Noninvasive Detection of Cerebral Hypoperfusion and Reversible Ischemia from Reductions in the Magnetic Resonance Imaging Relaxation Time, T2

Author:

Gröhn Olli H. J.1,Lukkarinen Jouko A.1,Oja Joni M. E.12,van Zijl Peter C. M.2,Ulatowski John A.3,Traystman Richard J.3,Kauppinen Risto A.1

Affiliation:

1. NMR Research Group, A.I. Virtanen Institute, University of Kuopio, Kuopio, Finland

2. Department of Radiology, A.I. Virtanen Institute, University of Kuopio, Kuopio, Finland

3. Anesthesiology and Critical Care Medicine, Johns Hopkins University Medical School, Baltimore, Maryland, U.S.A.

Abstract

The hypothesis was tested that hypoperfused brain regions, such as the ischemic penumbra, are detectable by reductions in absolute transverse relaxation time constant ( T2) using magnetic resonance imaging (MRI). To accomplish this, temporal evolution of T2 was measured in several models of hypoperfusion and focal cerebral ischemia in the rat at 9.4 T. Occurrence of acute ischemia was determined through the absolute diffusion constant Dav = 1/3Trace [double overline] D, while perfusion was assessed by dynamic contrast imaging. Three types of regions at risk of infarction could be distinguished: (1) areas with reduced T2 (4% to 15%, all figures relative to contralateral hemisphere) and normal Dav, corresponding to hypoperfusion without ischemia; (2) areas with both reduced T2 (4% to 12%) and Dav (22% to 49%), corresponding to early hypoperfusion with ischemia; (3) areas with increased T2 (2% to 9%) and reduced Dav (28% to 45%), corresponding to irreversible ischemia. In the first two groups, perfusion-deficient regions detected by bolus tracking were similar to those with initially reduced T2. In the third group, bolus tracking showed barely detectable arrival of the tracer in the region where Dav was reduced. We conclude that T2 reduction in acute ischemia can unambiguously identify regions at risk and potentially discriminate between reversible and irreversible hypoperfusion and ischemia.

Publisher

SAGE Publications

Subject

Cardiology and Cardiovascular Medicine,Clinical Neurology,Neurology

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