4.5 Article

Quantitative chemical exchange saturation transfer imaging of nuclear overhauser effects in acute ischemic stroke

期刊

MAGNETIC RESONANCE IN MEDICINE
卷 88, 期 1, 页码 341-356

出版社

WILEY
DOI: 10.1002/mrm.29187

关键词

acute ischemic stroke; chemical exchange saturation transfer; nuclear Overhauser effect

资金

  1. Cancer Research UK [C5255/A15935]
  2. Dunhill Medical Trust [OSRP1/1006]
  3. Engineering and Physical Sciences Research Council [EP/G036861/1]
  4. National Institute for Health Research
  5. Royal Academy of Engineering
  6. Wellcome Trust [203139/Z/16/Z, H2R00080, WT088877/Z/09/Z]

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This study explored the contribution of NOEs in ischemic stroke using a 4-pool Bloch-McConnell model and compared it with an approximate 3-pool model. The results showed that the 4-pool model had a stronger ability to distinguish pathological tissue in stroke and exhibited different associations with tissue outcome compared to the 3-pool approximation.
Purpose In chemical exchange saturation transfer imaging, saturation effects between -2 to -5 ppm (nuclear Overhauser effects, NOEs) have been shown to exhibit contrast in preclinical stroke models. Our previous work on NOEs in human stroke used an analysis model that combined NOEs and semisolid MT; however their combination might feasibly have reduced sensitivity to changes in NOEs. The aim of this study was to explore the information a 4-pool Bloch-McConnell model provides about the NOE contribution in ischemic stroke, contrasting that with an intentionally approximate 3-pool model. Methods MRI data from 12 patients presenting with ischemic stroke were retrospectively analyzed, as well as from six animals induced with an ischemic lesion. Two Bloch-McConnell models (4 pools, and a 3-pool approximation) were compared for their ability to distinguish pathological tissue in acute stroke. The association of NOEs with pH was also explored, using pH phantoms that mimic the intracellular environment of naive mouse brain. Results The 4-pool measure of NOEs exhibited a different association with tissue outcome compared to 3-pool approximation in the ischemic core and in tissue that underwent delayed infarction. In the ischemic core, the 4-pool measure was elevated in patient white matter (1.20 +/- 0.20) and in animals (1.27 +/- 0.20). In the naive brain pH phantoms, significant positive correlation between the NOE and pH was observed. Conclusion Associations of NOEs with tissue pathology were found using the 4-pool metric that were not observed using the 3-pool approximation. The 4-pool model more adequately captured in vivo changes in NOEs and revealed trends depending on tissue pathology in stroke.

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