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帕金森病中未满足的医疗需求。

Unmet medical needs in Parkinson's disease.

作者信息

Koller William C, Tse Winona

机构信息

Department of Neurology, Mt. Sinai School of Medicine, New York, NY 10029, USA.

出版信息

Neurology. 2004 Jan 13;62(1 Suppl 1):S1-8. doi: 10.1212/wnl.62.1_suppl_1.s1.

DOI:10.1212/wnl.62.1_suppl_1.s1
PMID:14718675
Abstract

Levodopa, introduced in the late 1960s, was the first highly effective drug for the symptomatic treatment of Parkinson's disease (PD) and remains the mainstay of pharmacologic treatment. However, long-term treatment has important limitations. The disease continues to progress despite treatment with levodopa, and a neuroprotective therapy is urgently required. In addition, motor complications associated with chronic levodopa therapy are an important source of disability. Treatment of these complications forms a major focus of modern PD management, and it is in this area that recent advances in our knowledge offer the best opportunity for therapeutic gain. In the search for improved therapies, suitable outcome measures to better assess overall disability in PD and disease progression are essential.

摘要

左旋多巴于20世纪60年代末问世,是首个用于帕金森病(PD)症状性治疗的高效药物,至今仍是药物治疗的主要手段。然而,长期治疗存在重要局限性。尽管使用左旋多巴进行治疗,疾病仍在进展,因此迫切需要一种神经保护疗法。此外,与慢性左旋多巴治疗相关的运动并发症是致残的重要原因。这些并发症的治疗是现代帕金森病管理的主要重点,正是在这一领域,我们知识的最新进展为治疗获益提供了最佳机会。在寻求改进疗法的过程中,合适的结局指标对于更好地评估帕金森病的整体残疾程度和疾病进展至关重要。

相似文献

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Unmet medical needs in Parkinson's disease.帕金森病中未满足的医疗需求。
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Neuroprotective therapy in Parkinson's disease and motor complications: a search for a pathogenesis-targeted, disease-modifying strategy.帕金森病与运动并发症的神经保护治疗:探寻针对发病机制的疾病修饰策略。
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Levodopa in the early treatment of Parkinson's disease.左旋多巴在帕金森病早期治疗中的应用
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Medical management of levodopa-associated motor complications in patients with Parkinson's disease.帕金森病患者左旋多巴相关运动并发症的药物治疗
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引用本文的文献

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Functional Characterization of Novel Circular RNA Molecule, circzip-2 and Its Synthesizing Gene zip-2 in C. elegans Model of Parkinson's Disease.新型环状 RNA 分子 circzip-2 及其在帕金森病线虫模型中合成基因 zip-2 的功能特征。
Mol Neurobiol. 2018 Aug;55(8):6914-6926. doi: 10.1007/s12035-018-0903-5. Epub 2018 Jan 23.
2
Greater improvement in LRRK2 G2019S patients undergoing Subthalamic Nucleus Deep Brain Stimulation compared to non-mutation carriers.与非突变携带者相比,接受丘脑底核深部脑刺激的LRRK2 G2019S患者有更大改善。
BMC Neurosci. 2016 Feb 1;17:6. doi: 10.1186/s12868-016-0240-4.
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Timing of deep brain stimulation in Parkinson disease: a need for reappraisal?
帕金森病中深部脑刺激的时机:是否需要重新评估?
Ann Neurol. 2013 May;73(5):565-75. doi: 10.1002/ana.23890.
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Clinical aspects and management of levodopa-induced dyskinesia.左旋多巴诱导运动障碍的临床方面和管理。
Parkinsons Dis. 2012;2012:745947. doi: 10.1155/2012/745947. Epub 2012 Jun 3.
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Short non-coding RNA biology and neurodegenerative disorders: novel disease targets and therapeutics.短链非编码RNA生物学与神经退行性疾病:新的疾病靶点与治疗方法
Hum Mol Genet. 2009 Apr 15;18(R1):R27-39. doi: 10.1093/hmg/ddp070.
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Optimising levodopa therapy for the management of Parkinson's disease.优化左旋多巴疗法以治疗帕金森病
J Neurol. 2005 Oct;252 Suppl 4:IV43-IV48. doi: 10.1007/s00415-005-4009-4.