Safety and Efficacy of Levetiracetam for the Management of Levodopa- Induced Dyskinesia in Patients with Parkinson’s Disease: A Systematic Review
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Published:2019-07-17
Issue:4
Volume:18
Page:317-325
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ISSN:1871-5273
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Container-title:CNS & Neurological Disorders - Drug Targets
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language:en
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Short-container-title:CNSNDDT
Author:
Ebada Mahmoud A.1, Alkanj Souad1, Ebada Mohamed2, Abdelkarim Ahmed H.1, Diab Ahmed3, Aziz Mohamed A.E.4, Soliman Ahmed M.5, Fayed Notila1, Bahbah Eshak I.5, Negida Ahmed1
Affiliation:
1. Faculty of Medicine, Zagazig University, Zagazig, Egypt 2. Al-Ahrar Teaching Hospital, Kafr El-Ahrar, Egypt 3. Faculty of Medicine, Ain Shams University, Cairo, Egypt 4. Omr Shahin Mental Hospital, Egypt 5. Faculty of Medicine, Al-Azhar University, Damietta, Egypt
Abstract
Background:
Levetiracetam, a novel antiepileptic drug, has shown antidyskinetic effects in
experimental animal models of Parkinson's disease (PD). The tolerability and efficacy of levetiracetam
in reducing the levodopa-induced dyskinesia (LID) in PD patients have not been established. Therefore,
this study aims to synthesize evidence from published prospective clinical trials about the efficacy
of levetiracetam for the management of LID in PD patients.
Methods:
We followed the PRISMA statement guidelines during the preparation of this systematic review.
A computer literature search of PubMed, EBSCO, Scopus, MEDLINE, and the web of science
was carried out. We selected prospective clinical trials assessing the anti-dyskinetic efficacy of
levetiracetam for treating LID in patients with PD. The Abnormal Involuntary Movement Scale
(AIMS), Clinical Global Impression Score (GCI), UPDRS III, and UPDRS IV were considered as the
primary outcome measures; their data were extracted and reviewed.
Results:
Our review included seven clinical trials with a total of 150 patients. Of them, three studies
were randomized controlled trials, and the remaining were open-label single arm trials. Four studies
reported poor tolerability of the levetiracetam with mild anti-dyskinetic effects. Levetiracetam slightly
improved the UPDRS-IV and AIMS scores with small effect size. In the remaining three studies,
levetiracetam failed to exhibit any anti-dyskinetic effects.
Conclusion:
Current evidence does not support the efficacy of the levetiracetam for treating LID in
PD patients, however, due to the limited number of published randomized control trials (RCTs), further
RCTs are required.
Publisher
Bentham Science Publishers Ltd.
Subject
Pharmacology,General Neuroscience
Reference40 articles.
1. Negida A, Elfil M, Attia E. CNS Neurol Disord Drug Targets, Caffeine; the forgotten potential for parkinson’s disease.,, 2017, 16,, 652-657, 2. Fatima A, Jyoti S, Siddique YH. CNS Neurol Disord Drug Targets, Models of Parkinson’s disease with special emphasis on drosophila melanogaster.,, 2018, 17,, 757-766, 3. de Farias CC, Maes M, Bonifacio KL. CNS Neurol Disord Drug Targets, Parkinson’s disease is accompanied by intertwined alterations in iron metabolism and activated immune-inflammatory and oxidative stress pathways.,, 2017, 16,, 484-491, 4. Radad K, Moldzio R, Al-Shraim M, Kranner B, Krewenka C, Rausch W-D. CNS Neurol Disord Drug Targets, Recent advances on the role of neurogenesis in the
adult brain: Therapeutic potential in Parkinson’s and Alzheimer's
diseases. CNS Neurol Disord Drug Targets 2017; 16(7): 740-8.
Available from,, , 16,, 484-,28641510 5. Dezsi L, Vecsei L. CNS Neurol Disord Drug Targets, Monoamine oxidase B inhibitors in Parkinson’s disease.,, 2017, 16,, 425-439,
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