Psychiatry Neuroimaging Laboratory, Department of Psychiatry, Brigham and Women's Hospital, Harvard Medical School, 1249 Boylston St, Boston, MA, 02215, USA.
Department of Psychology, University of Ottawa, Ottawa, Canada.
Brain Imaging Behav. 2018 Jun;12(3):870-881. doi: 10.1007/s11682-017-9744-5.
Mild traumatic brain injuries (mTBIs) are often associated with posttraumatic stress disorder (PTSD). In cases of chronic mTBI, accurate diagnosis can be challenging due to the overlapping symptoms this condition shares with PTSD. Furthermore, mTBIs are heterogeneous and not easily observed using conventional neuroimaging tools, despite the fact that diffuse axonal injuries are the most common injury. Diffusion tensor imaging (DTI) is sensitive to diffuse axonal injuries and is thus more likely to detect mTBIs, especially when analyses account for the inter-individual variability of these injuries. Using a subject-specific approach, we compared fractional anisotropy (FA) abnormalities between groups with a history of mTBI (n = 35), comorbid mTBI and PTSD (mTBI + PTSD; n = 22), and healthy controls (n = 37). We compared all three groups on the number of abnormal FA clusters derived from subject-specific injury profiles (i.e., individual z-score maps) along a common white matter skeleton. The mTBI + PTSD group evinced a greater number of abnormally low FA clusters relative to both the healthy controls and the mTBI group without PTSD (p < .05). Across the groups with a history of mTBI, increased numbers of abnormally low FA clusters were significantly associated with PTSD symptom severity, depression, post-concussion symptoms, and reduced information processing speed (p < .05). These findings highlight the utility of subject-specific microstructural analyses when searching for mTBI-related brain abnormalities, particularly in patients with PTSD. This study also suggests that patients with a history of mTBI and comorbid PTSD, relative to those without PTSD, are at increased risk of FA abnormalities.
轻度创伤性脑损伤(mTBI)常与创伤后应激障碍(PTSD)有关。在慢性 mTBI 的情况下,由于这种情况与 PTSD 共享的重叠症状,准确的诊断可能具有挑战性。此外,mTBI 具有异质性,并且尽管弥漫性轴索损伤是最常见的损伤,但使用常规神经影像学工具不易观察到。弥散张量成像(DTI)对弥漫性轴索损伤敏感,因此更有可能检测到 mTBI,尤其是当分析考虑到这些损伤的个体间变异性时。使用个体特异性方法,我们比较了有 mTBI 病史的组(n=35)、伴有 mTBI 和 PTSD 的共病 mTBI 和 PTSD 组(mTBI+PTSD;n=22)和健康对照组(n=37)之间的部分各向异性(FA)异常。我们比较了所有三组源自个体损伤图谱(即个体 z 分数图)的异常 FA 簇数量,沿着共同的白质骨架。与健康对照组和无 PTSD 的 mTBI 组相比,mTBI+PTSD 组表现出更多数量的异常低 FA 簇(p<.05)。在有 mTBI 病史的组中,异常低 FA 簇数量的增加与 PTSD 症状严重程度、抑郁、脑震荡后症状以及信息处理速度降低显著相关(p<.05)。这些发现强调了在寻找与 mTBI 相关的大脑异常时使用个体特异性微观结构分析的效用,尤其是在 PTSD 患者中。这项研究还表明,与没有 PTSD 的患者相比,有 mTBI 和共病 PTSD 病史的患者更有可能出现 FA 异常。