Exposure-based therapy changes amygdala and hippocampus resting-state functional connectivity in patients with posttraumatic stress disorder
Basolateral amygdala
Orbitofrontal cortex
Exposure therapy
DOI:
10.1002/da.22816
Publication Date:
2018-09-10T12:44:32Z
AUTHORS (12)
ABSTRACT
Recent research suggests that posttraumatic stress disorder (PTSD) is associated with altered amygdala and hippocampal resting-state functional connectivity (rsFC). However, less has examined whether Prolonged Exposure (PE), a first line exposure-based treatment for PTSD, the potential to alter resting state neural networks.A total of 24 patients PTSD 26 matched trauma-exposed healthy controls (TEHCs) underwent magnetic resonance imaging (fMRI) at baseline. were scanned second time after completing 10-session PE in which narrated detailed trauma account (imaginal exposure) confronted reminders (in vivo extinguish trauma-related fear responses. TEHC again following 10-week waiting period. Seed regions interest (ROIs) included centromedial (CMA), basolateral (BLA), hippocampus.Post- versus pretreatment comparisons indicated increased rsFC BLA CMA orbitofrontal cortex (OFC), hippocampus-medial prefrontal (mPFC) among but not participants.Enhanced hippocampus cortical could underlie improved capacity inhibition re-evaluation threat, heightened memory encoding retrieval ability, respectively. These findings encourage further investigation this circuitry as therapeutic target PTSD.
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