Mcjm. Van Dongen et al., The efficacy of ginkgo for elderly people with dementia and age-associatedmemory impairment: New results of a randomized clinical trial, J AM GER SO, 48(10), 2000, pp. 1183-1194
Citations number
62
Categorie Soggetti
Public Health & Health Care Science","General & Internal Medicine
OBJECTIVES: To evaluate the efficacy, the dose-dependence, and the durabili
ty of the effect of the ginkgo biloba special extract EGb 761 (ginkgo) in o
lder people with dementia or age-associated memory impairment.
DESIGN: A 24-week, randomized, double-blind, placebo-controlled, parallel-g
roup, multicenter trial.
SETTING: Homes for the elderly in the southern part of the Netherlands.
PARTICIPANTS: Older persons with dementia (either Alzheimer's dementia or v
ascular dementia; mild to moderate degree) or age-associated memory impairm
ent (AAMI). 214 Participants were recruited from 39 homes for the elderly.
INTERVENTION: The participants were allocated randomly to treatment with EG
b 761 (2 tablets per day, total dosage either 240 (high dose) or 160 (usual
dose) mg/day) or placebo (0 mg/d). The total intervention period was 24 we
eks. After 12 weeks of treatment, the initial ginkgo users were randomized
once again to either continued ginkgo treatment or placebo treatment. Initi
al placebo use was prolonged after 12 weeks.
MEASUREMENTS: Outcomes were assessed after 12 and 24 weeks of intervention.
Outcome measures included neuropsychological testing (trail-making speed (
NAI-ZVT-G), digit memory span (NAI-ZN-G), and verbal learning (NAI-WL)), cl
inical assessment (presence and severity of geriatric symptoms (SCAG), depr
essive mood (GDS), self-perceived health and memory status (report marks)),
and behavioral assessment (self-reported level of instrumental daily life
activities).
RESULTS: An intention-to-treat analysis showed no effect on each of the out
come measures for participants who were assigned to ginkgo (n = 79) compare
d with placebo (n = 44) for the entire 24-week period. After 12 weeks of tr
eatment, the combined high dose and usual dose ginkgo groups (n = 166) perf
ormed slightly better with regard to self-reported activities of daily life
but slightly worse with regard to self-perceived health status compared wi
th the placebo group (n = 48). No beneficial effects of a higher dose or a
prolonged duration of ginkgo treatment were found. We could not detect any
subgroup that benefited from ginkgo. Ginkgo use was also not associated wit
h the occurrence of (serious) adverse events.
CONCLUSIONS: The results of our trial suggest that ginkgo is not effective
as a treatment for older people with mild to moderate dementia or age-assoc
iated memory impairment. Our results contrast sharply with those of previou
s ginkgo trials.