Department of Psychiatry and Behavioral Sciences, Emory University School of Medicine, Atlanta, Georgia.
Department of Psychiatry and Behavioral Sciences, Emory University School of Medicine, Atlanta, Georgia.
Biol Psychiatry. 2018 Jul 15;84(2):106-115. doi: 10.1016/j.biopsych.2017.09.005. Epub 2017 Sep 20.
Understanding the neurobiological mechanisms that predict posttraumatic stress disorder (PTSD) in recent trauma survivors is important for early interventions. Impaired inhibition of fear or behavioral responses is thought to be central to PTSD symptomatology, but its role in predicting PTSD is unknown. Here we examine whether brain function during response inhibition early after a civilian trauma can predict future PTSD symptoms.
Participants (original sample, n = 27; replication sample, n = 31) were recruited in the emergency department within 24 hours of trauma exposure. PTSD symptoms were assessed in the emergency department and 1, 3, and 6 months posttrauma. A Go/NoGo procedure in a 3T magnetic resonance imaging scanner was used to measure neural correlates of response inhibition 1 to 2 months posttrauma. Elastic net regression was used to define the most optimal model to predict PTSD symptoms at 3 and 6 months among demographic, clinical, and imaging measures.
Less hippocampal activation was a significant predictor in the model predicting PTSD symptoms at 3 months (F = 4.33, p = .01) and 6 months (F = 4.96, p = .01). Other significant predictors in the model were race and pain level in the emergency department (3 months), and race and baseline depression symptoms (6 months). Using these predictors in a linear regression in the replication sample again resulted in significant models (3 months [F = 3.03, p = .05], 6 months [F = 5.74, p = .007]) with hippocampal activation predicting PTSD symptoms at 3 and 6 months.
Decreased inhibition-related hippocampal activation soon after trauma predicted future PTSD symptom severity. This finding may contribute to early identification of at-risk individuals and reveals potential targets for intervention or symptom prevention in the aftermath of trauma.
了解预测近期创伤幸存者创伤后应激障碍 (PTSD) 的神经生物学机制对于早期干预至关重要。人们认为,恐惧或行为反应的抑制受损是 PTSD 症状学的核心,但它在预测 PTSD 中的作用尚不清楚。在这里,我们研究了创伤后早期反应抑制期间的大脑功能是否可以预测未来的 PTSD 症状。
参与者(原始样本,n=27;复制样本,n=31)在创伤暴露后 24 小时内从急诊科招募。在急诊科和创伤后 1、3 和 6 个月评估 PTSD 症状。使用 3T 磁共振成像扫描仪中的 Go/NoGo 程序测量创伤后 1 至 2 个月时反应抑制的神经相关性。弹性网回归用于定义预测 3 个月和 6 个月 PTSD 症状的最佳模型,该模型包括人口统计学、临床和影像学指标。
海马体激活减少是预测 3 个月(F=4.33,p=.01)和 6 个月(F=4.96,p=.01)时 PTSD 症状的模型中的显著预测因子。模型中的其他显著预测因子为种族和急诊科疼痛程度(3 个月)以及种族和基线抑郁症状(6 个月)。在复制样本中,使用这些预测因子进行线性回归再次导致显著模型(3 个月 [F=3.03,p=.05],6 个月 [F=5.74,p=.007]),其中海马体激活预测 3 个月和 6 个月时的 PTSD 症状。
创伤后不久抑制相关的海马体激活减少预测未来 PTSD 症状严重程度。这一发现可能有助于早期识别高危个体,并揭示了创伤后干预或症状预防的潜在目标。