A Double-Blind, Placebo-Controlled Study of the
Use of Amphetamine in the Treatment of Aphasia

by
Walker-Batson D, Curtis S, Natarajan R, Ford J,
Dronkers N, Salmeron E, Lai J, Unwin DH.
Stroke Center-Dallas,
Department of Communication Sciences & Disorders,
Texas Woman's University (D.W.-B., S.C., J.F.),
The Mobility Foundation Center and Department of Neurology,
University of Texas Southwestern Medical Center (D.W.-B., D.H.U.),
and
the Department of Statistical Science,
Southern Methodist University (R.N.),
Dallas, Tex.
Stroke 2001 Sep 1; 32(9):2093-2098


ABSTRACT

Background and Purpose-- A number of studies suggest that drugs which increase the release of norepinephrine promote recovery when administered late (days to weeks) after brain injury in animals. A small number of clinical studies have investigated the effects of the noradrenergic agonist dextroamphetamine in patients recovering from motor deficits following stroke. To determine whether these findings extend to communication deficits subsequent to stroke, we administered dextroamphetamine, paired with speech/language therapy, to patients with aphasia. METHODS: In a prospective, double-blind study, 21 aphasic patients with an acute nonhemorrhagic infarction were randomly assigned to receive either 10 mg dextroamphetamine or a placebo. Patients were entered between days 16 and 45 after onset and were treated on a 3-day/4-day schedule for 10 sessions. Thirty minutes after drug/placebo administration, subjects received a 1-hour session of speech/language therapy. The Porch Index of Communicative Ability was used at baseline, at 1 week off the drug, and at 6 months after onset as the dependent language measure. RESULTS: Although there were no differences between the drug and placebo groups before treatment (P=0.807), by 1 week after the 10 drug treatments ended there was a significant difference in gain scores between the groups (P=0.0153), with the greater gain in the dextroamphetamine group. The difference was still significant when corrected for initial aphasia severity and age. At the 6-month follow-up, the difference in gain scores between the groups had increased; however, the difference was not significant (P=0.0482) after correction for multiple comparisons. CONCLUSIONS: Administration of dextroamphetamine paired with 10 1-hour sessions of speech/language therapy facilitated recovery from aphasia in a small group of patients in the subacute period after stroke. Neuromodulation with dextroamphetamine, and perhaps other drugs that increase central nervous system noradrenaline levels, may facilitate recovery when paired with focused behavioral treatment.
Dopamine
Neurotoxicity
VTA/glutamate
CNS stimulants
Self-medication
Worms on speed
Dopamine uptake
Canine narcolepsy
Appetite suppressants
Methamphetamine psychosis
Methamphetamine/narcolepsy
Methylphenidate and dopamine



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