van Dongen M C, van Rossum E, Kessels A G, Sielhorst H J, Knipschild P G
Department of Epidemiology, Maastricht University, The Netherlands.
J Am Geriatr Soc. 2000 Oct;48(10):1183-94. doi: 10.1111/j.1532-5415.2000.tb02589.x.
To evaluate the efficacy, the dose-dependence, and the durability of the effect of the ginkgo biloba special extract EGb 761 (ginkgo) in older people with dementia or age-associated memory impairment.
A 24-week, randomized, double-blind, placebo-controlled, parallel-group, multicenter trial.
Homes for the elderly in the southern part of the Netherlands.
Older persons with dementia (either Alzheimer's dementia or vascular dementia; mild to moderate degree) or age-associated memory impairment (AAMI). 214 Participants were recruited from 39 homes for the elderly.
The participants were allocated randomly to treatment with EGb 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 weeks. After 12 weeks of treatment, the initial ginkgo users were randomized once again to either continued ginkgo treatment or placebo treatment. Initial placebo use was prolonged after 12 weeks.
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)), clinical assessment (presence and severity of geriatric symptoms (SCAG), depressive mood (GDS), self-perceived health and memory status (report marks)), and behavioral assessment (self-reported level of instrumental daily life activities).
An intention-to-treat analysis showed no effect on each of the outcome measures for participants who were assigned to ginkgo (n = 79) compared with placebo (n = 44) for the entire 24-week period. After 12 weeks of treatment, the combined high dose and usual dose ginkgo groups (n = 166) performed slightly better with regard to self-reported activities of daily life but slightly worse with regard to self-perceived health status compared with 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 with the occurrence of (serious) adverse events.
The results of our trial suggest that ginkgo is not effective as a treatment for older people with mild to moderate dementia or age-associated memory impairment. Our results contrast sharply with those of previous ginkgo trials.
评估银杏叶特殊提取物EGb 761(银杏)对患有痴呆症或年龄相关性记忆障碍的老年人的疗效、剂量依赖性及效果的持久性。
一项为期24周的随机、双盲、安慰剂对照、平行组多中心试验。
荷兰南部的养老院。
患有痴呆症(阿尔茨海默病性痴呆或血管性痴呆;轻度至中度)或年龄相关性记忆障碍(AAMI)的老年人。从39家养老院招募了214名参与者。
参与者被随机分配接受EGb 治疗(每天2片,总剂量为240(高剂量)或160(常规剂量)mg/天)或安慰剂(0mg/d)。总干预期为24周。治疗12周后,最初服用银杏的参与者再次随机分为继续接受银杏治疗或安慰剂治疗。最初服用安慰剂的参与者在12周后延长服用时间。
在干预12周和24周后评估结果。结果指标包括神经心理学测试(连线速度(NAI-ZVT-G)、数字记忆广度(NAI-ZN-G)和语言学习(NAI-WL))、临床评估(老年症状的存在和严重程度(SCAG)、抑郁情绪(GDS)、自我感知的健康和记忆状况(报告评分))以及行为评估(自我报告的工具性日常生活活动水平)。
意向性分析显示,在整个24周期间,与安慰剂组(n = 44)相比,服用银杏组(n = 79)的参与者在各项结果指标上均无效果。治疗12周后,与安慰剂组(n = 48)相比,高剂量和常规剂量银杏联合组(n = 166)在自我报告的日常生活活动方面表现略好,但在自我感知的健康状况方面表现略差。未发现更高剂量或更长疗程的银杏治疗有有益效果。我们未检测到任何从银杏治疗中获益的亚组。服用银杏也与(严重)不良事件的发生无关。
我们试验的结果表明,银杏对患有轻度至中度痴呆症或年龄相关性记忆障碍的老年人无效。我们的结果与之前银杏试验的结果形成鲜明对比。