Pacific Parkinson's Research Centre, University of British Columbia, Vancouver, British Columbia, Canada.
Mov Disord. 2013 Jan;28(1):71-85. doi: 10.1002/mds.25065. Epub 2012 Aug 24.
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.
随着对疾病发病机制的深入了解,以及可预见的疾病修饰疗法的出现,人们越来越需要找到生物标志物,以便能够早期(最好是临床前)检测到疾病,并提供疾病进展的独立指标。在本文中,我们综述了各种标记物,重点介绍了功能成像技术,尽管这些技术并不完美,但目前提供了最好的解决方法。我们考虑了功能成像多巴胺系统在评估帕金森病(PD)进展中的局限性,以及结构成像和其他生化和分子标记物的潜在用途。虽然没有一种单一的生物标志物能够满足所有要求,但某些组合可能非常有助于确定最有可能从神经保护治疗中获益的受试者,并监测这些干预措施的效果。