[Pharmacological Interventions in Dementia].

Q4 Medicine
Miho Ota, Tetsuaki Arai
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引用次数: 0

Abstract

Pharmacological interventions for dementia include medications aimed at alleviating its core symptom: cognitive dysfunction. These medicines are known as anti-dementia drugs. As our understanding of Alzheimer's disease (AD) has advanced, the amyloid hypothesis stating that amyloid proteins are involved in the pathogenesis of AD has been proposed. To date, anti-dementia drugs such as cholinesterase inhibitors and N-methyl-D-aspartate receptor antagonists have focused on symptomatic treatment. In recent years, based on the amyloid hypothesis, the development of medicines that target either (1) the enzyme that produces amyloid beta (Aβ) or (2) Aβ itself, has been promoted as a treatment strategy for AD. In 2021, the first drug targeting Aβ, aducanumab, was launched in the USA. In Japan, lecanemab and donanemab are now available as monoclonal antibodies targeting Aβ. Additionally, medications have been used to manage the behavioral and psychological symptoms of dementia (BPSD), Parkinsonism, and rapid eye movement sleep behavior disorder. Furthermore, dementia is a major risk factor for delirium, which often occurs during the course of dementia. In this study, we introduce pharmacotherapy with anti-dementia drugs, BPSD treatment, and delirium.

[痴呆症的药物干预]。
痴呆症的药理学干预包括旨在减轻其核心症状:认知功能障碍的药物。这些药物被称为抗痴呆症药物。随着我们对阿尔茨海默病(AD)认识的不断深入,淀粉样蛋白假说(amyloid hypothesis)提出了淀粉样蛋白参与AD的发病机制。迄今为止,抗痴呆药物如胆碱酯酶抑制剂和n -甲基-d -天冬氨酸受体拮抗剂主要集中在对症治疗上。近年来,基于淀粉样蛋白假说,开发针对(1)产生β淀粉样蛋白(a β)的酶或(2)β淀粉样蛋白本身的药物,已被作为一种治疗AD的策略。2021年,首个靶向Aβ的药物aducanumab在美国上市。在日本,lecanemab和donanemab现在作为靶向Aβ的单克隆抗体可用。此外,药物已被用于控制痴呆(BPSD)、帕金森病和快速眼动睡眠行为障碍的行为和心理症状。此外,痴呆症是谵妄的主要危险因素,谵妄经常发生在痴呆症的过程中。在这项研究中,我们介绍了抗痴呆药物,BPSD治疗和谵妄的药物治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Neurological Surgery
Neurological Surgery Medicine-Medicine (all)
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