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加兰他敏:对阿尔茨海默病患者的额外益处。

Galantamine: additional benefits to patients with Alzheimer's disease.

作者信息

Lilienfeld S, Parys W

机构信息

CNS Clinical Research, Janssen Research Foundation, Beerse, Belgium.

出版信息

Dement Geriatr Cogn Disord. 2000 Sep;11 Suppl 1:19-27. doi: 10.1159/000051228.

Abstract

Galantamine, a novel treatment for Alzheimer's disease (AD), has a dual mechanism of action, combining allosteric modulation of nicotinic acetylcholine receptors with reversible, competitive inhibition of acetylcholinesterase. In the Phase III clinical trial programme, over 3,000 patients with mild-to-moderate AD were enrolled in one of five randomized, controlled, double-blind studies. Using the Alzheimer's Disease Assessment Scale-cognitive subscale (ADAS-cog) to assess memory and other cognitive functions, galantamine was found to be significantly superior to placebo in all five studies at doses of 16, 24 and 32 mg/day. In all studies, galantamine-treated patients maintained their cognitive function, whereas the placebo-treated patients experienced a significant deterioration in ADAS-cog scores. The 32-mg/day dose was not associated with any additional cognitive benefit. Pooled data from two 6-month studies (n = 1,269), which were of identical design, show that the therapeutic benefits of galantamine are sustained for the duration of treatment. The treatment effect (galantamine-placebo difference on ADAS-cog) for the pooled data was approximately 4 points. Clinical benefit was seen in all levels of disease severity, with a 7-point advantage over placebo on ADAS-cog for patients with moderately severe disease. Galantamine was well tolerated, with most patients completing the 6-month studies. The long-term effects of galantamine have been evaluated in a 12-month study. Patients who completed one of the pivotal 6-month studies (n = 353) were entered into a 6-month open-label extension. Cognitive and daily function were maintained throughout the 12 months in patients who received galantamine 24 mg/day. This sustained level of benefit may reflect galantamine's dual effect on the cholinergic system. Data from a 5-month, placebo-controlled study have also shown that galantamine produces significant benefits on behavioural symptoms. The persistence and range of therapeutic effects produced by galantamine suggest that it may provide additional benefits for patients with AD.

摘要

加兰他敏是一种治疗阿尔茨海默病(AD)的新型药物,具有双重作用机制,它将烟碱型乙酰胆碱受体的变构调节与乙酰胆碱酯酶的可逆性竞争性抑制相结合。在III期临床试验项目中,超过3000例轻至中度AD患者被纳入五项随机、对照、双盲研究中的一项。使用阿尔茨海默病评估量表认知分量表(ADAS-cog)来评估记忆和其他认知功能,发现在所有五项研究中,加兰他敏在16、24和32毫克/天的剂量下均显著优于安慰剂。在所有研究中,接受加兰他敏治疗的患者维持了他们的认知功能,而接受安慰剂治疗的患者ADAS-cog评分出现了显著恶化。32毫克/天的剂量未显示出任何额外的认知益处。两项设计相同的6个月研究(n = 1269)的汇总数据表明,加兰他敏的治疗益处贯穿整个治疗期。汇总数据的治疗效果(加兰他敏与安慰剂在ADAS-cog上的差异)约为4分。在所有疾病严重程度水平上均观察到临床益处,中度严重疾病患者在ADAS-cog上比安慰剂有7分的优势。加兰他敏耐受性良好,大多数患者完成了6个月的研究。加兰他敏的长期效果已在一项12个月的研究中进行了评估。完成一项关键的6个月研究(n = 353)的患者进入了为期6个月的开放标签扩展研究。接受24毫克/天加兰他敏治疗的患者在整个12个月中认知和日常功能均得以维持。这种持续的益处水平可能反映了加兰他敏对胆碱能系统的双重作用。一项为期5个月的安慰剂对照研究的数据也表明,加兰他敏对行为症状有显著益处。加兰他敏产生的治疗效果的持续性和范围表明,它可能为AD患者提供额外的益处。

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