Bibian Borst , Tanja Jovanovic , Stacey L. House , Steven E. Bruce , Nathaniel G. Harnett , Alyssa R. Roeckner , Timothy D. Ely , Lauren A.M. Lebois , Dmitri Young , Francesca L. Beaudoin , Xinming An , Thomas C. Neylan , Gari D. Clifford , Sarah D. Linnstaedt , Laura T. Germine , Kenneth A. Bollen , Scott L. Rauch , John P. Haran , Alan B. Storrow , Christopher Lewandowski , Sanne J.H. van Rooij
{"title":"最近遭受创伤的平民中与反应抑制相关的创伤后应激障碍神经预测因子的性别差异。","authors":"Bibian Borst , Tanja Jovanovic , Stacey L. House , Steven E. Bruce , Nathaniel G. Harnett , Alyssa R. Roeckner , Timothy D. Ely , Lauren A.M. Lebois , Dmitri Young , Francesca L. Beaudoin , Xinming An , Thomas C. Neylan , Gari D. Clifford , Sarah D. Linnstaedt , Laura T. Germine , Kenneth A. Bollen , Scott L. Rauch , John P. Haran , Alan B. Storrow , Christopher Lewandowski , Sanne J.H. van Rooij","doi":"10.1016/j.bpsc.2024.03.002","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><p>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.</p></div><div><h3>Methods</h3><p>Participants (<em>n</em> = 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.</p></div><div><h3>Results</h3><p>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.</p></div><div><h3>Conclusions</h3><p>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.</p></div>","PeriodicalId":54231,"journal":{"name":"Biological Psychiatry-Cognitive Neuroscience and Neuroimaging","volume":"9 7","pages":"Pages 668-680"},"PeriodicalIF":5.7000,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Sex Differences in Response Inhibition–Related Neural Predictors of Posttraumatic Stress Disorder in Civilians With Recent Trauma\",\"authors\":\"Bibian Borst , Tanja Jovanovic , Stacey L. House , Steven E. Bruce , Nathaniel G. Harnett , Alyssa R. Roeckner , Timothy D. Ely , Lauren A.M. Lebois , Dmitri Young , Francesca L. Beaudoin , Xinming An , Thomas C. Neylan , Gari D. Clifford , Sarah D. Linnstaedt , Laura T. Germine , Kenneth A. Bollen , Scott L. Rauch , John P. Haran , Alan B. Storrow , Christopher Lewandowski , Sanne J.H. van Rooij\",\"doi\":\"10.1016/j.bpsc.2024.03.002\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><p>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.</p></div><div><h3>Methods</h3><p>Participants (<em>n</em> = 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.</p></div><div><h3>Results</h3><p>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.</p></div><div><h3>Conclusions</h3><p>There are sex differences in the relationship between inhibition-related brain activation and PTSD symptom severity and progression. 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Sex Differences in Response Inhibition–Related Neural Predictors of Posttraumatic Stress Disorder in Civilians With Recent Trauma
Background
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.
Methods
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.
Results
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.
Conclusions
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.
期刊介绍:
Biological Psychiatry: Cognitive Neuroscience and Neuroimaging is an official journal of the Society for Biological Psychiatry, whose purpose is to promote excellence in scientific research and education in fields that investigate the nature, causes, mechanisms, and treatments of disorders of thought, emotion, or behavior. In accord with this mission, this peer-reviewed, rapid-publication, international journal focuses on studies using the tools and constructs of cognitive neuroscience, including the full range of non-invasive neuroimaging and human extra- and intracranial physiological recording methodologies. It publishes both basic and clinical studies, including those that incorporate genetic data, pharmacological challenges, and computational modeling approaches. The journal publishes novel results of original research which represent an important new lead or significant impact on the field. Reviews and commentaries that focus on topics of current research and interest are also encouraged.