Abstract | INTRODUCTION: METHODS: Post-hoc analysis using pooled data from two extended-release amantadine pivotal trials and follow-on open-label extension. Dystonia was assessed using the Unified Dyskinesia Rating Scale (UDysRS) Part 2 and the Movement Disorder Society-Unified PD Rating Scale (MDS-UPDRS) item 4.6. RESULTS: Of 196 participants, 119 (60.7%) reported OFF-related dystonia at baseline per UDysRS. Twelve-week treatment with extended-release amantadine improved OFF dystonia (treatment differences vs placebo: UDysRS Part 2, -1.0 [-1.9,-0.1]; p = 0.03 and MDS-UPDRS Item 4.6, -0.3 [-0.6,-0.05]; p = 0.02). There was no correlation between changes in OFF time and changes in OFF dystonia. Double-blind improvements in OFF dystonia were sustained throughout the 2-year follow-up. CONCLUSIONS: Extended-release amantadine yielded a sustained reduction in OFF-related dystonia in PD patients that was independent from a reduction in OFF time. A randomized controlled trial is warranted to confirm these findings.
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Authors | Alberto J Espay, Jill L Ostrem, Andrea E Formella, Caroline M Tanner |
Journal | Parkinsonism & related disorders
(Parkinsonism Relat Disord)
Vol. 122
Pg. 106088
(May 2024)
ISSN: 1873-5126 [Electronic] England |
PMID | 38461688
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Randomized Controlled Trial)
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Copyright | Copyright © 2024 The Authors. Published by Elsevier Ltd.. All rights reserved. |
Chemical References |
- Amantadine
- Delayed-Action Preparations
- Antiparkinson Agents
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Topics |
- Humans
- Amantadine
(administration & dosage)
- Parkinson Disease
(complications, drug therapy)
- Male
- Female
- Delayed-Action Preparations
- Dystonia
(drug therapy, etiology)
- Aged
- Middle Aged
- Antiparkinson Agents
(administration & dosage)
- Double-Blind Method
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