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一项针对两剂银杏叶提取物治疗阿尔茨海默型痴呆症的随机、双盲、安慰剂对照试验。

A randomized, double-blind, placebo-controlled trial of two doses of Ginkgo biloba extract in dementia of the Alzheimer's type.

作者信息

Schneider Lon S, DeKosky Steven T, Farlow Martin R, Tariot Pierre N, Hoerr Robert, Kieser Meinhard

机构信息

Department of Psychiatry and the Behavioral Sciences, Keck School of Medicine, University of Southern California, Los Angeles, 90033, USA.

出版信息

Curr Alzheimer Res. 2005 Dec;2(5):541-51. doi: 10.2174/156720505774932287.

Abstract

CONTEXT

Previous studies of Ginkgo biloba extract (GbE) in patients with various forms of cognitive impairment or dementia have shown promising results.

OBJECTIVE

To determine the clinical efficacy of GbE in mild to moderate dementia of the Alzheimer type.

DESIGN

Randomized, placebo-controlled, double-blind, parallel-group, multicenter trial.

SETTING

Outpatient clinics of universities and private research centers specialized in dementia.

PATIENTS

513 outpatients with uncomplicated dementia of the Alzheimer's type scoring 10 to 24 on the Mini-Mental State Examination and less than 4 on the modified Hachinski Ischemic Score, free of other serious illnesses and not requiring continuous treatment with any psychoactive drug.

INTERVENTION

26-week treatment with GbE at daily doses of 120 mg or 240 mg or placebo.

MAIN OUTCOMES

Cognitive subscale of the Alzheimer's Disease Assessment Scale (ADAS-cog), Alzheimer's Disease Cooperative Study Clinical Global Impression of Change (ADCS-CGIC).

RESULTS

There were no significant between-group differences for the whole sample. There was little cognitive and functional decline of the placebo-treated patients, however. For a subgroup of patients with neuropsychiatric symptoms there was a greater decline of placebo-treated patients and significantly better cognitive performance and global assessment scores for the patients on GbE.

CONCLUSION

The trial did not show efficacy of GbE, however, the lack of decline of the placebo patients may have compromised the sensitivity of the trial to detect a treatment effect. Thus, the study remains inconclusive with respect to the efficacy of GbE.

摘要

背景

先前对银杏叶提取物(GbE)用于各种形式认知障碍或痴呆患者的研究已显示出有前景的结果。

目的

确定GbE在轻度至中度阿尔茨海默型痴呆中的临床疗效。

设计

随机、安慰剂对照、双盲、平行组、多中心试验。

地点

专门诊治痴呆的大学门诊和私立研究中心。

患者

513例患有单纯性阿尔茨海默型痴呆的门诊患者,简易精神状态检查表评分10至24分,改良哈金斯基缺血量表评分低于4分,无其他严重疾病且无需任何精神活性药物持续治疗。

干预

用每日剂量120毫克或240毫克的GbE或安慰剂进行26周治疗。

主要结局

阿尔茨海默病评估量表认知分量表(ADAS - cog)、阿尔茨海默病协作研究临床总体变化印象(ADCS - CGIC)。

结果

整个样本组间无显著差异。然而,安慰剂治疗组患者的认知和功能几乎没有下降。对于有神经精神症状的患者亚组,安慰剂治疗组患者的下降更大,而服用GbE的患者认知表现和总体评估得分显著更好。

结论

该试验未显示GbE的疗效,然而,安慰剂组患者缺乏下降可能损害了试验检测治疗效果的敏感性。因此,关于GbE的疗效,该研究尚无定论。

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