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Treatment Options for Dementia with Lewy Bodies: A Network Meta-Analysis of Randomised Control Trials
Amir A Tahami Monfared1,2, Mitesh Desai3, Robert Hughes3
1Eisai Inc., Woodcliff Lake, NJ, USA. amir_tahami@eisai.com.
Insights
This network meta-analysis suggests donepezil may offer the best benefit/risk profile for dementia with Lewy bodies (DLB) treatment, though further trials are needed to confirm efficacy and safety. The study compared donepezil, rivastigmine, memantine, and quetiapine.
Area of Science:
- Neurology
- Pharmacology
- Geriatrics
Background:
- Dementia with Lewy bodies (DLB) is the third most common dementia, with limited approved treatments globally.
- Current DLB management often involves off-label use of Alzheimer's disease medications, necessitating comparative efficacy and safety data.
- Donepezil is approved for DLB in Japan, but other treatments lack global approval for this indication.
Purpose of the Study:
- To conduct a network meta-analysis (NMA) evaluating the comparative efficacy and safety of available DLB treatment options.
- To assess outcomes based on standard clinical trial endpoints for DLB therapies.
Main Methods:
- A network meta-analysis (NMA) was performed using data from a prior systematic review.
- Efficacy endpoints included changes in Mini-Mental State Examination, Neuropsychiatric Inventory, and Unified Parkinson's Disease Rating Scale scores.
- Safety endpoints comprised overall adverse events, discontinuations, and psychiatric events.
Main Results:
- The NMA included studies on donepezil, rivastigmine, memantine, and quetiapine, with placebo as a common comparator.
- Donepezil demonstrated a trend towards better efficacy and safety compared to placebo across all assessed endpoints.
- However, small sample sizes and study heterogeneity resulted in no statistically significant differences between treatments or placebo.
Conclusions:
- Despite the lack of statistical significance, donepezil exhibited a potentially more favorable overall benefit/risk profile for DLB patients.
- Further comparative clinical trials are essential to elucidate definitive differences among existing and potential DLB treatments.
- Understanding the comparative effectiveness of DLB therapies remains crucial for optimizing patient care.
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.
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