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改变帕金森病诊断的研究标准:障碍与机遇。

Changing the research criteria for the diagnosis of Parkinson's disease: obstacles and opportunities.

机构信息

Department of Neurodegeneration, Hertie-Institute of Clinical Brain Research, University of Tübingen, 72070 Tübingen, Germany.

出版信息

Lancet Neurol. 2013 May;12(5):514-24. doi: 10.1016/S1474-4422(13)70047-4. Epub 2013 Apr 11.

Abstract

Recent findings question our present understanding of Parkinson's disease and suggest that new research criteria for the diagnosis of Parkinson's disease are needed, similar to those recently defined in Alzheimer's disease. However, our ability to redefine Parkinson's disease is hampered by its complexity and heterogeneity in genetics, phenotypes, and underlying molecular mechanisms; the absence of biochemical markers or ability to image Parkinson's disease-specific histopathological changes; the long prodromal period during which non-motor manifestations might precede classic motor manifestations; and uncertainty about the status of disorders diagnosed clinically as Parkinson's disease but without Lewy pathology. Although it is too early to confidently redefine Parkinson's disease, the time has come to establish a research framework that could lead to new diagnostic criteria. We propose the establishment of three tiers encompassing clinical features, pathological findings, and genetics or molecular mechanisms. Specific advances in each tier, bridged by neuroimaging and biochemical data, will eventually lead to a redefinition of Parkinson's disease.

摘要

最近的发现质疑了我们目前对帕金森病的理解,并表明需要为帕金森病的诊断制定新的研究标准,类似于最近在阿尔茨海默病中定义的标准。然而,由于帕金森病在遗传学、表型和潜在分子机制方面的复杂性和异质性、缺乏生物化学标志物或能够对帕金森病特异性组织病理学变化进行成像的能力、在非运动表现可能先于经典运动表现之前的较长前驱期以及对临床上诊断为帕金森病但无路易体病理的疾病状态的不确定性,我们重新定义帕金森病的能力受到了阻碍。虽然现在重新定义帕金森病还为时过早,但建立一个可能导致新的诊断标准的研究框架的时机已经成熟。我们建议建立一个包含临床特征、病理学发现以及遗传学或分子机制的三个层次的框架。通过神经影像学和生化数据连接的每个层次的具体进展,最终将导致对帕金森病的重新定义。

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