## Abstract A two‐dimensional spectroscopic imaging sequence consisting of an inversion recovery pulse, a plane selective prefocused pulse, and a semiselective water suppression pulse has been used to create ^1^H spectroscopic images of the human brain with nominal voxels of 0.5 cc. Due to the exce
Evaluation of multiple sclerosis by 1H spectroscopic imaging at 4.1 T
✍ Scribed by Jullie W. Pan; Hoby P. Hetherington; J. Thomas Vaughan; Galen Mitchell; Gerald M. Pohost; John N. Whitaker
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 692 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0740-3194
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The authors report on high‐field (4.1 T) magnetic resonance ^1^H spectroscopic imaging studies on eight patients with relapsing remitting multiple sclerosis (mean expanded disability status scale (EDSS) 1.0) and eight normal controls. Using T~1~ weighted imaging to determine lesion position, the authors found the ratios of choline/N‐acetyl (NA) compounds and creatine/NA were increased significantly in the multiple sclerosis (MS) patients relative to controls in lesioned tissue, adjacent to lesion, far removed from lesions as well as in periventricular tissue. The gray matter creatine/NA was mildly increased (P < 0.01) in the MS patients, whereas the elevated gray‐matter ratio of choline/NA was of borderline significance (P = 0.13). A more detailed comparison of white‐matter and mean graymatter metabolite values indicates that creatine is increased greatest in areas far from lesions. This is in contrast to choline, which was greatest in lesions, and NA, which was smallest in lesions. It is postulated that the creatine increase may reflect an astrocytic (gliotic) or oligodendrocytic remyelinating process. The increased choline most likely reflects varying levels of inflammation and membrane turnover, whereas the NA decrease is representative of axonal dysfunction or loss.
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