Pharmacological Management of Apathy in Dementia.


Journal

CNS drugs
ISSN: 1179-1934
Titre abrégé: CNS Drugs
Pays: New Zealand
ID NLM: 9431220

Informations de publication

Date de publication:
02 2022
Historique:
accepted: 21 11 2021
pubmed: 11 1 2022
medline: 23 3 2022
entrez: 10 1 2022
Statut: ppublish

Résumé

Apathy is a highly prevalent symptom of dementia. Despite its association with faster cognitive and functional decline, decreased quality of life and increased mortality, no therapies are currently approved to treat apathy. The objective of this review was to summarize the drugs that have been studied for apathy treatment in patients with dementia (specifically Alzheimer's disease [AD], Huntington's disease [HD] and Parkinson's disease [PD] dementia; dementia with Lewy bodies [DLB]; vascular dementia [VaD]; and frontotemporal dementia [FTD]) based on their putative mechanisms of action. A search for relevant studies was performed using ClinicalTrials.gov and PubMed. Eligible studies were randomized controlled trials that were available in English and included at least one drug intervention and an apathy measure scale. A total of 52 studies that included patients with AD (n = 33 studies), PD (n = 5), HD (n = 1), DLB (n = 1), FTD (n = 3), VaD (n = 1), VaD and AD (n = 4), VaD and mixed dementia (n = 1), and AD, VaD and mixed dementia (n = 3) were eligible for inclusion. These studies showed that methylphenidate, olanzapine, cholinesterase inhibitors, choline alphoscerate, citalopram, memantine, and mibampator are the only beneficial drugs in AD-related apathy. For PD-related apathy, only methylphenidate, rotigotine and rivastigmine showed benefits. Regarding FTD- and DLB-related apathy, initial studies with agomelatine and rivastigmine showed benefits, respectively. As for HD- and only-VaD-related apathy, no drugs demonstrated benefits. With regards to mixed populations, memantine, galantamine and gingko biloba showed effects on apathy in the AD plus VaD populations and nimodipine in the VaD plus mixed dementia populations. Of the drugs with positive results, some are already prescribed to patients with dementia to target other symptoms, some have characteristics-such as medical contraindications (e.g., cardiovascular) and adverse effects (e.g., gastrointestinal disturbances)-that limit their clinical use and some require further study. Future studies should investigate apathy as a primary outcome, making use of appropriate sample sizes and study durations to ensure durability of results. There should also be a consensus on using scales with high test/retest and interrater reliabilities to limit the inconsistencies between clinical trials. In conclusion, there are currently no US FDA-approved drugs that target apathy in dementia, so there is an ongoing need for the development of such drugs.

Identifiants

pubmed: 35006557
doi: 10.1007/s40263-021-00883-0
pii: 10.1007/s40263-021-00883-0
doi:

Substances chimiques

Central Nervous System Stimulants 0
Dopamine Agonists 0
Serotonin Uptake Inhibitors 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

143-165

Informations de copyright

© 2022. The Author(s), under exclusive licence to Springer Nature Switzerland AG.

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Auteurs

Laiba Azhar (L)

Department of Pharmacology and Toxicology, University of Toronto, Toronto, ON, Canada.
Hurvitz Brain Sciences Research Program, Sunnybrook Research Institute, Toronto, ON, Canada.

Raphael W Kusumo (RW)

Hurvitz Brain Sciences Research Program, Sunnybrook Research Institute, Toronto, ON, Canada.

Giovanni Marotta (G)

Geriatric Medicine Division, Sunnybrook Health Sciences Centre, Toronto, ON, Canada.

Krista L Lanctôt (KL)

Department of Pharmacology and Toxicology, University of Toronto, Toronto, ON, Canada.
Hurvitz Brain Sciences Research Program, Sunnybrook Research Institute, Toronto, ON, Canada.
Department of Psychiatry, Sunnybrook Health Sciences Centre, Toronto, ON, Canada.
Department of Psychiatry, University of Toronto, Toronto, ON, Canada.

Nathan Herrmann (N)

Hurvitz Brain Sciences Research Program, Sunnybrook Research Institute, Toronto, ON, Canada. dr.nathan.herrmann@gmail.com.
Department of Psychiatry, Sunnybrook Health Sciences Centre, Toronto, ON, Canada. dr.nathan.herrmann@gmail.com.
Department of Psychiatry, University of Toronto, Toronto, ON, Canada. dr.nathan.herrmann@gmail.com.

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