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In vivo 4.0‐T magnetic resonance investigation of spinal cord inflammation, demyelination, and axonal damage in chronic‐progressive experimental allergic encephalomyelitis
Author(s) -
Cook Lisa L.,
Foster Paula J.,
Mitchell J. Ross,
Karlik Stephen J.
Publication year - 2004
Publication title -
journal of magnetic resonance imaging
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.563
H-Index - 160
eISSN - 1522-2586
pISSN - 1053-1807
DOI - 10.1002/jmri.20171
Subject(s) - spinal cord , magnetic resonance imaging , pathology , encephalomyelitis , medicine , white matter , myelin , multiple sclerosis , inflammation , magnetization transfer , central nervous system , central nervous system disease , radiology , immunology , endocrinology , psychiatry
Purpose To image and dissect the lumbar spinal cord of guinea pigs with chronic‐progressive experimental allergic encephalomyelitis (CP‐EAE) and directly correlate the pathology to the magnetic resonance (MR) image data obtained at 4 T and determine if these MR contrasts can accurately differentiate a specific type of pathology from control tissue. Materials and Methods The amount of inflammation, demyelination, and axonal pathology were quantified in the whole cord cross sections. The signal intensities (SIs) for 228 individual regions of interest (ROIs) (normal‐appearing white matter (NAWM) and tissue containing inflammation with or without demyelination) were measured directly from the corresponding area on the MR images. Results Conventional MR contrast SIs and magnetization transfer ratio (MTR) were related to the degree of demyelination and presence of inflammation. MTR and proton density‐weighted (PDw) SIs were both moderately related to axonal density. The SIs for NAWM and in lesions containing both cellular infiltrates and demyelination in all conventional MR contrast images were also increased, whereas the MTR was decreased when compared to control tissue. Conclusion The SIs from the conventional MR contrasts and MTR at 4 T were sensitive to the presence of disease within CP‐EAE spinal cord, but were not specific to the underlying pathology. J. Magn. Reson. Imaging 2004;20:563–571. © 2004 Wiley‐Liss, Inc.