Perfusion MR Imaging Using a 3D Pulsed Continuous Arterial Spin-Labeling Method for Acute Cerebral Infarction

Y Shinohara1, A Kato2, K Kuya2

  • 1From the Division of Radiology (Y.S., A.K., K.K., T.O.), Department of Pathophysiological and Therapeutic Science, Faculty of Medicine shino-y@olive.plala.or.jp.

Insights

3D arterial spin-labeling detects crossed cerebellar diaschisis in branch atheromatous disease, a stroke subtype. This imaging biomarker correlates with neurologic severity, aiding in stroke outcome prediction.

Area of Science:

  • Neurology
  • Radiology
  • Medical Imaging

Background:

  • Branch atheromatous disease is a stroke subtype associated with early neurologic deterioration.
  • Crossed cerebellar diaschisis is influenced by supratentorial perfusion abnormalities and impacts ischemic stroke outcomes.

Purpose of the Study:

  • To evaluate the utility of whole-brain 3D pulsed continuous arterial spin-labeling (ASL) as an imaging biomarker.
  • To predict neurologic severity in patients with branch atheromatous disease.

Main Methods:

  • Twenty-three patients with branch atheromatous disease underwent MR imaging, including DWI, 3D-TOF-MRA, and 3D-ASL.
  • Measured asymmetry indices of cerebral blood flow (CBF) in the affected area and contralateral cerebellum (crossed cerebellar diaschisis).
  • Correlated these parameters and DWI infarct volume with the initial National Institutes of Health Stroke Scale (NIHSS) score.

Main Results:

  • No correlation was found between NIHSS score and CBF asymmetry in the affected area (r = -0.027, P = .724).
  • Significant correlations were observed between NIHSS score and crossed cerebellar diaschisis (r = 0.515, P = .012).
  • DWI infarct volume also showed a significant correlation with NIHSS score (r = 0.664, P = .001).

Conclusions:

  • 3D-arterial spin-labeling can effectively detect crossed cerebellar diaschisis in branch atheromatous disease.
  • Crossed cerebellar diaschisis detected by 3D-ASL is a significant imaging biomarker correlated with neurologic severity.
Abstract