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Vol. 19, No. 5, 2005   

Free Abstract     Article (Fulltext)     Article (PDF 146 KB)     

Original Paper

What Has Diffusion Imaging in Animals Told Us about Diffusion Imaging in Patients with Ischaemic Stroke?
Carly S. Rivers, Joanna M. Wardlaw

Division of Clinical Neurosciences, Western General Hospital, Edinburgh, UK

Address of Corresponding Author

Cerebrovasc Dis 2005;19:328-336 (DOI: 10.1159/000084691)


 goto top of page Key Words

  • Ischaemic stroke
  • Diffusion-weighted imaging
  • Animal model
  • Histology
  • Systematic review

 goto top of page Abstract

Background and Purpose: In acute ischaemic stroke, the amount (and type) of cellular damage underlying diffusion-weighted imaging (DWI) lesion appearances is unclear.We summarized all information from experimental studies of DWI in focal ischaemia models. Methods: We systematically reviewed all published studies of DWI in focal ischaemic stroke models. We extracted key experimental details to determine correlations between histological features and DWI lesion characteristics. Results: Of 141 potentially eligible papers (including more than 2,817 animals, mostly rats), details of key experimental methods were unfortunately often omitted. Consistent findings amongst high-quality studies with blinded analysis included: neuronal damage persists or progresses despite early DWI lesion 'normalisation'; the apparent diffusion coefficient is not very sensitive to the amount of neuronal damage; the 'brighter' the DWI lesion, the greater the neuronal damage; and the DWI lesion may reflect glial more than neuronal changes. Anaesthesia and fixation techniques may inadvertently affect these findings. Conclusions: The relationship between cellular damage and DWI lesion appearance, particularly recovery patterns in reperfusion experiments, remains imprecise. Key experimental details could be reported more completely and consistently. Potential problems from repeated anaesthetics need to be addressed. Early DWI lesion 'recovery' in acute stroke patients may largely reflect glial rather than neuronal 'recovery'.

Copyright © 2005 S. Karger AG, Basel


 goto top of page Author Contacts

Prof. J.M. Wardlaw
Division of Clinical Neurosciences, Bramwell Dott Building
Western General Hospital, Crewe Road
Edinburgh EH4 2XU (UK)
Tel. +44 131 537 3110, Fax +44 131 332 5150, E-Mail jmw@skull.dcn.ed.ac.uk


 goto top of page Article Information

Received: December 8, 2004
Accepted: January 2, 2005
Published online: March 24, 2005
Number of Print Pages : 9
Number of Figures : 2, Number of Tables : 4, Number of References : 27

 
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