Cited 13 time in
- Title
- A novel voxel-wise lesion segmentation technique on 3.0-T diffusion MRI of hyperacute focal cerebral ischemia at 1 h after permanent MCAO in rats
- Author(s)
- C H Choi; K S Yi; Sang-Rae Lee; Youngjeon Lee; Chang Yeop Jeon; J Hwnag; C Lee; S S Choi; H J Lee; S H Cha
- Bibliographic Citation
- Journal of Cerebral Blood Flow and Metabolism, vol. 38, no. 8, pp. 1371-1383
- Publication Year
- 2018
- Abstract
- To assess hyperacute focal cerebral ischemia in rats on 3.0-Tesla diffusion-weighted imaging (DWI), we developed a novel voxel-wise lesion segmentation technique that overcomes intra- and inter-subject variation in apparent diffusion coefficient (ADC) distribution. Our novel technique involves the following: (1) intensity normalization including determination of the optimal type of region of interest (ROI) and its intra- and inter-subject validation, (2) verification of focal cerebral ischemic lesions at 1 h with gross and high-magnification light microscopy of hematoxylin-eosin (H&E) pathology, (3) voxel-wise segmentation on ADC with various thresholds, and (4) calculation of dice indices (DIs) to compare focal cerebral ischemic lesions at 1 h defined by ADC and matching H&E pathology. The best coefficient of variation was the mode of the left hemisphere after normalization using whole left hemispheric ROI, which showed lower intra- (2.54±0.72%) and inter-subject (2.67±0.70%) values than the original. Focal ischemic lesion at 1 h after middle cerebral artery occlusion (MCAO) was confirmed on both gross and microscopic H&E pathology. The 83 relative threshold of normalized ADC showed the highest mean DI (DI=0.820±0.075). We could evaluate hyperacute ischemic lesions at 1 h more reliably on 3-Tesla DWI in rat brains.
- Keyword
- Brain ischemiaacute strokeanimal modelsbrain imagingdiffusion-weighted MRI
- ISSN
- 0271-678X
- Publisher
- Sage
- Full Text Link
- http://dx.doi.org/10.1177/0271678X17714179
- Type
- Article
- Appears in Collections:
- Ochang Branch Institute > Division of National Bio-Infrastructure > National Primate Research Center > 1. Journal Articles
- Files in This Item:
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