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Effects of Ginkgo biloba in dementia: systematic review and meta-analysis

BACKGROUND: The benefit of Ginkgo biloba has been discussed controversially. The aim of this review was to assess the effects of Ginkgo biloba in Alzheimer's disease as well as vascular and mixed dementia covering a variety of outcome domains. METHODS: We searched MEDLINE, EMBASE, the Cochrane...

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Autores principales: Weinmann, Stefan, Roll, Stephanie, Schwarzbach, Christoph, Vauth, Christoph, Willich, Stefan N
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2846949/
https://www.ncbi.nlm.nih.gov/pubmed/20236541
http://dx.doi.org/10.1186/1471-2318-10-14
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author Weinmann, Stefan
Roll, Stephanie
Schwarzbach, Christoph
Vauth, Christoph
Willich, Stefan N
author_facet Weinmann, Stefan
Roll, Stephanie
Schwarzbach, Christoph
Vauth, Christoph
Willich, Stefan N
author_sort Weinmann, Stefan
collection PubMed
description BACKGROUND: The benefit of Ginkgo biloba has been discussed controversially. The aim of this review was to assess the effects of Ginkgo biloba in Alzheimer's disease as well as vascular and mixed dementia covering a variety of outcome domains. METHODS: We searched MEDLINE, EMBASE, the Cochrane databases, CINAHL and PsycINFO for controlled trials of ginkgo for Alzheimer's, vascular or mixed dementia. Studies had to be of a minimum of 12 weeks duration with at least ten participants per group. Clinical characteristics and outcomes were extracted. Meta-analysis results were expressed as risk ratios or standardized mean differences (SMD) in scores. RESULTS: Nine trials using the standardized extract EGb761(® )met our inclusion criteria. Trials were of 12 to 52 weeks duration and included 2372 patients in total. In the meta-analysis, the SMDs in change scores for cognition were in favor of ginkgo compared to placebo (-0.58, 95% confidence interval [CI] -1.14; -0.01, p = 0.04), but did not show a statistically significant difference from placebo for activities in daily living (ADLs) (SMD = -0.32, 95% CI -0.66; 0.03, p = 0.08). Heterogeneity among studies was high. For the Alzheimer subgroup, the SMDs for ADLs and cognition outcomes were larger than for the whole group of dementias with statistical superiority for ginkgo also for ADL outcomes (SMD = -0.44, 95% CI -0.77; -0.12, p = 0.008). Drop-out rates and side effects did not differ between ginkgo and placebo. No consistent results were available for quality of life and neuropsychiatric symptoms, possibly due to the heterogeneity of the study populations. CONCLUSIONS: Ginkgo biloba appears more effective than placebo. Effect sizes were moderate, while clinical relevance is, similar to other dementia drugs, difficult to determine.
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spelling pubmed-28469492010-03-30 Effects of Ginkgo biloba in dementia: systematic review and meta-analysis Weinmann, Stefan Roll, Stephanie Schwarzbach, Christoph Vauth, Christoph Willich, Stefan N BMC Geriatr Research article BACKGROUND: The benefit of Ginkgo biloba has been discussed controversially. The aim of this review was to assess the effects of Ginkgo biloba in Alzheimer's disease as well as vascular and mixed dementia covering a variety of outcome domains. METHODS: We searched MEDLINE, EMBASE, the Cochrane databases, CINAHL and PsycINFO for controlled trials of ginkgo for Alzheimer's, vascular or mixed dementia. Studies had to be of a minimum of 12 weeks duration with at least ten participants per group. Clinical characteristics and outcomes were extracted. Meta-analysis results were expressed as risk ratios or standardized mean differences (SMD) in scores. RESULTS: Nine trials using the standardized extract EGb761(® )met our inclusion criteria. Trials were of 12 to 52 weeks duration and included 2372 patients in total. In the meta-analysis, the SMDs in change scores for cognition were in favor of ginkgo compared to placebo (-0.58, 95% confidence interval [CI] -1.14; -0.01, p = 0.04), but did not show a statistically significant difference from placebo for activities in daily living (ADLs) (SMD = -0.32, 95% CI -0.66; 0.03, p = 0.08). Heterogeneity among studies was high. For the Alzheimer subgroup, the SMDs for ADLs and cognition outcomes were larger than for the whole group of dementias with statistical superiority for ginkgo also for ADL outcomes (SMD = -0.44, 95% CI -0.77; -0.12, p = 0.008). Drop-out rates and side effects did not differ between ginkgo and placebo. No consistent results were available for quality of life and neuropsychiatric symptoms, possibly due to the heterogeneity of the study populations. CONCLUSIONS: Ginkgo biloba appears more effective than placebo. Effect sizes were moderate, while clinical relevance is, similar to other dementia drugs, difficult to determine. BioMed Central 2010-03-17 /pmc/articles/PMC2846949/ /pubmed/20236541 http://dx.doi.org/10.1186/1471-2318-10-14 Text en Copyright ©2010 Weinmann et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research article
Weinmann, Stefan
Roll, Stephanie
Schwarzbach, Christoph
Vauth, Christoph
Willich, Stefan N
Effects of Ginkgo biloba in dementia: systematic review and meta-analysis
title Effects of Ginkgo biloba in dementia: systematic review and meta-analysis
title_full Effects of Ginkgo biloba in dementia: systematic review and meta-analysis
title_fullStr Effects of Ginkgo biloba in dementia: systematic review and meta-analysis
title_full_unstemmed Effects of Ginkgo biloba in dementia: systematic review and meta-analysis
title_short Effects of Ginkgo biloba in dementia: systematic review and meta-analysis
title_sort effects of ginkgo biloba in dementia: systematic review and meta-analysis
topic Research article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2846949/
https://www.ncbi.nlm.nih.gov/pubmed/20236541
http://dx.doi.org/10.1186/1471-2318-10-14
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