Ginkgo biloba for Preventing Cognitive Decline in Older Adults A Randomized Trial

被引:213
|
作者
Snitz, Beth E. [2 ]
O'Meara, Ellen S. [4 ]
Carlson, Michelle C. [5 ]
Arnold, Alice M. [4 ]
Ives, Diane G. [3 ]
Rapp, Stephen R. [6 ]
Saxton, Judith [2 ]
Lopez, Oscar L. [2 ]
Dunn, Leslie O. [2 ]
Sink, Kaycee M. [7 ]
DeKosky, Steven T. [1 ,2 ]
机构
[1] Univ Virginia, Sch Med, Charlottesville, VA 22908 USA
[2] Univ Pittsburgh, Dept Neurol, Pittsburgh, PA 15260 USA
[3] Univ Pittsburgh, Dept Epidemiol, Pittsburgh, PA 15260 USA
[4] Univ Washington, Dept Biostat, Seattle, WA 98195 USA
[5] Johns Hopkins Med Inst, Dept Mental Hlth, Baltimore, MD 21205 USA
[6] Wake Forest Univ, Dept Psychiat & Behav Med, Winston Salem, NC 27109 USA
[7] Wake Forest Univ, Dept Internal Med Geriatr Gerontol, Sch Med, Winston Salem, NC 27109 USA
来源
关键词
EXTRACT EGB-761; BASE-LINE; MEMORY; IMPAIRMENT; DEMENTIA;
D O I
10.1001/jama.2009.1913
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context The herbal product Ginkgo biloba is taken frequently with the intention of improving cognitive health in aging. However, evidence from adequately powered clinical trials is lacking regarding its effect on long-term cognitive functioning. Objective To determine whether G biloba slows the rates of global or domain-specific cognitive decline in older adults. Design, Setting, and Participants The Ginkgo Evaluation of Memory ( GEM) study, a randomized, double-blind, placebo-controlled clinical trial of 3069 community-dwelling participants aged 72 to 96 years, conducted in 6 academic medical centers in the United States between 2000 and 2008, with a median follow-up of 6.1 years. Intervention Twice-daily dose of 120-mg extract of G biloba (n=1545) or identical-appearing placebo (n=1524). Main Outcome Measures Rates of change over time in the Modified Mini-Mental State Examination (3MSE), in the cognitive subscale of the Alzheimer Disease Assessment Scale (ADAS-Cog), and in neuropsychological domains of memory, attention, visual-spatial construction, language, and executive functions, based on sums of z scores of individual tests. Results Annual rates of decline in z scores did not differ between G biloba and placebo groups in any domains, including memory (0.043; 95% confidence interval [CI], 0.034-0.051 vs 0.041; 95% CI, 0.032-0.050), attention ( 0.043; 95% CI, 0.037-0.050 vs 0.048; 95% CI, 0.041-0.054), visuospatial abilities (0.107; 95% CI, 0.097-0.117 vs 0.118; 95% CI, 0.108-0.128), language (0.045; 95% CI, 0.037-0.054 vs 0.041; 95% CI, 0.033-0.048), and executive functions (0.092; 95% CI, 0.086-0.099 vs 0.089; 95% CI, 0.082-0.096). For the 3MSE and ADAS-Cog, rates of change varied by baseline cognitive status ( mild cognitive impairment), but there were no differences in rates of change between treatment groups ( for 3MSE, P=.71; for ADAS-Cog, P=.97). There was no significant effect modification of treatment on rate of decline by age, sex, race, education, APOE*E4 allele, or baseline mild cognitive impairment (P>.05). Conclusion Compared with placebo, the use of G biloba, 120 mg twice daily, did not result in less cognitive decline in older adults with normal cognition or with mild cognitive impairment. Trial Registration clinicaltrials.gov Identifier: NCT00010803 JAMA. 2009;302(24):2663-2670 www.jama.com
引用
收藏
页码:2663 / 2670
页数:8
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