TitleThe effects of amantadine and pemoline on cognitive functioning in multiple sclerosis.
Publication TypeJournal Article
Year of Publication1996
AuthorsGeisler, MW, Sliwinski, M, Coyle, PK, Masur, DM, Doscher, C, Krupp, LB
JournalArch Neurol
Volume53
Issue2
Pagination185-8
Date Published1996 Feb
ISSN0003-9942
KeywordsAdolescent, Adult, Amantadine, Analysis of Variance, Attention, Central Nervous System Stimulants, Cognition, Fatigue, Female, Humans, Male, Memory, Middle Aged, Movement, Multiple Sclerosis, Neuropsychological Tests, Pemoline
Abstract

<p><b>BACKGROUND: </b>Amantadine hydrochloride and pemoline, both frequently used to treat the fatigue of multiple sclerosis (MS), may also improve attention and other cognitive functions in MS. To our knowledge, these agents have never been compared in a placebo-controlled trial of patients with MS.</p><p><b>OBJECTIVE: </b>To evaluate the effects of amantadine and pemoline on cognitive functioning in MS.</p><p><b>METHODS: </b>A total of 45 ambulatory patients with MS and severe fatigue were treated for 6 weeks with amantadine, pemoline, or placebo using a parallel group design. They underwent comprehensive neuropsychological testing to determine treatment effects on cognitive functioning. Primary outcome measures were tests of attention (Digit Span, Trail Making Test, and Symbol Digit Modalities Test), verbal memory (Selective Reminding Test), nonverbal memory (Benton Visual Retention Test), and motor speed (Finger Tapping Test).</p><p><b>RESULTS: </b>Fatigue did not significantly correlate with any of the neuropsychological outcome measures at baseline or after treatment. All three treatment groups improved on tests of attention (P < .003), verbal memory (P < .001), and motor speed (P < .002). There were no significant differences between amantadine, pemoline, and placebo.</p><p><b>CONCLUSIONS: </b>Cognitive functioning in MS is independent of fatigue. Neither amantadine nor pemoline enhances cognitive performance in MS compared with placebo.</p>

DOI10.1001/archneur.1996.00550020101021
Alternate JournalArch Neurol
PubMed ID8639070
Grant ListA13156 / / PHS HHS / United States