Journal of neuroimaging : official journal of the American Society of Neuroimaging
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During the past 10 years, conventional magnetic resonance imaging (cMRI) has become an established tool for the assessment of patients with multiple sclerosis (MS) and to monitor treatment trials. This is mainly due to the sensitivity and reproducibility of cMRI in the detection of MS-related damage. ⋯ Despite the fact that the role of cMRI in MS has been profoundly obviated by the advent of modern and quantitative MR techniques, several issues are still unresolved. Technical development in acquisition and postprocessing, as well as the introduction of high-field magnets in the clinical arena, are likely to increase our understanding of disease pathobiology, mainly through an increased ability to quantify the extent of gray matter damage.
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In the last decade, the use of magnetic resonance imaging (MRI) has led to a reevaluation of the pathogenesis and the natural history of multiple sclerosis (MS). This has been driven to a significant degree by results of proton magnetic resonance spectroscopy (1H-MRS) studies. By providing evidence of early neurodegeneration (based on levels of N-acetylaspartate), results of 1H-MRS studies have led to a reconsideration of the role of axonal damage in MS. ⋯ However, despite the pathological specificity of 1H-MRS and the relatively large number of clinical 1H-MRS studies on patients with MS, measures provided by this MR technique are not used routinely for assessing and monitoring MS patients. This is due to technical difficulties and limitations that are at present not entirely solved. We will review here the most relevant results in MS studies that have used 1H-MRS measures, the clinical importance of these results and the pending issues that need to be solved for a larger and more reliable use of 1H-MRS in clinical MS studies.