Alterations in cerebral perfusion in posttraumatic stress disorder patients without re-exposure to accident-related stimuli

Clin Neurophysiol. 2006 Mar;117(3):637-42. doi: 10.1016/j.clinph.2005.10.020. Epub 2006 Jan 19.

Abstract

Functional neuroimaging studies have shown abnormalities of limbic regions in patients with posttraumatic stress disorder (PTSD) during symptom provocation and cognitive activation.

Objective: The aim of this study was to determine whether PTSD patients without re-exposure to accident-related stimuli would exhibit alterations in cerebral perfusion compared with age-matched normal subjects.

Methods: Brain perfusion SPECT was measured in medication-free 23 PTSD patients and 64 age-matched healthy subjects under resting conditions and analyzed using statistical parametric mapping to compare between the patient and control groups.

Results: We found that PTSD patients exhibited increased cerebral blood perfusion in limbic regions and decreased perfusion in the superior frontal gyrus and parietal and temporal regions in comparison with those of the normal controls.

Conclusions: This result indicates that PTSD patients have alterations in cerebral perfusion of limbic regions and the frontal and temporal cortex without re-exposure to accident-related stimuli.

Significance: This finding supports the hypothesis of the involvement of limbic regions, which might be associated with the regulation of emotion and memory, in the pathophysiology of PTSD.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Analysis of Variance
  • Brain Mapping
  • Case-Control Studies
  • Cognition / physiology
  • Female
  • Functional Laterality / physiology
  • Humans
  • Image Processing, Computer-Assisted / methods
  • Limbic System / blood supply*
  • Limbic System / diagnostic imaging
  • Male
  • Memory / physiology*
  • Middle Aged
  • Regional Blood Flow
  • Stress Disorders, Post-Traumatic / diagnostic imaging
  • Stress Disorders, Post-Traumatic / physiopathology*
  • Tomography, Emission-Computed, Single-Photon / methods