Abstract
Background: Dopamine agonists could theoretically normalize the suspected central dopamine hypersensitivity in Tourette's syndrome. Methods: There was a multicenter randomized, placebo-controlled, double-blind clinical trial of pramipexole given for 6 weeks in 63 children and adolescents with Tourette's syndrome. Results: There were no significant differences in the adjusted mean change in the Total Tic Score of the Yale Global Tic Severity Scale for patients treated with pramipexole -7.16) and placebo -7.17). There were no significant treatment effects on change from baseline in the Global Severity score of the Yale Scale and parent- and investigator-scored Clinical Global Impression of Improvement. In patients with attention deficit hyperactivity disorder, there was improvement in DuPaul ADHD scale scores for patients receiving pramipexole compared with placebo. Conclusions: There was no evidence that pramipexole has efficacy in suppressing tics. Pramipexole may decrease symptoms of associated attention deficit hyperactivity disorder.
Original language | English (US) |
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Pages (from-to) | 775-778 |
Number of pages | 4 |
Journal | Movement Disorders |
Volume | 27 |
Issue number | 6 |
DOIs | |
State | Published - May 2012 |
Externally published | Yes |
Keywords
- Dopamine agonist
- Pramipexole
- Tics
- Tourette's syndrome
- Treatment, clinical trial
ASJC Scopus subject areas
- Neurology
- Clinical Neurology