Assessment of ischemic penumbra in patients with hyperacute stroke using amide proton transfer (APT) chemical exchange saturation transfer (CEST) MRI. (28th November 2013)
- Record Type:
- Journal Article
- Title:
- Assessment of ischemic penumbra in patients with hyperacute stroke using amide proton transfer (APT) chemical exchange saturation transfer (CEST) MRI. (28th November 2013)
- Main Title:
- Assessment of ischemic penumbra in patients with hyperacute stroke using amide proton transfer (APT) chemical exchange saturation transfer (CEST) MRI
- Authors:
- Tietze, Anna
Blicher, Jakob
Mikkelsen, Irene Klærke
Østergaard, Leif
Strother, Megan K.
Smith, Seth A.
Donahue, Manus J. - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Chemical exchange saturation transfer (CEST)‐derived, pH‐weighted, amide proton transfer (APT) MRI has shown promise in animal studies for the prediction of infarction risk in ischemic tissue. Here, APT MRI was translated to patients with acute stroke (1–24 h post‐symptom onset), and assessments of APT contrast, perfusion, diffusion, disability and final infarct volume (23–92 days post‐stroke) are reported. Healthy volunteers (<italic>n</italic> = 5) and patients (<italic>n</italic> = 10) with acute onset of symptoms (0–4 h, <italic>n</italic> = 7; uncertain onset &lt;24 h, <italic>n</italic> = 3) were scanned with diffusion‐ and perfusion‐weighted MRI, fluid‐attenuated inversion recovery (FLAIR) and CEST. Traditional asymmetry and a Lorentzian‐based APT index were calculated in the infarct core, at‐risk tissue (time‐to‐peak, TTP; lengthening) and final infarct volume. On average (mean ± standard deviation), control white matter APT values (asymmetry, 0.019 ± 0.005; Lorentzian, 0.045 ± 0.006) were not significantly different (<italic>p</italic> &gt; 0.05) from APT values in normal‐appearing white matter (NAWM) of patients (asymmetry, 0.022 ± 0.003; Lorentzian, 0.048 ± 0.003); however, ischemic regions in patients showed reduced (<italic>p</italic> = 0.03) APT effects compared with NAWM. Representative cases are presented, whereby the APT contrast is compared quantitatively with contrast<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Chemical exchange saturation transfer (CEST)‐derived, pH‐weighted, amide proton transfer (APT) MRI has shown promise in animal studies for the prediction of infarction risk in ischemic tissue. Here, APT MRI was translated to patients with acute stroke (1–24 h post‐symptom onset), and assessments of APT contrast, perfusion, diffusion, disability and final infarct volume (23–92 days post‐stroke) are reported. Healthy volunteers (<italic>n</italic> = 5) and patients (<italic>n</italic> = 10) with acute onset of symptoms (0–4 h, <italic>n</italic> = 7; uncertain onset &lt;24 h, <italic>n</italic> = 3) were scanned with diffusion‐ and perfusion‐weighted MRI, fluid‐attenuated inversion recovery (FLAIR) and CEST. Traditional asymmetry and a Lorentzian‐based APT index were calculated in the infarct core, at‐risk tissue (time‐to‐peak, TTP; lengthening) and final infarct volume. On average (mean ± standard deviation), control white matter APT values (asymmetry, 0.019 ± 0.005; Lorentzian, 0.045 ± 0.006) were not significantly different (<italic>p</italic> &gt; 0.05) from APT values in normal‐appearing white matter (NAWM) of patients (asymmetry, 0.022 ± 0.003; Lorentzian, 0.048 ± 0.003); however, ischemic regions in patients showed reduced (<italic>p</italic> = 0.03) APT effects compared with NAWM. Representative cases are presented, whereby the APT contrast is compared quantitatively with contrast from other imaging modalities. The findings vary between patients; in some patients, a trend for a reduction in the APT signal in the final infarct region compared with at‐risk tissue was observed, consistent with tissue acidosis. However, in other patients, no relationship was observed in the infarct core and final infarct volume. Larger clinical studies, in combination with focused efforts on sequence development at clinically available field strengths (e.g. 3.0 T), are necessary to fully understand the potential of APT imaging for guiding the hyperacute management of patients. Copyright © 2013 John Wiley &amp; Sons, Ltd.</p> </abstract> … (more)
- Is Part Of:
- NMR in biomedicine. Volume 27:Number 2(2014:Feb.)
- Journal:
- NMR in biomedicine
- Issue:
- Volume 27:Number 2(2014:Feb.)
- Issue Display:
- Volume 27, Issue 2 (2014)
- Year:
- 2014
- Volume:
- 27
- Issue:
- 2
- Issue Sort Value:
- 2014-0027-0002-0000
- Page Start:
- 163
- Page End:
- 174
- Publication Date:
- 2013-11-28
- Subjects:
- Nuclear magnetic resonance -- Periodicals
Magnetic Resonance Spectroscopy -- Periodicals
574 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/nbm.3048 ↗
- Languages:
- English
- ISSNs:
- 0952-3480
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6113.931000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3033.xml