; Department of Psychiatry, BRAVE Youth Lab, 6001 Research Park Blvd., Madison, WI 53719, USA.
Neuroscience Training Program, University of Wisconsin-Madison, Madison, WI, USA; Department of Psychiatry, BRAVE Youth Lab, 6001 Research Park Blvd., Madison, WI 53719, USA.
Neuroimage Clin. 2019;24:102028. doi: 10.1016/j.nicl.2019.102028. Epub 2019 Oct 21.
Previous studies have identified structural brain abnormalities in pediatric PTSD. However, little is known about what structural brain substrates may confer recovery versus persistence of PTSD in the context of the developing brain.
This naturalistic longitudinal study used T1-weighted MRI to evaluate cortical thickness and surface area in youth with a PTSD diagnosis (n = 28) and typically developing healthy youth (TD; n = 27) at baseline and one-year follow-up. Of the PTSD group, 10 youth were remitters at one-year follow up while 18 had persistent PTSD. Whole-brain estimates of cortical thickness and surface area were extracted to identify differences in cortical architecture associated with PTSD remission and persistence as compared to typical development.
Youth who achieved PTSD remission entered the study with significantly lower trauma exposure and reduced symptom severity as compared to nonremitters. PTSD persistence was associated with decreased surface area over time in the ventrolateral prefrontal cortex (vlPFC) as compared to both remitters and TD youth. In contrast, PTSD remission was associated with expansion of frontal pole surface area and ventromedial PFC (vmPFC) thickness over time. Across clinical groups, vmPFC thickness was further inversely associated with symptom severity.
To our knowledge, these findings represent the first report of cortical substrates underlying persistence versus remission in pediatric PTSD. Together, these findings suggest active structural developmental processes unique to both remission and nonremission in youth with PTSD. In particular, expansion of prefrontal regions implicated in emotion regulation may facilitate recovery from PTSD in youth and would warrant further study.
先前的研究已经确定了儿科 PTSD 患者的大脑结构异常。然而,在发育中的大脑背景下,对于哪些大脑结构基础可能导致 PTSD 的恢复或持续存在,人们知之甚少。
这项自然主义的纵向研究使用 T1 加权 MRI 评估了 PTSD 诊断(n=28)和典型发育健康青少年(TD;n=27)在基线和一年随访时的皮质厚度和表面积。在 PTSD 组中,有 10 名青少年在一年随访时达到缓解,而 18 名青少年持续患有 PTSD。提取全脑皮质厚度和表面积的估计值,以确定与 PTSD 缓解和持续相关的皮质结构差异。
与非缓解者相比,达到 PTSD 缓解的青少年在进入研究时创伤暴露明显减少,症状严重程度降低。与缓解者和 TD 青少年相比,随着时间的推移,PTSD 持续存在与腹外侧前额叶皮层(vlPFC)的表面积减少有关。相比之下,随着时间的推移,PTSD 缓解与额叶极表面积和腹内侧前额叶皮层(vmPFC)厚度的扩张有关。在整个临床组中,vmPFC 厚度与症状严重程度呈负相关。
据我们所知,这些发现代表了儿科 PTSD 中持续存在与缓解的皮质基础的首次报告。总的来说,这些发现表明,PTSD 青少年的缓解和非缓解具有独特的积极的结构发育过程。特别是,涉及情绪调节的前额叶区域的扩张可能有助于青少年 PTSD 的恢复,这值得进一步研究。