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ABSTRACT: Background
Posttraumatic Stress Disorder (PTSD) is commonly treated with exposure-based cognitive therapies that are based on the principles of fear acquisition and extinction learning. Elevations in one of the major endocannabinoids (anandamide) either via inhibition of the primary degrading enzyme (fatty acid amide hydrolase; FAAH) or via a genetic variation in the FAAH gene (C385A; rs324420) has resulted in accelerated extinction learning and enhanced extinction recall among healthy adults. These results suggest that targeting FAAH may be a promising therapeutic approach for PTSD. However, these effects have not yet been comprehensively examined in a PTSD population.Methods
The current study examined whether genetic variation in the FAAH gene (CC [n = 49] vs AA/AC [n = 3
SUBMITTER: Crombie KM
PROVIDER: S-EPMC8715233 | biostudies-literature | 2022
REPOSITORIES: biostudies-literature