Biomarkers for Trials of Neuroprotection in Parkinson's Disease

被引:12
作者
Agarwal, Pankaj A. [1 ]
Stoessl, A. Jon [1 ,2 ]
机构
[1] Univ British Columbia, Pacific Parkinsons Res Ctr, Vancouver, BC V6T 2B5, Canada
[2] Vancouver Costal Hlth, Vancouver, BC, Canada
基金
加拿大健康研究院;
关键词
VESICULAR MONOAMINE TRANSPORTER; POSITRON-EMISSION-TOMOGRAPHY; METABOLIC NETWORK ACTIVITY; HUMAN CEREBROSPINAL-FLUID; SLEEP BEHAVIOR DISORDER; DOPAMINE TRANSPORTER; SUBSTANTIA-NIGRA; ALPHA-SYNUCLEIN; DIFFERENTIAL-DIAGNOSIS; OXIDATIVE STRESS;
D O I
10.1002/mds.25065
中图分类号
R74 [神经病学与精神病学];
学科分类号
100204 [神经病学];
摘要
With increased understanding of disease pathogenesis and the foreseeable reality of disease-modifying therapies, there is a growing need to find biomarkers that will allow early (preferably preclinical) detection of disease and that will provide an independent readout of disease progression. In this article, we review a variety of markers, with a focus on functional imaging techniques, which while imperfect, currently provide the best approach to this problem. We consider the limitations of functional imaging of the dopamine system in assessing the progression of Parkinson's Disease (PD) as well as the potential use of structural imaging and emerging progress in other biochemical and molecular markers. While there is no single biomarker that will satisfy all requirements, some combination is likely to be of great use in identifying those subjects most likely to benefit from neuroprotective therapies, as well as in monitoring the effects of these interventions. (C) 2012 Movement Disorder Society
引用
收藏
页码:71 / 85
页数:15
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