Marker for a preclinical diagnosis of Parkinson's disease as a basis for neuroprotection.

Daniela Berg
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引用次数: 37

Abstract

Neuroprotective therapy is a pivotal aim in the treatment of the relentlessly progressive disorder Parkinson's disease. However, more than 60% of the dopaminergic neurons of the substantia nigra have already degenerated, when the diagnosis may be established. At this "advanced stage" neuroprotective strategies will - if at all - only have limited effect. It is, therefore, essential to establish markers to identify subjects at risk before motor manifestation. A number of such "premotor" signs have been discovered and investigated lately. Such signs include a genetic vulnerability and hyperechogenicity of the substantia nigra as well as premotor symptoms like olfactory and autonomic dysfunction, depression, REM sleep behaviour disorder, visual and neuropsychological impairment. Moreover, first signs of affection of the substantia nigra like PET and SPECT abnormalities and slight motor signs can be included, as they may be detected before a definite diagnosis can be made. Although most of these signs and symptoms are unspecific if singularly evaluated a combination of these features may indeed be valuable to detect a subgroup of the population at risk for PD. However, future studies are necessary to establish the predictive value of these "markers" singularly and in combination.

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作为神经保护基础的帕金森病临床前诊断的标志。
神经保护疗法是治疗帕金森病的关键目标。然而,超过60%的黑质多巴胺能神经元已经退化,当诊断可能成立。在这个“高级阶段”,神经保护策略将——如果有的话——只有有限的效果。因此,有必要在运动表现之前建立标志物来识别有危险的受试者。最近已经发现和研究了许多这样的“前运动”迹象。这些症状包括遗传易感性和黑质高回声性,以及运动前症状,如嗅觉和自主神经功能障碍、抑郁、快速眼动睡眠行为障碍、视觉和神经心理障碍。此外,黑质病变的最初迹象,如PET和SPECT异常和轻微的运动体征也可以包括在内,因为它们可以在做出明确诊断之前被检测到。虽然这些体征和症状大多是不特异性的,如果单独评估,这些特征的组合可能确实有价值,以检测有PD风险的人群亚组。然而,未来的研究需要确定这些“标记”的单独和组合的预测价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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