Synopsis
The spinal cord is heavily affected in multiple sclerosis and
several other demyelinating conditions. This talk will describe MRI findings in
spinal cord demyelinating diseases; challenges in successfully imaging the
spinal cord, as well as ways of overcoming those challenges; and recent
improvements in spinal cord structural MRI as applied to multiple sclerosis.
The spinal cord is heavily affected in multiple sclerosis
(MS) and several other demyelinating conditions. At least 90% of MS cases have
inflammatory demyelinating lesions in the spinal cord. MRI detects cord lesions
in most cases at the time of diagnosis, and establishing their presence fulfills
one of the 2010 McDonald criteria for dissemination in space. Damage to the
cord, including both focal demyelination and neuroaxonal degeneration,
contributes massively to disability, particularly in the progressive stage of
the disease. Finally, the spinal cord is an attractive target structure for
studies that seek to elucidate the functional correlates of MRI-visualized
tissue damage in MS. Unfortunately, however, despite its importance, spinal
cord imaging has proven to be especially challenging for a variety of technical
reasons. As such, its potential value for the care of the MS patient, and for
improving understanding of the disease in general, is underappreciated.
In this lecture, I will show how MRI can detect spinal cord
involvement in MS. I will also describe the findings in diseases that have
comparable effects on the MRI appearance of the spinal cord, such as neuromyelitis
optica spectrum disorder, infectious myelitis including human T-lymphotropic
virus-associated myelopathy/tropical spastic paraparesis, subacute combined
degeneration, and copper deficiency myelopathy. I will present recent
improvements in spinal cord structural MRI as applied to MS and will show how
those improvements can be used to detect lesions more reliably. I will mention approaches
to measuring spinal cord atrophy, which has proven to be a relatively strong
marker of disease progression. Finally, I will show how quantitative MRI
techniques that are sensitive to tissue structure on a subvoxel level, such as
diffusion-weighted and magnetization-transfer imaging, can be useful adjuncts
to improved structural imaging techniques despite being pathologically
nonspecific.
Acknowledgements
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