Suppr超能文献

盐酸维纳克林治疗阿尔茨海默病的有效性和安全性。一项双盲、安慰剂对照研究。门坦研究组。

Effectiveness and safety of velnacrine for the treatment of Alzheimer's disease. A double-blind, placebo-controlled study. Mentane Study Group.

作者信息

Antuono P G

机构信息

Neurology Department, Medical College of Wisconsin, Milwaukee, USA.

出版信息

Arch Intern Med. 1995 Sep 11;155(16):1766-72.

PMID:7654110
Abstract

BACKGROUND

Alzheimer's disease is characterized by cognitive and behavioral disturbances that are mediated in part by cholinergic brain deficits.

OBJECTIVE

To evaluate the long-term effectiveness and safety of an investigational cholinesterase inhibitor, that is, velnacrine maleate, in treating patients with clinically probable Alzheimer's disease (according to the criteria of the National Institute of Neurological Disorders and Stroke [Washington, DC]-Alzheimer Disease and Related Disorders Association [Chicago, Ill]).

METHODS

This was a double-blind, placebo-controlled study. After a single-blind washout period, patients were randomized to receive placebo (n = 152), velnacrine maleate, 150 mg/d (n = 149), or velnacrine maleate, 225 mg/d (n = 148) for 24 weeks. Primary end points were cognitive behavior and memory components of the Alzheimer's Disease Assessment Scale and the Clinical Global Impression of Change scale. Secondary end points were caregiver-rated scales.

RESULTS

The scores for the cognitive behavior and memory components of the Alzheimer's Disease Assessment Scale deteriorated in the placebo-treated group (P < .05) but not in the velnacrine-treated groups. Between-group comparisons favored velnacrine maleate, 225 mg over 150 mg (P < .05). Findings were similar for the Clinical Global Impression of Change scale and three of the four caregiver-rated scales. Treatment-related adverse clinical events occurred in 36%, 28%, and 30% of patients in the groups that received placebo, velnacrine maleate (150 mg), and velnacrine maleate (225 mg), respectively. The most common adverse clinical event was diarrhea, which rarely interrupted therapy. Treatment was stopped because of reversible abnormal liver function test results (five or more times the upper limits of normal) in 3%, 30%, and 24% of the patients who received placebo, velnacrine maleate (150 mg), and velnacrine maleate (225 mg), respectively.

CONCLUSIONS

Velnacrine produces modest but significant benefits in patients with Alzheimer's disease. Velnacrine maleate (225 mg) is more effective than 150 mg of velnacrine. Both dosages have acceptable safety profiles.

摘要

背景

阿尔茨海默病的特征是认知和行为障碍,部分由胆碱能脑功能缺陷介导。

目的

评估一种研究性胆碱酯酶抑制剂,即马来酸韦那克林,治疗临床可能的阿尔茨海默病患者(根据美国国立神经疾病和中风研究所[华盛顿特区]-阿尔茨海默病及相关疾病协会[伊利诺伊州芝加哥]的标准)的长期有效性和安全性。

方法

这是一项双盲、安慰剂对照研究。经过单盲洗脱期后,患者被随机分配接受安慰剂(n = 152)、马来酸韦那克林150 mg/d(n = 149)或马来酸韦那克林225 mg/d(n = 148),为期24周。主要终点是阿尔茨海默病评估量表的认知行为和记忆部分以及临床总体印象变化量表。次要终点是照料者评定量表。

结果

安慰剂治疗组阿尔茨海默病评估量表的认知行为和记忆部分得分恶化(P <.05),而韦那克林治疗组未恶化。组间比较显示,225 mg马来酸韦那克林比150 mg更具优势(P <.05)。临床总体印象变化量表以及四个照料者评定量表中的三个量表的结果相似。接受安慰剂、马来酸韦那克林(150 mg)和马来酸韦那克林(225 mg)治疗的患者中,与治疗相关的不良临床事件发生率分别为36%、28%和30%。最常见的不良临床事件是腹泻,很少导致治疗中断。接受安慰剂、马来酸韦那克林(150 mg)和马来酸韦那克林(225 mg)治疗的患者中,分别有3%、30%和24%因可逆性肝功能检查结果异常(超过正常上限五倍或更多)而停止治疗。

结论

韦那克林对阿尔茨海默病患者有适度但显著的益处。225 mg马来酸韦那克林比150 mg韦那克林更有效。两种剂量均具有可接受的安全性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验