## Abstract In the search for proteins that might play a role in the pathogenesis of multiple sclerosis (MS), osteopontin (OPN) has been identified as the most prominent cytokine‐encoding gene expressed within MS lesions. Here, we report significantly increased OPN protein levels in plasma of relap
Diffusely elevated cerebral choline and creatine in relapsing-remitting multiple sclerosis
✍ Scribed by Matilde Inglese; Belinda S.Y. Li; Henry Rusinek; James S. Babb; Robert I. Grossman; Oded Gonen
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 250 KB
- Volume
- 50
- Category
- Article
- ISSN
- 0740-3194
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
It is well known that multiple sclerosis (MS) pathogenesis continues even during periods of clinical silence. To quantify the metabolic characteristics of this activity we compared the absolute levels of N‐acetylaspartate (NAA), creatine (Cr), and choline (Cho) in the normal‐appearing white matter (NAWM) between relapsing‐remitting (RR) MS patients and controls. Metabolite concentrations were obtained with 3D proton MR spectroscopy at 1.5 T in a 480 cm^3^ volume‐of‐interest (VOI), centered on the corpus callosum of 11 MS patients and 9 matched controls. Gray/white‐matter/cerebral‐spinal‐fluid (CSF) volumes were obtained from MRI segmentation. Patients' average VOI tissue volume (V~T~), 410.8 ± 24.0 cm^3^, and metabolite levels, NAA = 6.33 ± 0.70, Cr = 4.67 ± 0.52, Cho = 1.40 ± 0.17 mM, were different from the controls by –8%, –9%, +22% and +32%. The Cho level was the only single metric differentiating patients from controls at 100% specificity and >90% sensitivity. Diffusely elevated Cho and Cr probably reflect widespread microscopic inflammation, gliosis, or de‐ and remyelination in the NAWM. Both metabolites are potential prognostic indicators of current disease activity, preceding NAA decline and atrophy. Magn Reson Med 50:190–195, 2003. © 2003 Wiley‐Liss, Inc.
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