Stroke, Vol 25, 843-848, Copyright © 1994 by American Heart Association
CC Hanstock, AI Faden, MR Bendall and R Vink
BACKGROUND AND PURPOSE: Diffusion-weighted magnetic resonance imaging (MRI)
has been shown to be particularly effective in detecting early (0 to 4
hours) pathophysiological changes in localized brain regions after cerebral
ischemia. The present study sought to establish whether diffusion-weighted
MRI would be similarly effective in predicting outcome after traumatic
brain injury. METHODS: Diffusion-weighted MRI images and T2-weighted MRI
images were obtained over 4 hours after either moderate fluid
percussion-induced traumatic brain injury or unilateral carotid ligation in
rats. RESULTS: Diffusion-weighted MRI images of traumatic brain injury
demonstrated focal regions of image hypointensity as early as 1 hour after
trauma. The relative diffusion coefficient in these hypointense regions was
significantly increased (P < .005) by 4 hours after trauma compared with
the noninjured hemisphere, but only in the transverse plane in the x
direction. In contrast, induction of diffuse, nonfocal ischemia by
unilateral carotid ligation resulted in scattered regions of hyperintensity
with a significant (P < .001) decrease in relative diffusion coefficient
as early as 1 hour after ligation compared with the noninjured hemisphere.
This decrease exhibited no directionality. CONCLUSIONS: We conclude that
traumatic brain injury results in an increased water diffusion distance
with the directionality indicative of bulk flow of extracellular fluid
toward the lateral ventricles (vasogenic edema). In contrast, the decreased
water diffusion distance with no apparent directionality observed in
ischemia is most likely indicative of cytotoxic edema. Diffusion-weighted
MRI therefore has the potential to differentiate cases of traumatic brain
injury with no focal ischemia from those instances of traumatic brain
injury in which focal ischemia is a complication.
ARTICLES
Diffusion-weighted imaging differentiates ischemic tissue from traumatized tissue
Department of Molecular Sciences, James Cook University, Townsville, Queensland, Australia.
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