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Long T2 water in multiple sclerosis: what else can we learn from multi-echo T2 relaxation?
Cornelia Laule1, Irene M Vavasour, Shannon H Kolind
1Department of Radiology, University of British Columbia Hospital Room M10 Purdy Pavilion/ECU, 2221 Wesbrook Mall, Vancouver BC V6T 2B5, Canada. claule@physics.ubc.ca
Journal of Neurology
|September 1, 2007
Summary
Multi-echo T(2) measurements reveal distinct water reservoirs in multiple sclerosis (MS) lesions. Characterizing longer T(2) components may improve understanding of MS pathology and disease duration.
Area of Science:
- Neuroimaging
- Magnetic Resonance Imaging (MRI)
- Multiple Sclerosis (MS) Research
Background:
- Multi-echo T(2) measurements are crucial for understanding brain pathology in multiple sclerosis (MS).
- The T(2) distribution can reveal additional water reservoirs linked to inflammation or edema beyond myelin and total water content.
- Characterizing longer T(2) components in MS lesions and normal-appearing white matter (NAWM) is essential for a comprehensive understanding.
Purpose of the Study:
- To better define the T(2) distribution in MS lesions and NAWM.
- To specifically characterize the longer T(2) components within these regions.
- To investigate the relationship between these T(2) characteristics and clinical/imaging parameters.
Main Methods:
- Acquisition of magnetisation transfer (MT), T(1), and 48-echo T(2) relaxation data from 20 MS subjects.
- Defining regions of interest (ROIs) in both MS lesions and NAWM.
- Analysis of T(2) distribution, geometric mean T(2) (GMT(2)), water content (WC), T(1), magnetisation transfer ratio (MTR), and myelin water fraction (MWF).
Main Results:
- Twenty-seven out of 107 lesions exhibited a markedly prolonged T(2) signal (200-800 ms).
- Lesions with a Long-T(2) signal showed higher GMT(2), WC, and T(1), with reduced MTR and myelin water fraction (MWF) compared to other lesions.
- Subjects with Long-T(2) lesions had significantly longer disease duration; strong correlations found between T(1) and Long-T(2) fraction.
Conclusions:
- A potential source of the Long-T(2) signal in MS lesions is increased extracellular water.
- This study underscores the utility of extending the data acquisition window in multi-echo T(2) relaxation sequences for improved MS characterization.
- Longer T(2) components provide valuable insights into MS pathology and disease progression.
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