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以佐米曲坦治疗帕金森病为重点的路易体痴呆的药物治疗管理。

Pharmacological management of dementia with Lewy bodies with a focus on zonisamide for treating parkinsonism.

机构信息

Unit of Epidemiological Research on Aging "Greatage Study", National Institute of Gastroenterology and Research Hospital IRCCS "S. De Bellis" Castellana Grotte , Bari, Italy.

Neurodegenerative Disease Unit, Department of Basic Medicine, Neuroscience, and Sense Organs, University of Bari Aldo Moro , Bari, Italy.

出版信息

Expert Opin Pharmacother. 2021 Feb;22(3):325-337. doi: 10.1080/14656566.2020.1828350. Epub 2020 Oct 6.

DOI:10.1080/14656566.2020.1828350
PMID:33021110
Abstract

INTRODUCTION

Dementia with Lewy bodies (DLB) has no approved symptomatic or disease-modifying treatments in the US and Europe, despite being the second most common cause of neurodegenerative dementia.

AREAS COVERED

Herein, the authors briefly review the DLB drug development pipeline, providing a summary of the current pharmacological intervention studies. They then focus on the anticonvulsant zonisamide, a benzisoxazole derivative with a sulfonamide group and look at its value for treating parkinsonism in DLB.

EXPERT OPINION

Several new compounds are being tested in DLB, the most innovative being those aimed at decreasing brain accumulation of α-synuclein. Unfortunately, new drug testing is challenging in terms of consistent diagnostic criteria and lack of reliable biomarkers. Few randomized controlled trials (RCTs) are well-designed, with enough power to detect significant drug effects. Levodopa monotherapy can treat the parkinsonism in DLB, but it can cause agitation or visual hallucination worsening. Two Phase II/III RCTs of DLB patients recently reported a statistically significant improvement in motor function in those receiving zonisamide as an adjunctive treatment to levodopa. New biomarker strategies and validated outcome measures for DLB or prodromal DLB may enhance clinical trial design for the development of specific disease-modifying treatments.

摘要

简介

尽管路易体痴呆(DLB)是仅次于阿尔茨海默病的第二大常见神经退行性痴呆病因,但在美国和欧洲,尚无针对其症状或疾病修饰的获批治疗方法。

涵盖领域

本文作者简要回顾了 DLB 的药物研发管道,总结了当前的药理学干预研究。然后,他们将重点介绍具有磺酰胺基团的苯并异恶唑衍生物抗癫痫药佐米曲坦,并探讨其在治疗 DLB 帕金森病中的价值。

专家意见

目前正在对几种新化合物进行 DLB 测试,其中最具创新性的是旨在减少大脑中α-突触核蛋白积累的化合物。不幸的是,新药物测试在诊断标准一致和缺乏可靠生物标志物方面具有挑战性。很少有设计良好的随机对照试验(RCT)具有足够的效力来检测出显著的药物作用。左旋多巴单药疗法可治疗 DLB 的帕金森病,但可能会引起激越或视觉幻觉恶化。最近两项针对 DLB 患者的 II/III 期 RCT 报告称,接受佐米曲坦作为左旋多巴辅助治疗的患者在运动功能方面有统计学意义的改善。新的生物标志物策略和针对 DLB 或前驱期 DLB 的经过验证的结局测量可能会增强特定疾病修饰治疗的临床试验设计。

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