I read the recent report on magnetization transfer ratio as a marker for myelin in multiple sclerosis with a great interest (1). Vavasour et al concluded that ''MTR was correlated with WC in MS tissue, indicating that inflammation and edema influence MTR (1).'' This finding is very interesting. Howe
Magnetization transfer ratio evolution with demyelination and remyelination in multiple sclerosis lesions
β Scribed by Jacqueline T. Chen; D. Louis Collins; Harold L. Atkins; Mark S. Freedman; Douglas L. Arnold
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 795 KB
- Volume
- 63
- Category
- Article
- ISSN
- 0364-5134
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
Objective
To assess demyelination and remyelination in vivo in acute gadolinium (Gd)βenhancing lesions of multiple sclerosis (MS).
Methods
We measured significant changes in magnetization transfer ratio (MTR) consistent with demyelination and remyelination of individual lesion voxels, as well as the mean normalized MTR over all lesion voxels during and after contrast enhancement, in MS patients participating in a 3βyear Canadian trial assessing immunoablation and autologous stem cell transplantation for treatment of MS.
Results
The average mean normalized lesion MTR over all lesions exhibited partial recovery over 2 to 4 months after Gd enhancement. Voxelβbased analysis demonstrated that approximately 70% of the initially enhancing lesion volume (GdLV) was left with stably low MTR over 39 months of evaluation. The percentage of the GdLV undergoing significant increases in MTR consistent with remyelination increased for approximately 7 months after enhancement and then stabilized at 21 %GdLV. Significant decreases in MTR consistent with demyelination were ongoing for approximately 33 months after enhancement, stabilizing at 9 %GdLV. The estimated error of these measurements, based on scan/rescan analysis, was less than 0.4 %GdLV.
Interpretation
We found significant changes in MTR consistent with demyelination and remyelination that followed different temporal evolutions and were ongoing in different lesion regions for at least 3 years after lesion formation. Ann Neurol 2008
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