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首页> 外文期刊>Biological psychiatry >The Role of the Hippocampus in Predicting Future Posttraumatic Stress Disorder Symptoms in Recently Traumatized Civilians
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The Role of the Hippocampus in Predicting Future Posttraumatic Stress Disorder Symptoms in Recently Traumatized Civilians

机译:海马的作用在最近创伤平民预测未来失败的宫外应激障碍症状

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BackgroundUnderstanding 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. MethodsParticipants (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. ResultsLess hippocampal activation was a significant predictor in the model predicting PTSD symptoms at 3 months (F11,22?= 4.33,p?= .01) and 6 months (F9,19?= 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 [F3,23?= 3.03,p?=.05], 6 months [F3,20?= 5.74,p?=.007]) with hippocampal activation predicting PTSD symptoms at 3 and 6 months. ConclusionsDecreased 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.
机译:背景技术预测最近的创伤幸存者在最近的创伤幸存者(PTSD)的神经生物学机制对于早期干预措施是重要的。抑制恐惧或行为反应的抑制受损被认为是可行的症状症状,但其在预测PTSD中的作用是未知的。在这里,我们在平民创伤后早期抑制脑功能是否可以预测未来的应激症状。在创伤暴露的24小时内,在急诊部门招募了方法颗粒(原始样品,N = 27;复制样品,N?= 31)。在急诊部门和1,3和6个月内评估了PTSD症状。 3T磁共振成像扫描仪中的GO / NOGO过程用于测量后抑制1至2个月的神经相关性。弹性净回归用于定义最佳的模型,以预测人口统计,临床,临床和成像措施的3个月和6个月。没有结果海马活化是在3个月内预测PTSD症状的模型中的显着预测因子(F11,22?= 4.33,p?= .01)和6个月(F9,19?= 4.96,p?= .01)。该模型中的其他重要预测因子是急诊部(3个月)的种族和疼痛水平,种族和基准抑郁症状(6个月)。在复制样品中的线性回归中使用这些预测器再次导致显着模型(3个月[F3,23吗?= 3.03,P?=。05],6个月[F3,20吗?5.74,P?=。007] )海马激活预测3个月和6个月的症状。结论在创伤预测未来PTSD症状严重程度后不久的抑制相关的海马活化。这一发现可能有助于早期识别风险,并揭示创伤后的干预或症状预防潜在目标。

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