Anti-dementia drugs and changes in gait: a pre-post quasi-experimental pilot study.

Détails

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ID Serval
serval:BIB_C816878369B7
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Anti-dementia drugs and changes in gait: a pre-post quasi-experimental pilot study.
Périodique
BMC neurology
Auteur⸱e⸱s
Beauchet O., Launay C.P., Allali G., Watfa G., Gallouj K., Herrmann F.R., Annweiler C.
ISSN
1471-2377 (Electronic)
ISSN-L
1471-2377
Statut éditorial
Publié
Date de publication
21/11/2013
Peer-reviewed
Oui
Volume
13
Pages
184
Langue
anglais
Notes
Publication types: Clinical Trial ; Journal Article ; Research Support, Non-U.S. Gov't
Publication Status: epublish
Résumé
Anti-dementia drugs may improve gait performance. No comparison between acetylcholinesterase inhibitors (CEIs) and memantine-related changes in gait variability has been reported. The objectives of this study were to 1) quantify and compare the mean values and coefficients of variation (CoV) of stride time in demented patients with Alzheimer's disease and related disorders (ADRD) before and after the use of CEIs or memantine, and in age- and gender-matched controls patients with ADRD using no anti-dementia drugs; and 2) to determine whether changes in CoV of stride time differed between CEIs or memantine.
A total of 120 demented patients with mild-to-moderate ADRD were prospectively included in this pre-post quasi-experimental study with two intervention groups (43 patients taking CEIs, and 41 taking memantine) and a control group (36 age- and gender matched patients without any anti-dementia drugs). CoV of stride time and walking speed were measured with GAITRite® system while usual walking at steady state. Age, gender, number of drugs daily taken, use of psychoactive drugs, body mass index and time between the two visits were also recorded.
There was no difference between groups for the time between baseline and follow-up assessments (232.9 ± 103.7 days for patients without anti-dementia drugs, 220.0 ± 67.5 days for patients with CEIs, 186.7 ± 96.2 days for patients with memantine, P = 0.062). Patients with memantine had a lower (i.e., better) CoV of stride time at follow-up assessment compared to those with CEIs (4.2 ± 2.4% versus 5.8 ± 4.2%, P = 0.010). Patients with memantine had a greater decrease in CoV of stride time compared to those with CEIs (-1.90% versus 0.93%, P = 0.010) and mixed-effects linear regressions showed that this decrease was specifically explained by memantine (P = 0.028).
Our results showed that patients with ADRD and treated with memantine, but not those with CEIs, decreased their gait variability, and thus improved their gait safety (Trial registration number: NCT01315704).
Mots-clé
Aged, Aged, 80 and over, Alzheimer Disease/diagnosis, Alzheimer Disease/drug therapy, Cholinesterase Inhibitors/pharmacology, Cholinesterase Inhibitors/therapeutic use, Dementia/diagnosis, Dementia/drug therapy, Female, Follow-Up Studies, Gait/drug effects, Gait/physiology, Humans, Male, Memantine/pharmacology, Memantine/therapeutic use, Pilot Projects, Prospective Studies
Pubmed
Web of science
Open Access
Oui
Création de la notice
06/10/2023 8:19
Dernière modification de la notice
25/01/2024 7:44
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