Abstract
Aripiprazole is a novel antipsychotic medication characterized by partial agonism at the D2 and 5-HT1A receptors and by antagonism at the 5-HT2A receptor. The aim of the present study was to evaluate, in an open-label pilot study, the effects and safety of very small doses of aripiprazole on L-dopa-induced dyskinesia of a group of PD patients who did not show a significant clinical benefit by pharmacological treatment with amantadine and mirtazapine. Twelve PD patients with peak-dose LID were enrolled in a period of 1 year. Aripiprazole dosage was of 0.625 mg/day. The ten patients who continued taking aripiprazole displayed a significant decrease in the intensity and frequency of dyskinesias in all parts of the body, particularly in trunk movements (AIMS score T(0) = 14.1 +/- 3.6 vs. final score 2.4. +/- 2.6; P = 0.005). Our study suggests that aripiprazole at very low doses is tolerated and could be efficacy in treating LID.
Publication types
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Clinical Trial
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Research Support, Non-U.S. Gov't
MeSH terms
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Adrenergic alpha-Antagonists / pharmacology
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Aged
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Aged, 80 and over
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Amantadine / pharmacology
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Antiparkinson Agents / adverse effects
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Antiparkinson Agents / antagonists & inhibitors
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Antipsychotic Agents / administration & dosage*
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Antipsychotic Agents / adverse effects
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Aripiprazole
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Basal Ganglia / drug effects
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Basal Ganglia / metabolism
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Basal Ganglia / physiopathology
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Dopamine / metabolism
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Dose-Response Relationship, Drug
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Drug Interactions / physiology
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Dyskinesia, Drug-Induced / drug therapy*
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Dyskinesia, Drug-Induced / metabolism
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Dyskinesia, Drug-Induced / physiopathology
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Female
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Humans
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Levodopa / adverse effects*
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Levodopa / antagonists & inhibitors*
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Male
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Mianserin / analogs & derivatives
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Mianserin / pharmacology
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Middle Aged
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Mirtazapine
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Pilot Projects
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Piperazines / administration & dosage*
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Piperazines / adverse effects
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Quinolones / administration & dosage*
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Quinolones / adverse effects
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Receptors, Dopamine D2 / agonists
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Receptors, Dopamine D2 / metabolism
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Receptors, Serotonin / drug effects
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Receptors, Serotonin / metabolism
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Treatment Outcome
Substances
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Adrenergic alpha-Antagonists
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Antiparkinson Agents
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Antipsychotic Agents
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Piperazines
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Quinolones
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Receptors, Dopamine D2
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Receptors, Serotonin
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Mianserin
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Levodopa
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Aripiprazole
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Mirtazapine
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Amantadine
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Dopamine