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1.
Acta Psychiatr Scand ; 138(4): 312-324, 2018 10.
Article in English | MEDLINE | ID: mdl-29952088

ABSTRACT

OBJECTIVE: Exposure to sexual assault is a significant risk factor to develop post-traumatic stress disorder (PTSD) in females. The early neurobiological changes leading to the development of PTSD remain understudied and unclear in this population. METHODS: Participants were 27 adult females recruited within a month following exposure to sexual assault (T1) and 20 age-matched non-exposed controls. Among the victims, 10 participants met (PTSD+) and 15 did not meet (PTSD-) DSM-IV criteria for PTSD 6 months post-trauma (T2). At both visits, hippocampal and amygdala volumes were extracted from magnetic resonance imaging scans, and indices of total diurnal cortisol changes were derived from individual areas under the curve relative to the ground (AUCg). Measures at T1 were compared between groups at T1, measures at T2 between groups at T2, and measures at T1 between groups at T2. RESULTS: At T1, victims had significantly smaller bilateral hippocampal volumes, but not AUCg, than controls. At T2, neither hippocampal volume nor AUCg significantly differed among the groups. However, the PTSD+ group had significantly smaller hippocampal volumes at T1 than the control group, but not compared to the PTSD- group. CONCLUSIONS: This study indicates that having smaller hippocampal volumes is a risk factor to develop PTSD in females exposed to sexual assault.


Subject(s)
Hippocampus/pathology , Sex Offenses , Stress Disorders, Post-Traumatic/pathology , Adolescent , Adult , Amygdala/diagnostic imaging , Amygdala/pathology , Female , Follow-Up Studies , Hippocampus/diagnostic imaging , Humans , Magnetic Resonance Imaging , Middle Aged , Risk Factors , Stress Disorders, Post-Traumatic/diagnostic imaging , Stress Disorders, Post-Traumatic/metabolism , Stress Disorders, Post-Traumatic/physiopathology , Young Adult
2.
Psychol Med ; 48(9): 1454-1463, 2018 07.
Article in English | MEDLINE | ID: mdl-28994360

ABSTRACT

BACKGROUND: Childhood trauma is a risk factor for psychosis. Deficits in response inhibition are common to psychosis and trauma-exposed populations, and associated brain functions may be affected by trauma exposure in psychotic disorders. We aimed to identify the influence of trauma-exposure on brain activation and functional connectivity during a response inhibition task. METHODS: We used functional magnetic resonance imaging to examine brain function within regions-of-interest [left and right inferior frontal gyrus (IFG), right dorsolateral prefrontal cortex, right supplementary motor area, right inferior parietal lobule and dorsal anterior cingulate cortex], during the performance of a Go/No-Go Flanker task, in 112 clinical cases with psychotic disorders and 53 healthy controls (HCs). Among the participants, 71 clinical cases and 21 HCs reported significant levels of childhood trauma exposure, while 41 clinical cases and 32 HCs did not. RESULTS: In the absence of effects on response inhibition performance, childhood trauma exposure was associated with increased activation in the left IFG, and increased connectivity between the left IFG seed region and the cerebellum and calcarine sulcus, in both cases and healthy individuals. There was no main effect of psychosis, and no trauma-by-psychosis interaction for any other region-of-interest. Within the clinical sample, the effects of trauma-exposure on the left IFG activation were mediated by symptom severity. CONCLUSIONS: Trauma-related increases in activation of the left IFG were not associated with performance differences, or dependent on clinical diagnostic status; increased IFG functionality may represent a compensatory (overactivation) mechanism required to exert adequate inhibitory control of the motor response.


Subject(s)
Child Abuse/psychology , Magnetic Resonance Imaging , Prefrontal Cortex/physiopathology , Psychotic Disorders/physiopathology , Adult , Brain Mapping , Case-Control Studies , Child , Female , Functional Laterality , Humans , Male , Middle Aged , Neural Pathways/physiopathology , Neuropsychological Tests
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