Gjla. Nijeholt et al., Magnetization transfer ratio of the spinal cord in multiple sclerosis: Relationship to atrophy and neurologic disability, J NEUROIMAG, 10(2), 2000, pp. 67-72
The authors compare the spinal cord magnetization transfer ratio (MTR) of m
ultiple sclerosis (MS) patients to healthy volunteers, relate MTR to spinal
cord atrophy, and relate these and other magnetic resonance (MR) imaging p
arameters to disability. Sixty-five patients with MS (14 relapsing remittin
g [RR], 34 secondary progressive [SP], and 17 primary progressive [PP] MS),
and 9 healthy volunteers were studied using MR at 1.0 T. Disability of the
patients was assessed using the expanded disability status scale (EDSS). M
agnetic resonance parameters were upper spinal cord MTR, number of focal sp
inal lesions, presence of diffuse abnormalities, and spinal cord cross-sect
ional area (CSA). Correlations were assessed using Spearman's rank correlat
ion coefficient (r). Magnetization transfer ratio was higher in the control
s (median, 33%; range, 30%-38%) than in patients with MS (median, 30%; rang
e, 16-36; p < 0.05). In patients with MS, EDSS correlated with spinal cord
MTR, albeit weakly (r = -0.25, p < 0.05). Correlation between EDSS and spin
al cord CSA was better (SRCC = -0.40, p < 0.01). No correlation was found b
etween MTR and CSA (r = 0.1, p = 0.4). Combining MTR with spinal cord CSA i
mproved correlation with EDSS (r = -0.46, p < 0.001), suggesting an indepen
dent correlation between disability and these 2 MR parameters. Expanded dis
ability status scale scores were higher in patients who had diffuse spinal
cord abnormality regardless of focal lesions (median, 6; range, 1.5-7.5) th
an in patients without diffuse abnormalities (median, 3.5; range, 0-8; p <
0.01). CSA was lower in patients with diffuse spinal cord abnormality (medi
an, 62; range, 46-89 2) than in patients without diffuse abnormalities (med
ian, mm 73; range, 47-89 mm(2); p < 0.01). MTR was slightly lower in patien
ts with diffuse spinal cord abnormalities (median, 29; range, 21%-33%) than
in patients without diffuse abnormalties (median, 31, range, 16-36; t-test
, p < 0.05).