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The effect of istradefylline for Parkinson’s disease: A meta-analysis

Adenosine A(2A) receptor antagonists are an alternative treatment strategy for Parkinson’s disease. Several randomized placebo controlled studies have tested the effect of A(2A) receptor antagonist istradefylline, and more robust evidence has been acquired. This meta-analysis aimed to provide eviden...

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Autores principales: Sako, Wataru, Murakami, Nagahisa, Motohama, Keisuke, Izumi, Yuishin, Kaji, Ryuji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5740127/
https://www.ncbi.nlm.nih.gov/pubmed/29269791
http://dx.doi.org/10.1038/s41598-017-18339-1
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author Sako, Wataru
Murakami, Nagahisa
Motohama, Keisuke
Izumi, Yuishin
Kaji, Ryuji
author_facet Sako, Wataru
Murakami, Nagahisa
Motohama, Keisuke
Izumi, Yuishin
Kaji, Ryuji
author_sort Sako, Wataru
collection PubMed
description Adenosine A(2A) receptor antagonists are an alternative treatment strategy for Parkinson’s disease. Several randomized placebo controlled studies have tested the effect of A(2A) receptor antagonist istradefylline, and more robust evidence has been acquired. This meta-analysis aimed to provide evidence for its efficacy and safety on patients with Parkinson’s disease. After a systematic literature search, we calculated the pooled standardized mean difference and risk ratio for continuous and dichotomous variables, respectively. Further, sensitivity analyses were performed to confirm the effect estimated by meta-analyses. Publication bias was assessed by funnel plot and deviation of intercept. Six studies satisfied our inclusion criteria. Istradefylline (40 mg/day) decreased off time and improved motor symptoms of Parkinson’s disease in homogeneous studies. Istradefylline at 20 mg/day decreased off time and improved motor symptoms, but heterogeneity was found in the analysis of the former among studies. There was a significant effect of istradefylline on dyskinesia in homogeneous studies. Publication bias, however, was observed in the comparison of dyskinesia. Other adverse events showed no significant difference. The present meta-analysis suggests that istradefylline at 40 mg/day could alleviate off time and motor symptoms derived from Parkinson’s disease. Dyskinesia might be worsened, but publication bias prevents this from being clear.
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spelling pubmed-57401272018-01-03 The effect of istradefylline for Parkinson’s disease: A meta-analysis Sako, Wataru Murakami, Nagahisa Motohama, Keisuke Izumi, Yuishin Kaji, Ryuji Sci Rep Article Adenosine A(2A) receptor antagonists are an alternative treatment strategy for Parkinson’s disease. Several randomized placebo controlled studies have tested the effect of A(2A) receptor antagonist istradefylline, and more robust evidence has been acquired. This meta-analysis aimed to provide evidence for its efficacy and safety on patients with Parkinson’s disease. After a systematic literature search, we calculated the pooled standardized mean difference and risk ratio for continuous and dichotomous variables, respectively. Further, sensitivity analyses were performed to confirm the effect estimated by meta-analyses. Publication bias was assessed by funnel plot and deviation of intercept. Six studies satisfied our inclusion criteria. Istradefylline (40 mg/day) decreased off time and improved motor symptoms of Parkinson’s disease in homogeneous studies. Istradefylline at 20 mg/day decreased off time and improved motor symptoms, but heterogeneity was found in the analysis of the former among studies. There was a significant effect of istradefylline on dyskinesia in homogeneous studies. Publication bias, however, was observed in the comparison of dyskinesia. Other adverse events showed no significant difference. The present meta-analysis suggests that istradefylline at 40 mg/day could alleviate off time and motor symptoms derived from Parkinson’s disease. Dyskinesia might be worsened, but publication bias prevents this from being clear. Nature Publishing Group UK 2017-12-21 /pmc/articles/PMC5740127/ /pubmed/29269791 http://dx.doi.org/10.1038/s41598-017-18339-1 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Sako, Wataru
Murakami, Nagahisa
Motohama, Keisuke
Izumi, Yuishin
Kaji, Ryuji
The effect of istradefylline for Parkinson’s disease: A meta-analysis
title The effect of istradefylline for Parkinson’s disease: A meta-analysis
title_full The effect of istradefylline for Parkinson’s disease: A meta-analysis
title_fullStr The effect of istradefylline for Parkinson’s disease: A meta-analysis
title_full_unstemmed The effect of istradefylline for Parkinson’s disease: A meta-analysis
title_short The effect of istradefylline for Parkinson’s disease: A meta-analysis
title_sort effect of istradefylline for parkinson’s disease: a meta-analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5740127/
https://www.ncbi.nlm.nih.gov/pubmed/29269791
http://dx.doi.org/10.1038/s41598-017-18339-1
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