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Treatment Options for Dementia with Lewy Bodies: A Network Meta-Analysis of Randomised Control Trials

INTRODUCTION: Dementia with Lewy bodies (DLB) is the third most common type of dementia after Alzheimer’s disease (AD) and vascular dementia. Treatment is targeted at specific disease manifestations/symptoms. While donepezil is approved for the treatment of DLB in Japan, to date no other treatment h...

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Autores principales: Tahami Monfared, Amir A., Desai, Mitesh, Hughes, Robert, Lucherini, Stefano, Yi, Yunni, Perry, Richard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Healthcare 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7606367/
https://www.ncbi.nlm.nih.gov/pubmed/32495063
http://dx.doi.org/10.1007/s40120-020-00198-0
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author Tahami Monfared, Amir A.
Desai, Mitesh
Hughes, Robert
Lucherini, Stefano
Yi, Yunni
Perry, Richard
author_facet Tahami Monfared, Amir A.
Desai, Mitesh
Hughes, Robert
Lucherini, Stefano
Yi, Yunni
Perry, Richard
author_sort Tahami Monfared, Amir A.
collection PubMed
description INTRODUCTION: Dementia with Lewy bodies (DLB) is the third most common type of dementia after Alzheimer’s disease (AD) and vascular dementia. Treatment is targeted at specific disease manifestations/symptoms. While donepezil is approved for the treatment of DLB in Japan, to date no other treatment has been approved for this indication anywhere in the world. Notwithstanding, many of the medications that are approved for AD are widely used in the treatment of DLB with varying degrees of success. Consequently, clinical evidence is limited, and there is a need to understand the comparative efficacy and safety of currently used therapies for DLB. The aim of this study was to conduct a network meta-analysis (NMA) to evaluate the outcomes of the available treatment options based on currently used trial endpoints. METHODS: Using data from a previously published systematic review, we conducted an NMA to investigate the efficacy and safety of treatments in patients with DLB. Networks were based on change from baseline of efficacy endpoints (Mini-Mental State Examination; Neuropsychiatric Inventory; Unified Parkinson’s Disease Rating Scale) and rate of safety events (overall adverse events [AEs]; discontinuations; discontinuations due to AEs; psychiatric events). RESULTS: Focused around a common treatment option of placebo, the NMA comprised studies on donepezil, rivastigmine, memantine and quetiapine. Donepezil 3 mg, 5 mg and 10 mg doses were compared against each other and placebo. Overall, donepezil consistently performed better than the alternative treatments when compared to placebo for all efficacy and safety endpoints. However, the small sample size and/or heterogeneity of the studies led to uncertainty, resulting in no statistically significant differences favouring any treatment above another or placebo. CONCLUSION: Despite the lack of statistical significance, when assessing the efficacy and safety outcomes for each drug in the evidence network, donepezil appeared to have a more favourable overall benefit/risk profile for patients with DLB. Further comparative trials are required to improve understanding of the true difference between existing and potential future treatment options. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s40120-020-00198-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-76063672020-11-10 Treatment Options for Dementia with Lewy Bodies: A Network Meta-Analysis of Randomised Control Trials Tahami Monfared, Amir A. Desai, Mitesh Hughes, Robert Lucherini, Stefano Yi, Yunni Perry, Richard Neurol Ther Original Research INTRODUCTION: Dementia with Lewy bodies (DLB) is the third most common type of dementia after Alzheimer’s disease (AD) and vascular dementia. Treatment is targeted at specific disease manifestations/symptoms. While donepezil is approved for the treatment of DLB in Japan, to date no other treatment has been approved for this indication anywhere in the world. Notwithstanding, many of the medications that are approved for AD are widely used in the treatment of DLB with varying degrees of success. Consequently, clinical evidence is limited, and there is a need to understand the comparative efficacy and safety of currently used therapies for DLB. The aim of this study was to conduct a network meta-analysis (NMA) to evaluate the outcomes of the available treatment options based on currently used trial endpoints. METHODS: Using data from a previously published systematic review, we conducted an NMA to investigate the efficacy and safety of treatments in patients with DLB. Networks were based on change from baseline of efficacy endpoints (Mini-Mental State Examination; Neuropsychiatric Inventory; Unified Parkinson’s Disease Rating Scale) and rate of safety events (overall adverse events [AEs]; discontinuations; discontinuations due to AEs; psychiatric events). RESULTS: Focused around a common treatment option of placebo, the NMA comprised studies on donepezil, rivastigmine, memantine and quetiapine. Donepezil 3 mg, 5 mg and 10 mg doses were compared against each other and placebo. Overall, donepezil consistently performed better than the alternative treatments when compared to placebo for all efficacy and safety endpoints. However, the small sample size and/or heterogeneity of the studies led to uncertainty, resulting in no statistically significant differences favouring any treatment above another or placebo. CONCLUSION: Despite the lack of statistical significance, when assessing the efficacy and safety outcomes for each drug in the evidence network, donepezil appeared to have a more favourable overall benefit/risk profile for patients with DLB. Further comparative trials are required to improve understanding of the true difference between existing and potential future treatment options. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s40120-020-00198-0) contains supplementary material, which is available to authorized users. Springer Healthcare 2020-06-03 /pmc/articles/PMC7606367/ /pubmed/32495063 http://dx.doi.org/10.1007/s40120-020-00198-0 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/This article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Original Research
Tahami Monfared, Amir A.
Desai, Mitesh
Hughes, Robert
Lucherini, Stefano
Yi, Yunni
Perry, Richard
Treatment Options for Dementia with Lewy Bodies: A Network Meta-Analysis of Randomised Control Trials
title Treatment Options for Dementia with Lewy Bodies: A Network Meta-Analysis of Randomised Control Trials
title_full Treatment Options for Dementia with Lewy Bodies: A Network Meta-Analysis of Randomised Control Trials
title_fullStr Treatment Options for Dementia with Lewy Bodies: A Network Meta-Analysis of Randomised Control Trials
title_full_unstemmed Treatment Options for Dementia with Lewy Bodies: A Network Meta-Analysis of Randomised Control Trials
title_short Treatment Options for Dementia with Lewy Bodies: A Network Meta-Analysis of Randomised Control Trials
title_sort treatment options for dementia with lewy bodies: a network meta-analysis of randomised control trials
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7606367/
https://www.ncbi.nlm.nih.gov/pubmed/32495063
http://dx.doi.org/10.1007/s40120-020-00198-0
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