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Washington
(H24N).
Researchers have discovered what they hope is an effective way to
slow the debilitating effects of multiple sclerosis (MS).
MS
is an autoimmune disorder of the central nervous system that usually
appears in women 20-40 years of age. It gradually paralyzes them
by destroying the protective myelin sheaths around the nerves that
allow messages from the brain to get to the muscles.
The
first symptoms of MS are mild and usually come and go. Patients
may experience difficulty seeing (optic neuritis), muscle weakness
(incomplete transverse myelitis), or tingling and numbness in the
fingers and toes (brain stem or cerebellar syndrome). Doctors have
discovered that the longer the time between these first symptoms
and a second episode, the slower the disease progresses and the
better the patient's long-term outcome. Now physicians working in
50 medical centers in the United States and Canada have discovered
that giving beta interferon as soon as multiple sclerosis is diagnosed
significantly prolongs the interval between that first and second
set of symptoms.
Beta
interferon has been used to treat multiple sclerosis for many years,
but only after the disease is well established. The drug slows the
progress of physical disability, reduces the number of relapses
and reduces the number of brain neurons that lose their myelin sheaths
(and show up on magnetic resonance imaging [MRI] scans of the brain).
The question was whether the drug would produce the same good effects
on early disease. The multicenter study, called CHAMPS, published
Sept. 27 in The New England Journal of Medicine proved that
it did.
A
group of 383 patients who had experienced their first set of multiple
sclerosis symptoms and also had less myelin around their brain neurons
on MRI scans received either weekly shots of beta interferon or
a placebo between April of 1996 and March of 2000. If a second episode
of symptoms occurred, patients were withdrawn from the study and
placed on appropriate treatment. At the end of three years, the
patients who received beta interferon had developed a second set
of symptoms only half as often as those who received placebo, with
no serious adverse effects from the drug. Repeat MRI scans showed
that interferon had arrested the disease almost as soon as it was
administered. Further follow-up is necessary to determine the long-term
effects of early beta interferon treatment, but the results of the
CHAMPS study have given physicians and patients fighting the disease
another effective weapon in their arsenal.
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