Diffusion-weighted MR imaging of acute stroke: correlation with T2-weighted and magnetic susceptibility-enhanced MR

M E Moseley1, J Kucharczyk, J Mintorovitch

  • 1Department of Radiology, University of California, San Francisco 94143.

Insights

Diffusion-weighted MRI detects acute ischemic stroke earlier than T2-weighted MRI. This technique accurately maps brain injury within an hour of middle cerebral artery occlusion, correlating with metabolic changes and pathology.

Area of Science:

  • Neuroimaging
  • Medical Physics
  • Stroke Research

Background:

  • Acute ischemic stroke diagnosis relies on timely and accurate imaging.
  • Conventional T2-weighted MRI often shows delayed detection of ischemic injury.
  • Diffusion-weighted MRI (DW-MRI) shows promise for early stroke detection.

Purpose of the Study:

  • To compare the temporal and anatomic accuracy of DW-MRI and contrast-enhanced T2-weighted MRI in detecting acute ischemic stroke.
  • To evaluate the correlation of early MRI findings with metabolic changes and histopathology.

Main Methods:

  • Unilateral middle cerebral artery occlusion was induced in feline models.
  • Diffusion-weighted MRI and T2-weighted MRI (with and without contrast agent Dy-DTPA-BMA) were performed.
  • MR spectroscopy and postmortem histopathology were used for correlation.

Main Results:

  • DW-MRI detected increased signal intensity in the ischemic territory within 1 hour of occlusion.
  • Contrast-enhanced T2-weighted MRI revealed perfusion deficits within 1 hour, closely matching DW-MRI findings.
  • Non-contrast T2-weighted MRI typically failed to detect injury for 2-3 hours.
  • Early DW-MRI signal changes correlated with metabolic disruptions and histopathological findings.

Conclusions:

  • Diffusion-weighted MRI is superior to conventional T2-weighted MRI for early detection of acute cerebral ischemia.
  • Contrast-enhanced T2-weighted MRI can provide complementary information on perfusion deficits.
  • DW-MRI accurately reflects early pathophysiological changes in acute ischemic stroke.