4.3 Article

Right inferior frontal gyrus and ventromedial prefrontal activation during response inhibition is implicated in the development of PTSD symptoms

Journal

EUROPEAN JOURNAL OF PSYCHOTRAUMATOLOGY
Volume 13, Issue 1, Pages -

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1080/20008198.2022.2059993

Keywords

Trauma; posttraumatic stress disorder; reactive inhibition; MRI

Funding

  1. National Center for Complementary and Integrative Health [K23AT009713]
  2. National Institute of Mental Health [K01MH121653, R01 MHR01 MH094757, R21 MH106902, R01 MH117009, R01 MH094757-01]
  3. Center for Advanced Brain Imaging, Georgia State University/Georgia Institute of Technology (CABI)
  4. Brain and Behaviour Research Foundation (National Alliance for Research on Schizophrenia and Depression) Distinguished Investigator Grant
  5. Wounded Warrior Project, Department of Defense Clinical Trial grant [W81XWH-10-1-1045]
  6. McCormick Foundation
  7. Genentech
  8. Jazz Pharmaceuticals
  9. Aptinyx

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This study used functional magnetic resonance imaging (fMRI) to examine the predictive role of impaired reactive and proactive inhibition on the development of PTSD symptoms after acute trauma. The findings suggest that reduced activation in the right inferior frontal gyrus (rIFG) and ventromedial prefrontal cortex (vmPFC) during response inhibition may predict the development of PTSD symptoms six months after trauma exposure.
Background Inhibition is a critical executive control process and an established neurobiological phenotype of PTSD, yet to our knowledge, no prospective studies have examined this using a contextual cue task that enables measurement of behavioural response and neural activation patterns across proactive and reactive inhibition. Objective The current longitudinal study utilised functional magnetic resonance imaging (fMRI) to examine whether deficits in proactive and reactive inhibition predicted PTSD symptoms six months after trauma. Method Twenty-three (65% males) medical patients receiving emergency medical care from a level 1 trauma centre were enrolled in the study and invited for an MRI scan 1-2-months post-trauma. PTSD symptoms were measured using self-report at scan and 6-months post-trauma. A stop-signal anticipation task (SSAT) during an fMRI scan was used to test whether impaired behavioural proactive and reactive inhibition, and reduced activation in right inferior frontal gyrus (rIFG), ventromedial prefrontal cortex (vmPFC), and bilateral hippocampus, were related to PTSD symptoms. We predicted that lower activation levels of vmPFC and rIFG during reactive inhibition and lower activation of hippocampus and rIFG during proactive inhibition would relate to higher 6-month PTSD symptoms. Results No significant associations were found between behavioural measures and 6-month PTSD. Separate linear regression analyses showed that reduced rIFG activation (F-1,F-21 = 9.97, R-2 = .32, p = .005) and reduced vmPFC activation (F-1,F-21 = 5.19, R-2 = .20, p = .03) significantly predicted greater 6-month PTSD symptoms; this result held for rIFG activation controlling for demographic variables and baseline PTSD symptoms (beta = -.45, p = .04) and Bonferroni correction. Conclusion Our findings suggest that impaired rIFG and, to a lesser extent, vmPFC activation during response inhibition may predict the development of PTSD symptoms following acute trauma exposure. Given the small sample size, future replication studies are needed.

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