Diffusion tensor imaging may help the determination of time at onset in cerebral ischaemia
- PMID: 19684233
- DOI: 10.1136/jnnp.2008.163584
Diffusion tensor imaging may help the determination of time at onset in cerebral ischaemia
Abstract
Background and aims: The apparent diffusion coefficient (ADC) and anisotropy (eg, fractional anisotropy (FA)) of ischaemic tissue evolve over time. A reduction in diffusivity (ie, lambda(2) and lambda(3)) is an important marker for characterising hyperacute-stage infarction, as these parameters may reflect axonal membrane status. The study examines whether transverse diffusivity could be useful in assessing white matter infarcts of various ages.
Methods: Diffusion tensor imaging data from 44 adult patients (34 men, 10 women, aged 46 to 89 years, mean = 70.3) with acute white matter infarction (1-168 h) of the internal capsule were analysed. Relative eigenvalues were calculated as: (lambda(ipsi)-lambda(contra))/lambda(contra). Lesions were classified based on theoretically expected evolution of diffusivity over time as follows: stage I, FA higher than the contralesional region of interest (ROI); stage II, diffusivity lower than the contralesional side for all eigenvalues; stage III, one of two transverse eigenvalues (lambda(2) or lambda(3)) higher than the contralesional ROI.
Results: Stage I infarcts (n = 5) were found primarily within 24 h of the onset of symptoms, with one case found on the third day. Stage II infarcts were found most commonly within 24 h (n = 18), and fewer after 24 h. After the first day, the ratio of stage III infarcts increased significantly. Thus, diffusivity-based classification of white matter infarcts seems to show a chronological trend.
Conclusions: Diffusion anisotropy may be useful for defining the biological tissue clock of white matter infarctions.
Comment in
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Physiological clocks in acute ischaemic stroke: the search continues.J Neurol Neurosurg Psychiatry. 2009 Sep;80(9):941. doi: 10.1136/jnnp.2008.169110. J Neurol Neurosurg Psychiatry. 2009. PMID: 19684229 No abstract available.
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