Jc. Fulton et al., MR lesion load and cognitive function in patients with relapsing-remittingmultiple sclerosis, AM J NEUROR, 20(10), 1999, pp. 1951-1955
Citations number
41
Categorie Soggetti
Radiology ,Nuclear Medicine & Imaging","Neurosciences & Behavoir
BACKGROUND AND PURPOSE: Multiple sclerosis (MS) is a demyelinating disease
most often associated with progressive physical impairment; however, its ef
fects are noted to extend beyond physical disability, Our purpose was to de
termine the relationship between T2 lesion volume and neurocognitive and ph
ysical disability in relapsing-remitting multiple sclerosis,
METHODS: We studied a cohort of 19 patients with relapsing-remitting MS. Of
this group, there were 15 women and four men from varying socioeconomic ba
ckgrounds. This volunteer sample was selected from a larger group of 53 pat
ients with MS in our longitudinal MS study because they had been untreated
with any beta-interferon medications, had been followed for at least 12 mon
ths, and had a clinical status of relapsing-remitting MS.
RESULTS: Of 12 neurocognitive parameters tested, two correlated significant
ly with lesion loads. The correlation of the Symbol-Digit Modalities test,
which analyzes information-processing speed, was significant (P = .0204), T
he correlation of the fifth trial of the Rey Auditory Verbal Learning test,
which tests verbal long-term memory, was also significant (P = .0348), Non
e of the other 10 neurocognitive examinations, however, showed a significan
t correlation with total lesion volume (Paced Auditory Serial Addition test
-1.6, P = .7381; Paced Auditory Serial Addition test-2.0, P = .4180; Contro
lled Oral Word Association test, P = .8906; Category Fluency test, P = .442
3; Bells test, P = .9097; Rey Auditory Verbal Learning test-delay, P = .984
3, Rey Auditory Verbal Learning test-recognition, P = .7467; Word Span test
, P = .4939; Road Map test, P = 0.4939). The lesion load also did not corre
late with the physical disability scales as rated according to the Expanded
Disability Status Scale (P = .68) or Ambulation Index (P = .95),
CONCLUSION: Our results indicate that T2 lesion volume does not seem to be
a robust surrogate marker of neuropsychological impairment in patients with
MS. We think that global measurements of parameters that are more specific
to the disease process may offer more precise correlation with cognitive d
ysfunction and other disability parameters.