Borst Bibian, Jovanovic Tanja, House Stacey L, Bruce Steven E, Harnett Nathaniel G, Roeckner Alyssa R, Ely Timothy D, Lebois Lauren A M, Young Dmitri, Beaudoin Francesca L, An Xinming, Neylan Thomas C, Clifford Gari D, Linnstaedt Sarah D, Germine Laura T, Bollen Kenneth A, Rauch Scott L, Haran John P, Storrow Alan B, Lewandowski Christopher, Musey Paul I, Hendry Phyllis L, Sheikh Sophia, Jones Christopher W, Punches Brittany E, Hudak Lauren A, Pascual Jose L, Seamon Mark J, Datner Elizabeth M, Pearson Claire, Peak David A, Domeier Robert M, Rathlev Niels K, O'Neil Brian J, Sergot Paulina, Sanchez Leon D, Harte Steven E, Koenen Karestan C, Kessler Ronald C, McLean Samuel A, Ressler Kerry J, Stevens Jennifer S, van Rooij Sanne J H
Department of Psychiatry and Behavioral Sciences, Emory University School of Medicine, Atlanta, Georgia; Faculty of Behavioural and Movement Sciences, Vrije Universiteit Amsterdam, Amsterdam, the Netherlands.
Department of Psychiatry and Behavioral Neurosciences, Wayne State University, Detroit, Michigan.
Biol Psychiatry Cogn Neurosci Neuroimaging. 2024 Jul;9(7):668-680. doi: 10.1016/j.bpsc.2024.03.002. Epub 2024 Mar 22.
Females are more likely to develop posttraumatic stress disorder (PTSD) than males. Impaired inhibition has been identified as a mechanism for PTSD development, but studies on potential sex differences in this neurobiological mechanism and how it relates to PTSD severity and progression are relatively rare. Here, we examined sex differences in neural activation during response inhibition and PTSD following recent trauma.
Participants (n = 205, 138 female sex assigned at birth) were recruited from emergency departments within 72 hours of a traumatic event. PTSD symptoms were assessed 2 weeks and 6 months posttrauma. A Go/NoGo task was performed 2 weeks posttrauma in a 3T magnetic resonance imaging scanner to measure neural activity during response inhibition in the ventromedial prefrontal cortex, right inferior frontal gyrus, and bilateral hippocampus. General linear models were used to examine the interaction effect of sex on the relationship between our regions of interest and the whole brain, PTSD symptoms at 6 months, and symptom progression between 2 weeks and 6 months.
Lower response inhibition-related ventromedial prefrontal cortex activation 2 weeks posttrauma predicted more PTSD symptoms at 6 months in females but not in males, while greater response inhibition-related right inferior frontal gyrus activation predicted lower PTSD symptom progression in males but not females. Whole-brain interaction effects were observed in the medial temporal gyrus and left precentral gyrus.
There are sex differences in the relationship between inhibition-related brain activation and PTSD symptom severity and progression. These findings suggest that sex differences should be assessed in future PTSD studies and reveal potential targets for sex-specific interventions.
女性比男性更易患创伤后应激障碍(PTSD)。抑制功能受损已被确定为PTSD发生的一种机制,但关于这种神经生物学机制中潜在的性别差异以及它与PTSD严重程度和病程的关系的研究相对较少。在此,我们研究了近期创伤后反应抑制过程中的神经激活以及PTSD中的性别差异。
在创伤事件发生72小时内从急诊科招募参与者(n = 205,其中138名出生时被指定为女性)。在创伤后2周和6个月评估PTSD症状。创伤后2周在3T磁共振成像扫描仪中进行Go/NoGo任务,以测量腹内侧前额叶皮质、右下额叶回和双侧海马体在反应抑制过程中的神经活动。使用一般线性模型来检验性别对感兴趣区域与全脑之间的关系、6个月时的PTSD症状以及2周和6个月之间症状进展的交互作用。
创伤后2周与反应抑制相关的腹内侧前额叶皮质激活较低,预测女性在6个月时PTSD症状更多,而男性则不然;与反应抑制相关的右下额叶回激活较高,预测男性PTSD症状进展较低,而女性则不然。在内侧颞叶回和左中央前回观察到全脑交互作用。
与抑制相关的大脑激活与PTSD症状严重程度和病程之间的关系存在性别差异。这些发现表明,未来的PTSD研究应评估性别差异,并揭示针对性别特异性干预的潜在靶点。