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奥氮平不能改善轻至中度阿尔茨海默病痴呆的非激越性和非精神病性患者的认知功能。

Olanzapine does not enhance cognition in non-agitated and non-psychotic patients with mild to moderate Alzheimer's dementia.

作者信息

Kennedy John, Deberdt Walter, Siegal Alan, Micca Joseph, Degenhardt Elisabeth, Ahl Jonna, Meyers Adam, Kaiser Christopher, Baker Robert W

机构信息

University of Alberta and Chinook Regional Health System, Alberta, Canada.

出版信息

Int J Geriatr Psychiatry. 2005 Nov;20(11):1020-7. doi: 10.1002/gps.1397.

Abstract

OBJECTIVE

This was an exploratory study of olanzapine as potential treatment for improvement in cognition in patients with Alzheimer's disease without prominent psychobehavioral symptoms.

METHODS

Non-psychotic/non-agitated patients (n = 268) with Alzheimer's disease, who had baseline Mini-Mental State Examination (MMSE) scores of 14-26 were randomized to treatment with olanzapine (2.5 to 7.5 mg/d) or placebo for 26 weeks. The primary objectives were to determine if treatment with olanzapine improved cognition as indexed by the Alzheimer's disease Assessment Scale for Cognition (ADAS-Cog) and the Clinician's Interview-Based Impression of Change (CIBIC) after 26 weeks of therapy.

RESULTS

Patients treated with olanzapine vs placebo experienced significant worsening ADAS-Cog scores at weeks 12 (p = 0.03) and 26 (p = 0.004). Changes in CIBIC scores were not significantly different between treatment groups at either assessment. A post hoc analysis revealed that olanzapine-treated patients with more cognitive impairment at baseline (MMSE scores of 14-18) (n = 35) experienced significantly greater deterioration in ADAS-Cog performance than patients in the placebo group (n = 24; p < 0.001); whereas in patients with less cognitive impairment (n = 78, baseline MMSE scores of 23-26) between-group ADAS-Cog changes were not significant.

CONCLUSIONS

In this 26-week study non-psychotic/non-agitated patients with Alzheimer's disease treated with olanzapine experienced significant worsening of cognition as compared to placebo.

摘要

目的

本研究旨在探索奥氮平对无明显精神行为症状的阿尔茨海默病患者认知功能改善的潜在治疗作用。

方法

将268例患有阿尔茨海默病的非精神病性/非激越性患者随机分为两组,这些患者的简易精神状态检查表(MMSE)基线评分在14至26分之间,一组接受奥氮平治疗(2.5至7.5毫克/天),另一组接受安慰剂治疗,为期26周。主要目的是确定经过26周治疗后,以阿尔茨海默病认知评估量表(ADAS-Cog)和临床医生基于访谈的疗效印象(CIBIC)为指标,奥氮平治疗是否能改善认知功能。

结果

与安慰剂组相比,接受奥氮平治疗的患者在第12周(p = 0.03)和第26周(p = 0.004)时ADAS-Cog评分显著恶化。在两次评估中,治疗组之间的CIBIC评分变化无显著差异。事后分析显示,基线时认知损害更严重(MMSE评分为14 - 18分)的奥氮平治疗患者(n = 35),其ADAS-Cog表现的恶化程度显著大于安慰剂组患者(n = 24;p < 0.001);而在认知损害较轻的患者(n = 78,基线MMSE评分为23 - 26分)中,组间ADAS-Cog变化不显著。

结论

在这项为期26周的研究中,与安慰剂相比,接受奥氮平治疗的无明显精神行为症状的阿尔茨海默病患者认知功能显著恶化。

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