Meta-Analysis of Randomized Controlled Trials on the Efficacy and Safety of Donepezil, Galantamine, Rivastigmine, and Memantine for the Treatment of Alzheimer’s Disease

加兰他明 竞争对手 多奈哌齐 美金刚 医学 随机对照试验 药理学 痴呆 心理学 疾病 内科学
作者
Dandan Li,Yahong Zhang,Wei Zhang,Pu Zhao
出处
期刊:Frontiers in Neuroscience [Frontiers Media]
卷期号:13: 472-472 被引量:183
标识
DOI:10.3389/fnins.2019.00472
摘要

To study the impact of donepezil, rivastigmine, galantamine, and memantine on cognitive, functional, behavioral, global changes and adverse effects in patients with mild, moderate and severe Alzheimer’s disease (AD), we screened the literature published before September 2017 in the Pubmed, Embase, Cochrane library and Web of Science Electronic databases according to the inclusion criteria. Thirty-six studies were finally determined from 1560 preliminary screened articles. The AD Assessment Scale-cognitive Subscale (ADAS-cog), AD Cooperative Study-Activities of Daily Living (ADCS-ADL), Neuropsychiatric Inventory (NPI), and Clinician’s Interview-Based Impression of Change Plus Caregiver Input scale (CIBIC+) were used as valid endpoints. Of the 36 trials included, meta-analyses of these placebo-control trials showed that there were significant differences between the donepezil, rivastigmine and placebo groups using ADAS-cog, ADCS-ADL, and CIBIC+. Meta-analyses of these placebo-controlled trials showed that there were significant differences between the galantamine and placebo groups using ADAS-cog, ADCS-ADL, NPI, and CIBIC+. These observations suggest that memantine is beneficial for stabilizing or slowing the decline in ADAS-cog and ADCS-ADL19 changes in AD patients. However, there was no significant effect according to the ADCS-ADL23, NPI, and CIBIC+ tests, which indicated that memantine treatment has no significant effect on these cognitive aspects of AD patients. Different effects of donepezil, rivastigmine, galantamine, or memantine on AD were found in this study. According to the results, we conclude that galantamine is effective in treating all aspects of AD and is the first choice for the treatment of AD. However, due to limited data, we should consider additional data to obtain more stable results.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
科研通AI6.4应助zch采纳,获得10
刚刚
汉堡包应助能干的外套采纳,获得10
刚刚
孤独的小菜鸟完成签到,获得积分10
1秒前
2秒前
3秒前
FD发布了新的文献求助10
4秒前
干净丹彤发布了新的文献求助10
4秒前
4秒前
中科院一区选手完成签到,获得积分10
4秒前
柳惊完成签到,获得积分10
5秒前
努力熙熙发布了新的文献求助10
5秒前
5秒前
Belle完成签到,获得积分10
5秒前
泡芙发布了新的文献求助10
5秒前
奥本海草发布了新的文献求助10
6秒前
6秒前
小杰完成签到 ,获得积分10
7秒前
儒雅沛凝发布了新的文献求助10
7秒前
科目三应助木木同学采纳,获得20
7秒前
8秒前
8秒前
无极微光应助奥本海草采纳,获得20
9秒前
傅承静发布了新的文献求助10
9秒前
renwoxing完成签到,获得积分10
11秒前
渡春屿完成签到 ,获得积分10
11秒前
小鱼完成签到,获得积分10
11秒前
11秒前
一去应助主将从现采纳,获得30
12秒前
Ayue发布了新的文献求助10
12秒前
13秒前
13秒前
共享精神应助一期一会采纳,获得10
16秒前
Akim应助科研通管家采纳,获得10
16秒前
科研通AI2S应助科研通管家采纳,获得10
17秒前
汉堡包应助huntme采纳,获得10
17秒前
脑洞疼应助科研通管家采纳,获得10
17秒前
v0id应助科研通管家采纳,获得10
17秒前
laojiu发布了新的文献求助10
17秒前
Nole应助科研通管家采纳,获得10
17秒前
予辛完成签到,获得积分10
17秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
HYDROLYSE ACIDE DE QUELQUES DIOXASPIROCYCLANES 1314
Navigating Normative Orders. Interdisciplinary Perspectives 800
Essentials of Carbohydrate Chemistry and Biochemistry, 4th Edition 700
1 Peter and Christ's Descent to the Dead in Its Early Christian Reception 700
Organizational Behavior 510
Management and the Arts 510
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7742764
求助须知:如何正确求助?哪些是违规求助? 9290913
关于积分的说明 20205086
捐赠科研通 7321230
什么是DOI,文献DOI怎么找? 3307180
关于科研通互助平台的介绍 2459104
邀请新用户注册赠送积分活动 2317712