Na. Losseff et Dh. Miller, MEASURES OF BRAIN AND SPINAL-CORD ATROPHY IN MULTIPLE-SCLEROSIS, Journal of Neurology, Neurosurgery and Psychiatry, 64, 1998, pp. 102-105
Although conventional magnetic resonance imaging (MRI) has greatly inc
reased the understanding of the pathophysiology of multiple sclerosis,
its relation to the development of disability is complex. More pathol
ogically specific imaging markers have therefore been sought to try an
d understand the underlying process that is responsible for the progre
ssive disability that so commonly occurs in multiple sclerosis. Of the
se the most simple to understand conceptually is the measurement of at
rophy, which most probably represents axonal loss. Several recent stud
ies have shown that atrophy is a process closely linked with the progr
essive phase of multiple sclerosis and worsening disability. Furthermo
re it has also been shown that atrophy may evolve despite the absence
of inflammatory activity as judged by gadolinium enhanced MRI and thus
its measurement gives information in addition to that obtained from c
onventional MRI. Because of new developments in imaging we are now abl
e to measure atrophy reliably and reproducibly. Hence the measurement
of atrophy now provides objective markers by which to evaluate putativ
e treatment aimed at preventing disability in multiple sclerosis.