Objective: The present study was initiated to evaluate a possible relationship between CD14 monocyte receptor genetic polymorphism and the risk of Parkinson's disease (PD). Background: Inflammatory processes have been postulated to play a role in the pathogenesis of PD. The C(Ϫ260) 3 T polymorphism
Poster session 4, Abstracts 1167–1209
- Book ID
- 102503212
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 173 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0885-3185
No coin nor oath required. For personal study only.
✦ Synopsis
Objective: To describe our preliminary experience on the use of aripiprazole for drug-induced psychosis (DIP) in Parkinson's disease (PD).
Background: Aripiprazole is the newest atypical antipsychotic (AA) drug to be released in the US. It is the only AA that is a partial agonist at the D2 and 5HT1a receptors and an antagonist at 5HT2a receptors. It also has a high 5HT2/D2 ratio and may therefore carry a low risk of extrapyramidal side effects and alleviate psychosis in parkinson-vulnerable populations.
Methods: We report a series of eight patients with probable PD treated with aripiprazole for DIP. Aripiprazole was started at 5-10 mg/day and slowly increased over 3-7 days until side effects or improvement of psychosis occurred.
Results: Two patients were neuroleptic-naive, five patients were "quetiapine failures," and one patient was switched from olanzapine to aripiprazole. Only 2 out of 8 patients experienced near complete resolution of their psychosis using aripiprazole. The other six patients discontinued aripiprazole within 40 days, 2 of whom discontinued due to motor worsening.
Conclusion: Our preliminary experience with aripiprazole is mixed but not very encouraging. Controlled studies are needed to evaluate aripiprazole in parkinsonian patients.
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