Anterior hippocampal dysconnectivity in posttraumatic stress disorder: a dimensional and multimodal approach

• Published in: Translational psychiatry Vol. 7; no. 2; p. e1045
• Main Authors: Abdallah, C G, Wrocklage, K M, Averill, C L, Akiki, T, Schweinsburg, B, Roy, A, Martini, B, Southwick, S M, Krystal, J H, Scott, J C
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 28-02-2017; Nature Publishing Group
• Subjects: 692/53/2421; 692/699/476/1414; Adult; Behavioral Sciences; Biological Psychology; Brain - diagnostic imaging; Brain - pathology; Brain - physiopathology; Depression - diagnostic imaging; Depression - physiopathology; Diffusion Magnetic Resonance Imaging; Female; Functional Neuroimaging; Hippocampus - diagnostic imaging; Hippocampus - pathology; Hippocampus - physiopathology; Humans; Magnetic Resonance Imaging; Male; Medicine; Medicine & Public Health; Neurosciences; Organ Size; Original; original-article; Pharmacotherapy; Prefrontal Cortex - diagnostic imaging; Prefrontal Cortex - pathology; Prefrontal Cortex - physiopathology; Psychiatry; Psychological Trauma - diagnostic imaging; Psychological Trauma - physiopathology; Stress Disorders, Post-Traumatic - diagnostic imaging; Stress Disorders, Post-Traumatic - physiopathology; Veterans; War Exposure
• ISSN: 2158-3188; 2158-3188
• DOI: 10.1038/tp.2017.12

The anterior hippocampus (aHPC) has a central role in the regulation of anxiety-related behavior, stress response, emotional memory and fear. However, little is known about the presence and extent of aHPC abnormalities in posttraumatic stress disorder (PTSD). In this study, we used a multimodal approach, along with graph-based measures of global brain connectivity (GBC) termed functional GBC with global signal regression (
f
-GBCr) and diffusion GBC (
d
-GBC), in combat-exposed US Veterans with and without PTSD. Seed-based aHPC anatomical connectivity analyses were also performed. A whole-brain voxel-wise data-driven investigation revealed a significant association between elevated PTSD symptoms and reduced medial temporal
f
-GBCr, particularly in the aHPC. Similarly, aHPC
d
-GBC negatively correlated with PTSD severity. Both functional and anatomical aHPC dysconnectivity measures remained significant after controlling for hippocampal volume, age, gender, intelligence, education, combat severity, depression, anxiety, medication status, traumatic brain injury and alcohol/substance comorbidities. Depression-like PTSD dimensions were associated with reduced connectivity in the ventromedial and dorsolateral prefrontal cortex. In contrast, hyperarousal symptoms were positively correlated with ventromedial and dorsolateral prefrontal connectivity. We believe the findings provide first evidence of functional and anatomical dysconnectivity in the aHPC of veterans with high PTSD symptomatology. The data support the putative utility of aHPC connectivity as a measure of overall PTSD severity. Moreover, prefrontal global connectivity may be of clinical value as a brain biomarker to potentially distinguish between PTSD subgroups.