The ASCOMALVA (Association between the Cholinesterase Inhibitor Donepezil and the Cholinergic Precursor Choline Alphoscerate in Alzheimer’s Disease) trial: interim results after two years of treatment.
Abstract
Cholinesterase inhibitors (ChE-Is) are used for symptomatic treatment of mild-to-moderate Alzheimer's disease (AD), but long-term effects of these compounds are mild and not always obvious. Preclinical studies have shown that combination of ChE-Is and the cholinergic precursor choline alphoscerate increases brain acetylcholine levels more effectively than single compounds alone. ASCOMALVA (Effect of association between a ChE-I and choline alphoscerate on cognitive deficits in AD associated with cerebrovascular injury) is a double-blind trial investigating if the ChE-I donepezil and choline alphoscerate in combination are more effective that donepezil alone. The trial has recruited AD patients suffering from ischemic brain damage documented by neuroimaging and has completed 2 years of observation in 113 patients of the 210 planned. Patients were randomly allotted to an active treatment group (donepezil + choline alphoscerate) or to a reference group (donepezil + placebo). Cognitive functions were assessed by the Mini-Mental State Evaluation and Alzheimer's Disease Assessment Scale Cognitive subscale. Daily activity was evaluated by the basic and instrumental activities of daily living tests. Behavioral symptoms were assessed by the Neuropsychiatric Inventory. Over the 24-month observation period, patients of the reference group showed a moderate time-dependent worsening in all the parameters investigated. Treatment with donepezil plus choline alphoscerate significantly slowed changes of the different items analyzed. These findings suggest that the combination of choline alphoscerate with a ChE-I may prolong/increase the effectiveness of cholinergic therapies in AD with concomitant ischemic cerebrovascular injury.
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The only double-blind multicenter trial of α-GPC reported that donepezil plus α-GPC might slow progressive cognitive decline compared with donepezil alone among 113 participants with Alzheimer disease with cerebrovascular injury after 12 and 24 months.
“The only double-blind multicenter trial of α-GPC reported that active treatment using the acetylcholinesterase inhibitors donepezil and α-GPC might slow progressive cognitive decline compared with donepezil treatment alone among 113 participants with Alzheimer disease with cerebrovascular injury after a 12- and 24-month observation period”
From Association of L-α Glycerylphosphorylcholine With Subsequent Stroke Risk After 10 Years (2021) · cites this paper as [6]
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References 24 · Cited by 50
- Authors
- Amenta, F., Carotenuto, A., Fasanaro, A. M., Rea, R., & Traini, E.
- Affiliations
- Università di Camerino (IT)
- Ospedale Antonio Cardarelli (IT)
- Corresponding author
- Amenta, Francesco
- Venue
- Journal of Alzheimer s Disease
- Publisher
- SAGE Publications
- Published
- 2014-09-02
- Volume
- 42
- Issue
- s3
- Pages
- S281-S288
- ISSN
- 1387-2877 (ISSN-L)
- 1875-8908
- OpenAlex
- W1626650988
- Cited by
- 50
- References
- 24
- Citations by year
- 2026: 4 · 2025: 13 · 2024: 9 · 2023: 4 · 2022: 5 · 2021: 2 · 2020: 4 · 2018: 3 · 2017: 1 · 2016: 3 · 2015: 2
- FWCI
- 1.45
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Alzheimer s Disease (publishedVersion)
- PubMed (publishedVersion)
- Unicam Scientific Publications (University of Camerino) (submittedVersion)
- Topics
- Health Sciences › Medicine › Pharmacology › Cholinesterase and Neurodegenerative Diseases
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
- Keywords
- Alzheimer's disease, donepezil
- MeSH terms
- Donepezil, Aged, Aged, 80 and over, Alzheimer Disease, Analysis of Variance, Double-Blind Method, Female, Glycerylphosphorylcholine, Humans, Indans, Longitudinal Studies, Male, Mental Status Schedule, Middle Aged, Piperidines, Severity of Illness Index, Antipsychotic Agents
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