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胆碱酯酶抑制剂能延缓阿尔茨海默病的进展吗?

Do cholinesterase inhibitors slow progression of Alzheimer's disease?

作者信息

Farlow M R

机构信息

Indiana University School of Medicine, Indianapolis, USA.

出版信息

Int J Clin Pract Suppl. 2002 Jun(127):37-44.

Abstract

In the absence of a cure for Alzheimer's disease (AD), treatment has focused on therapy to provide symptomatic benefits and to slow progression of the disease, so that patients can maintain their independence for as long as possible. New research suggests that rivastigmine, a potent, pseudo-irreversible inhibitor of both acetylcholinesterase (AChE) and butyrylcholinesterase that shows preferential selectivity for the G1 form of AChE, may provide symptomatic and disease progression slowing effects. The drug's pharmacological properties may help to slow the conversion of diffuse, benign amyloid plaques to neuritic plaques associated with clinical dementia. In 'delayed-start' paradigms--open-label extensions of placebo-controlled studies involving mild to moderate AD patients--the treatment effects of rivastigmine on cognitive and non-cognitive outcomes at 52 weeks were even greater than those observed at 26 weeks, and patients who received rivastigmine for the entire 52 weeks had better outcomes than those who received rivastigmine only for the latter 26 weeks (having received placebo for the first 26 weeks during the placebo-controlled phase). These treatment effects were even more robust in patients with moderately severe disease, indicating that the sustained long-term benefits of rivastigmine apply across the continuum of disease severity. The results seen in those patients with mild and moderately severe AD suggest that the progression of AD was being slowed in treated patients and that a disease-modifying effect may have been taking place. The effects of rivastigmine on cognition remain clinically relevant for at least 2 years, with benefits over projected placebo increasing over time. The long-term benefits of rivastigmine have also been reported in behavioural domains of patients with mild to moderate AD for 104 weeks and in patients with the Lewy body variant of AD for 96 weeks. Rivastigmine may slow AD progression, allowing patients to maintain autonomy for longer.

摘要

在尚无治愈阿尔茨海默病(AD)方法的情况下,治疗重点在于提供对症治疗并减缓疾病进展,以使患者尽可能长时间保持独立。新研究表明,卡巴拉汀是一种强效、伪不可逆的乙酰胆碱酯酶(AChE)和丁酰胆碱酯酶抑制剂,对AChE的G1形式具有优先选择性,可能具有对症治疗和减缓疾病进展的作用。该药物的药理特性可能有助于减缓弥漫性良性淀粉样斑块向与临床痴呆相关的神经炎性斑块的转化。在“延迟启动”模式中——涉及轻度至中度AD患者的安慰剂对照研究的开放标签扩展——卡巴拉汀在52周时对认知和非认知结果的治疗效果甚至比26周时观察到的效果更大,接受卡巴拉汀治疗满52周的患者比仅在后26周接受卡巴拉汀治疗(在安慰剂对照阶段的前26周接受安慰剂)的患者预后更好。这些治疗效果在中度严重疾病患者中更为显著,表明卡巴拉汀的长期持续益处适用于整个疾病严重程度范围。在轻度和中度严重AD患者中观察到的结果表明,接受治疗的患者中AD的进展正在减缓,并且可能已经发生了疾病修饰作用。卡巴拉汀对认知的影响在临床上至少持续2年,与预计安慰剂相比的益处随时间增加。卡巴拉汀的长期益处也在轻度至中度AD患者的行为领域中报道了104周,在路易体变异型AD患者中报道了96周。卡巴拉汀可能减缓AD进展,使患者能够更长时间保持自主能力。

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