Publication

Structural connectivity and risk for anhedonia after trauma: A prospective study and replication

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Last modified
  • 05/22/2025
Type of Material
Authors
    Negar Fani, Emory UniversityVasiliki Michopoulos, Emory UniversitySanne van Rooij, Emory UniversityCherita Clendinen, Emory UniversityRaven A. Hardy, Emory UniversityTanja Jovanovic, Emory UniversityBarbara Rothbaum, Emory UniversityKerry Ressler, Emory UniversityJennifer Stevens, Emory University
Language
  • English
Date
  • 2019-09-01
Publisher
  • PERGAMON-ELSEVIER SCIENCE LTD
Publication Version
Copyright Statement
  • © 2019
License
Final Published Version (URL)
Title of Journal or Parent Work
Volume
  • 116
Start Page
  • 34
End Page
  • 41
Grant/Funding Information
  • This work was primarily supported by National Institute of Mental Health R01 MH094757 (to KJR, BOR), R21 MH106902 (to TJ), U01 MH110925 (to KJR, TJ), K12 HD085850 (to VM), and MH101380 (to NF).
Supplemental Material (URL)
Abstract
  • Anhedonia emerges in some people after psychological trauma, reflected by a loss of interest, diminished affect, and detachment. Structural abnormalities in specific neural pathways at the time of trauma may influence the development of these posttraumatic anhedonia (PTA) symptoms. In this prospective study, we determined whether white matter connectivity at around one month post-trauma predicts PTA and other PTSD symptoms at six months post-trauma. Thirty men and women aged 19–62 were recruited from the emergency department of a Level I trauma center. Participants received diffusion tensor imaging at approximately one month post-trauma and clinical assessments at one and six months post-trauma. Probabilistic tractography was used to examine connectivity of select pathways. A replication sample (N = 57) in an independent, cross-sectional dataset of traumatized women was similarly analyzed. Logistic regression results indicated that, after accounting for early PTSD symptoms (at one month) and other clinical risk factors, the integrity of the uncinate fasciculus (UF) uniquely predicted the presence of PTA at six months post-trauma (Beta = −225.6, p < .05). Together, these factors contributed to 76% of the variance in PTA. Integrity of the UF also predicted re-experiencing PTSD symptoms at six months post-trauma. These results were supported in our replication analyses. Our findings indicate that the integrity of the UF around 1 month post-trauma affects vulnerability for the development of anhedonic PTSD symptoms as well as re-experiencing symptoms. Connectivity of this amygdala-ventromedial prefrontal pathway appears to be a salient predictor of anhedonia, above and beyond clinical risk factors.
Author Notes
  • Corresponding author. Emory University, Department of Psychiatry and Behavioral Sciences, 101 Woodruff Circle, Ste 6007, Atlanta, GA, USA, 30322., nfani@emory.edu (N. Fani).
Keywords
Research Categories
  • Psychology, Clinical
  • Biology, Neuroscience

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