Although a more favorable course of multiple sclerosis is associated with a low degree of cortical pathology, only longitudinal studies could definitely confirm this association.
MATERIALS AND METHODS: We
followed 95 early relapsing-remitting MS (RRMS; median Expanded
Disability Status Scale (EDSS) = 1.5, mean disease duration = 3.1 ± 1.3
years) and 45 benign MS patients (EDSS ≤ 3.0, disease duration ≥ 15
years, normal cognition) for 6 years, with EDSS evaluations every 6
months and brain magnetic resonance imaging (MRI) at baseline and then
yearly.
RESULTS: At baseline, we detected 406 cortical
lesions (CLs) in 67/95 (70.5%) early RRMS and in 24/45 (53.3%) benign MS
patients (p = 0.046). After 6 years, the appearance of new CLs was
observed in 80/95 (84.2%; 518 CLs) of our early RRMS and in 25/45
(55.5%; 63 CLs; p < 0.001) benign MS patients. At baseline, after
corrections for age and disease duration, we observed a cortical
thinning of several frontal and temporal regions in our RRMS study
patients, compared to the benign MS patients (p ranging between
0.001-0.05). After 6 years, the cortical thinning had increased
significantly in several cortices of RRMS patients, but only in the
occipital-temporal (p = 0.036) and superior parietal gyrus (p = 0.035)
of those with benign MS. Stepwise regression analysis revealed the CL
volume (p = 0.006) and the cortical thickness of the temporal middle (p
< 0.001), insular long (p < 0.001), superior frontal (p <
0.001) and middle frontal gyri (p < 0.001) as the most sensitive
independent predictors of a favorable disease course.
CONCLUSIONS:Our
data confirmed that a significantly milder cortical pathology
characterizes the most favorable clinical course of MS. Measures of
focal and diffuse grey matter should be combined to increase the
accuracy in the identification of a benign MS course.
The results show that if there is thinning of the grey matter of the brain then this is more likely to be associated with more disability and indicates the more nerve loss that occurs the more likely that disability progresses
Labels: Cortical Lesions, Progression