van Waesberghe, JHTM; Kamphorst, W; De Groot, CJA; van Walderveen, MAA; Castelijns, JA; Ravid, R; ... Barkhof, F; + view all van Waesberghe, JHTM; Kamphorst, W; De Groot, CJA; van Walderveen, MAA; Castelijns, JA; Ravid, R; Nijeholt, GJLA; van der Valk, P; Polman, CH; Thompson, AJ; Barkhof, F; - view fewer (1999) Axonal loss in multiple sclerosis lesions: Magnetic resonance imaging insights into substrates of disability. ANN NEUROL , 46 (5) 747 - 754.
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Magnetic resonance imaging (MRT) monitoring of disease progression in multiple sclerosis is limited by the lack of correlation of abnormalities seen on T2-weighted imaging, and disability. We studied the histopathology of multiple sclerosis lesions, as depicted by MRI, in a large postmortem sample, focusing on axonal loss. Tissue samples from 17 patients were selected immediately postmortem for histopathological analysis on the basis of T2-weighted imaging, including normal appearing white matter and T1 hypointense lesions. In each region, we measured magnetization transfer ratios (MTR), T1 contrast ratio, myelin, and axonal density. T2 lesions (109 samples) mere heterogeneous with regard to MRI appearance on T1 and MTR, whereas axonal density ranged from 0% (no residual axons) to 100% (normal axonal density). Of 64 T2 lesions, 17 were reactive (mild perivascular inflammation only), 21 active, 15 chronically active, and 11 chronically inactive. MTR and T1 contrast ratio correlated strongly with axonal density. Also in normal appearing white matter (24 samples), MTR correlated with axonal density. In conclusion, postmortem tissue sampling by using MRI revealed a range of pathology, illustrating the high sensitivity and low specificity of T2-weighted imaging. T1 hypointensity and MTR were strongly associated with axonal density, emphasizing their role in monitoring progression in multiple sclerosis.
|Title:||Axonal loss in multiple sclerosis lesions: Magnetic resonance imaging insights into substrates of disability|
|Keywords:||HYPOINTENSE LESIONS, SPECTROSCOPY, MRI, DEMYELINATION, PATHOLOGY, DISEASE|
|UCL classification:||UCL > School of Life and Medical Sciences > Faculty of Brain Sciences|
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