[使用对症药物治疗痴呆]。

Takashi Kudo
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引用次数: 0

摘要

阿尔茨海默病(AD)的治疗大致可分为疾病修饰药物(DMD)和对症药物(SD)。DMD的主要策略是淀粉样蛋白疫苗治疗和β/γ-分泌酶抑制剂,它们已被寄予厚望作为AD的基础治疗方法。作为SD,多奈哌齐、加兰他明、利瓦斯汀和美金刚现在都可以使用。美金刚是一种NMDA受体抑制剂,其余三种药物是胆碱酯酶抑制剂。四种药物的抑制机制存在一定差异。虽然它们可能会提供正确使用的提示,但SD指南迄今为止表示SD之间没有显着差异。指南还指出,任何SD都不能阻止AD的进展,不应鼓励将其用于轻度认知损伤。有些人批评SD的使用,因为它们不是根治方法。相反,有一些报道称SD延缓AD的进展,保持ADL,减轻护理负担,并对BPSD有影响。因此,在与非药物治疗的适当结合下,SD的使用被认为是有价值的。
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[The Use of Symptomatic Drugs for Dementia].

The treatment of Alzheimer's disease (AD) can be roughly divided into Disease-modifying Drugs (DMD) and Symptomatic Drugs (SD). Major strategies of DMD are the amyloid vaccine therapy and β/γ-secretase inhibitors, which have been developed with high expectations as fundamental treatments for AD. As SD, donepezil, galantamine, rivastigmine, and memantine are now usable. While memantine is an NMDA receptor inhibitor, the remaining three agents are cholinesterase inhibitors. The inhibitory mechanisms of the four agents exhibit some differ- ences. Although they may offer tips for proper use, the SD guidelines have so far stated that there are no significant differences among SD. The guidelines also state that no SD can stop the progression of AD and that their use for MCI should not be encouraged. There are some criticisms about the use of SD because they are not root treatments. In contrast, there are some reports that SD delay AD progression, preserve ADL, reduce the care burden and have an effect on BPSD. Therefore, in proper combination with non-drug treat- ments, the use of SD is considered to be valuable.

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