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美金刚与胆碱酯酶抑制剂联合治疗阿尔茨海默病:一项系统评价。

Memantine and cholinesterase inhibitor combination therapy for Alzheimer's disease: a systematic review.

作者信息

Farrimond Lucy E, Roberts Emmert, McShane Rupert

机构信息

University of Oxford Medical School, Oxford, UK.

出版信息

BMJ Open. 2012 Jun 11;2(3). doi: 10.1136/bmjopen-2012-000917. Print 2012.

Abstract

BACKGROUND

Memantine is licensed for moderate-to-severe Alzheimer's disease (AD). National Institute for Clinical Excellence (NICE) guidance does not recommend the use of memantine in combination with cholinesterase inhibitors (acetylcholinesterase inhibitor (AChEI)). The underpinning meta-analysis was disputed by the manufacturer.

OBJECTIVES

To compare the efficacy of AChEI monotherapy with combination memantine and AChEI therapy in patients with moderate-to-severe AD and to examine the impact of including unpublished data on the results.

DESIGN

Systematic review and meta-analysis of randomised controlled trials.

DATA SOURCES

The Cochrane Dementia Group trial register, ALOIS, searched for the last time on 3 May 2011.

DATA SYNTHESIS

Data from four domains (clinical global, cognition, function, behaviour and mood) were pooled. Sensitivity analyses examined the impact on the NICE-commissioned meta-analysis of restricting data to patients with moderate-to-severe AD and of including an unpublished trial of an extended release preparation of memantine.

RESULTS

Pooled data from the trials, which were included in the NICE-commissioned meta-analysis but which were restricted to moderate-to-severe AD only, showed a small effect of combination therapy on cognition (standardised mean difference (SMD)=-0.29, 95% CI -0.45 to -0.14). Adding data from an unpublished trial of an extended release memantine (total three trials, 1317 participants) showed a small benefit of combination therapy on global scores (SMD=-0.20, 95% CI -0.31 to -0.09), cognition (SMD=-0.25, 95% CI -0.36 to -0.14) and behaviour and mood (SMD=-0.17, 95% CI -0.32 to -0.03) but not on function (SMD=-0.04, 95% CI -0.21 to 0.13) at 6 months. No clinical data have been reported from a 1-year trial, although this found 'no significant benefit' on any clinical measures at 1 year.

CONCLUSIONS

These results suggest that there may be a small benefit at 6 months of adding memantine to AChEIs. However, the impact on clinical global impression depends on exactly which studies are included, and there is no benefit on function, so its clinical relevance is not robustly demonstrated. Currently available information from randomised controlled trails indicates no benefit of combination therapy over monotherapy at 1 year. Legislation on the form and content of registry posted results is needed in Europe.

摘要

背景

美金刚被批准用于中重度阿尔茨海默病(AD)。英国国家卫生与临床优化研究所(NICE)指南不推荐美金刚与胆碱酯酶抑制剂(乙酰胆碱酯酶抑制剂(AChEI))联合使用。基础荟萃分析受到制造商的质疑。

目的

比较AChEI单药治疗与美金刚联合AChEI治疗对中重度AD患者的疗效,并研究纳入未发表数据对结果的影响。

设计

随机对照试验的系统评价和荟萃分析。

数据来源

Cochrane痴呆症小组试验注册库ALOIS,于2011年5月3日最后一次检索。

数据综合

汇总了来自四个领域(临床总体、认知、功能、行为和情绪)的数据。敏感性分析研究了将数据限制于中重度AD患者以及纳入一项美金刚缓释制剂未发表试验对NICE委托进行的荟萃分析的影响。

结果

纳入NICE委托进行的荟萃分析但仅限制于中重度AD患者的试验汇总数据显示,联合治疗对认知有小的影响(标准化均数差(SMD)=-0.29,95%可信区间-0.45至-0.14)。加入一项美金刚缓释制剂未发表试验的数据(共三项试验,1317名参与者)显示,联合治疗在6个月时对总体评分(SMD=-0.20,95%可信区间-0.31至-0.09)、认知(SMD=-0.25,95%可信区间-0.36至-0.14)以及行为和情绪(SMD=-0.17,95%可信区间-0.32至-0.03)有小的益处,但对功能无益处(SMD=-0.04,95%可信区间-0.21至0.13)。一项1年试验未报告临床数据,尽管该试验发现在1年时对任何临床指标均“无显著益处”。

结论

这些结果表明,在AChEIs基础上加用美金刚在6个月时可能有小的益处。然而,对临床总体印象的影响取决于具体纳入哪些研究,且对功能无益处,因此其临床相关性未得到有力证明。目前来自随机对照试验的现有信息表明,联合治疗在1年时并不优于单药治疗。欧洲需要制定关于注册公布结果的形式和内容的法规。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7971/3378937/fd7fe69818c1/bmjopen-2012-000917fig1.jpg

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