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Evolution of hyperacute stroke over 6 hours using serial MR perfusion and diffusion maps
Purpose To develop an appropriate method to evaluate the time‐course of diffusion and perfusion changes in a clinically relevant animal model of ischemic stroke and to examine lesion progression on MR images. An exploration of acute stroke infarct expansion was performed in this study by using a new...
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Published in: | Journal of magnetic resonance imaging 2009-06, Vol.29 (6), p.1262-1270 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Purpose
To develop an appropriate method to evaluate the time‐course of diffusion and perfusion changes in a clinically relevant animal model of ischemic stroke and to examine lesion progression on MR images. An exploration of acute stroke infarct expansion was performed in this study by using a new methodology for developing time‐to‐infarct maps based on the time at which each voxel becomes infarcted. This enabled definition of homogeneous regions from the heterogeneous stroke infarct.
Materials and Methods
Time‐to‐infarct maps were developed based on apparent diffusion coefficient (ADC) changes. These maps were validated and then applied to blood flow and time‐to‐peak maps to examine perfusion changes.
Results
ADC stroke infarct showed different evolution patterns depending on the time at which that region of tissue infarcted. Applying the time‐to‐infarct maps to the perfusion maps showed localized perfusion evolution characteristics. In some regions, perfusion was immediately affected and showed little change over the experiment; however, in some regions perfusion changes were more dynamic.
Conclusion
Results were consistent with the diffusion‐perfusion mismatch hypothesis. In addition, characteristics of collateral recruitment were identified, which has interesting stroke pathophysiology and treatment implications. J. Magn. Reson. Imaging 2009;29:1262–1270. © 2009 Wiley‐Liss, Inc. |
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ISSN: | 1053-1807 1522-2586 |
DOI: | 10.1002/jmri.21763 |