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Long-Term Effects of Safinamide on Mood Fluctuations in Parkinson’s Disease

BACKGROUND: Mood disorders are very frequent in Parkinson’s Disease (PD), and their effective treatment is still a major unresolved issue: growing evidence suggests that glutamatergic system dysfunction is directly involved. Safinamide is a drug with an innovative mechanism of action, dopaminergic a...

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Autores principales: Cattaneo, Carlo, Müller, Thomas, Bonizzoni, Erminio, Lazzeri, Gabriele, Kottakis, Ioannis, Keywood, Charlotte
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5676861/
https://www.ncbi.nlm.nih.gov/pubmed/28777756
http://dx.doi.org/10.3233/JPD-171143
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author Cattaneo, Carlo
Müller, Thomas
Bonizzoni, Erminio
Lazzeri, Gabriele
Kottakis, Ioannis
Keywood, Charlotte
author_facet Cattaneo, Carlo
Müller, Thomas
Bonizzoni, Erminio
Lazzeri, Gabriele
Kottakis, Ioannis
Keywood, Charlotte
author_sort Cattaneo, Carlo
collection PubMed
description BACKGROUND: Mood disorders are very frequent in Parkinson’s Disease (PD), and their effective treatment is still a major unresolved issue: growing evidence suggests that glutamatergic system dysfunction is directly involved. Safinamide is a drug with an innovative mechanism of action, dopaminergic and non-dopaminergic, that includes the reversible inhibition of the monoamine oxidase-B (MAO-B) enzyme and the modulation of excessive glutamate release through the use- and state-dependent blockade of the sodium channels. OBJECTIVE: To investigate the effects of safinamide on mood over two-year treatment in PD patients with motor fluctuations. METHODS: This was a post-hoc analysis of the data from studies 016 and 018. The analysis focused on outcomes related to mood, namely: scores of the “Emotional well-being” domain of the Parkinson’s Disease Questionnaire (PDQ-39), scores of the GRID Hamilton Rating Scale for Depression (GRID-HAMD) and the proportion of patients reporting depression as an adverse event over the entire treatment period. RESULTS: Safinamide, compared to placebo, significantly improved the PDQ-39 “Emotional well-being” domain after6-months (p = 0.0067) and 2 years (p = 0.0006), as well as the GRID-HAMD (p = 0.0408 after 6 months and p = 0.0027 after 2 years). Significantly fewer patients in the safinamide group, compared to placebo, experienced depression as adverse event (p = 0.0444 after 6 months and p = 0.0057 after 2 years). CONCLUSION: The favorable effect of safinamide on mood may be explained by the improvement in wearing off and by its modulation of glutamatergic hyperactivity and reversible MAO-B inhibition. Prospective studies are warranted to investigate this potential benefit.
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spelling pubmed-56768612017-11-16 Long-Term Effects of Safinamide on Mood Fluctuations in Parkinson’s Disease Cattaneo, Carlo Müller, Thomas Bonizzoni, Erminio Lazzeri, Gabriele Kottakis, Ioannis Keywood, Charlotte J Parkinsons Dis Research Report BACKGROUND: Mood disorders are very frequent in Parkinson’s Disease (PD), and their effective treatment is still a major unresolved issue: growing evidence suggests that glutamatergic system dysfunction is directly involved. Safinamide is a drug with an innovative mechanism of action, dopaminergic and non-dopaminergic, that includes the reversible inhibition of the monoamine oxidase-B (MAO-B) enzyme and the modulation of excessive glutamate release through the use- and state-dependent blockade of the sodium channels. OBJECTIVE: To investigate the effects of safinamide on mood over two-year treatment in PD patients with motor fluctuations. METHODS: This was a post-hoc analysis of the data from studies 016 and 018. The analysis focused on outcomes related to mood, namely: scores of the “Emotional well-being” domain of the Parkinson’s Disease Questionnaire (PDQ-39), scores of the GRID Hamilton Rating Scale for Depression (GRID-HAMD) and the proportion of patients reporting depression as an adverse event over the entire treatment period. RESULTS: Safinamide, compared to placebo, significantly improved the PDQ-39 “Emotional well-being” domain after6-months (p = 0.0067) and 2 years (p = 0.0006), as well as the GRID-HAMD (p = 0.0408 after 6 months and p = 0.0027 after 2 years). Significantly fewer patients in the safinamide group, compared to placebo, experienced depression as adverse event (p = 0.0444 after 6 months and p = 0.0057 after 2 years). CONCLUSION: The favorable effect of safinamide on mood may be explained by the improvement in wearing off and by its modulation of glutamatergic hyperactivity and reversible MAO-B inhibition. Prospective studies are warranted to investigate this potential benefit. IOS Press 2017-11-01 /pmc/articles/PMC5676861/ /pubmed/28777756 http://dx.doi.org/10.3233/JPD-171143 Text en © 2017 – IOS Press and the authors. All rights reserved https://creativecommons.org/licenses/by-nc/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial (CC BY-NC 4.0) License (https://creativecommons.org/licenses/by-nc/4.0/) , which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Report
Cattaneo, Carlo
Müller, Thomas
Bonizzoni, Erminio
Lazzeri, Gabriele
Kottakis, Ioannis
Keywood, Charlotte
Long-Term Effects of Safinamide on Mood Fluctuations in Parkinson’s Disease
title Long-Term Effects of Safinamide on Mood Fluctuations in Parkinson’s Disease
title_full Long-Term Effects of Safinamide on Mood Fluctuations in Parkinson’s Disease
title_fullStr Long-Term Effects of Safinamide on Mood Fluctuations in Parkinson’s Disease
title_full_unstemmed Long-Term Effects of Safinamide on Mood Fluctuations in Parkinson’s Disease
title_short Long-Term Effects of Safinamide on Mood Fluctuations in Parkinson’s Disease
title_sort long-term effects of safinamide on mood fluctuations in parkinson’s disease
topic Research Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5676861/
https://www.ncbi.nlm.nih.gov/pubmed/28777756
http://dx.doi.org/10.3233/JPD-171143
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