posted on 2007-06-14, 11:19authored byMassimo Filippi, Marco Rovaris, R. Capra, C. Gasperini, F. Prandini, V. Martinelli, Mark A. Horsfield, S. Bastianello, Maria Pia Sormani, C. Pozzilli, G. Comi
Objective—The ability of recombinant
human interferon â-1a (rh-IFN â-1a) to
suppress multiple sclerosis activity, evaluated from MRI, was assessed across a
range of lesions enhancing at different
gadolinium-DTPA (Gd) doses and with
different sizes.
Methods—Every 4 weeks, standard dose
(Sd; 0.1 mmol/kg Gd) and triple dose (Td;
0.3 mmol/kgGd) MRI were obtained from
18 patients with relapsing-remitting multiple
sclerosis for 3 months before and 4 months after starting treatment with 44 μg
rh-IFN â-1a subcutaneously, once a week.
Results—The total numbers of enhancing
lesions were 145 and 126 on Sd scans and
278 and 192 on the Td scans obtained
before and after treatment. The introduction
of treatment decreased, on average, the rate of appearance of new enhancing lesions seen on Sd and Td scans by 37% (p<0.001). Treatment effects on new enhancing lesions seen on Td scans was, on average, 28% higher than on those seen on Sd scans. The distribution of lesion sizes on Td scans changed significantly during the treatment period (p=0.05), due to a marked decrease in the number of small lesions.
Conclusions— The effect of 44 μg rh-IFN
â-1a in reducing multiple sclerosis disease
activity, as monitored by Gd enhanced MRI, is not homogeneous, but graduated according to the pathological characteristics and size of the lesions.
History
Citation
Journal of Neurology Neurosurgery and Psychiatry, 1999, 67, pp.386-389.
Published in
Journal of Neurology Neurosurgery and Psychiatry
Publisher
BMJ Publishing Group
Available date
2007-06-14
Notes
This is the version as published in Journal of neurology Neurosurgery and Psychiatry. http://jnnp.bmj.com/