Department for Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy, University of Würzburg, Füchsleinstrasse 15, 97080 Würzburg, Germany.
J Neural Transm (Vienna). 2012 Jan;119(1):39-52. doi: 10.1007/s00702-011-0682-x. Epub 2011 Jul 14.
Reliable biomarkers that can be used for early diagnosis and tracking disease progression are the cornerstone of the development of disease-modifying treatments for Parkinson's disease (PD). The German Society of Experimental and Clinical Neurotherapeutics (GESENT) has convened a Working Group to review the current status of proposed biomarkers of neurodegeneration according to the following criteria and to develop a consensus statement on biomarker candidates for evaluation of disease-modifying therapeutics in PD. The criteria proposed are that the biomarker should be linked to fundamental features of PD neuropathology and mechanisms underlying neurodegeneration in PD, should be correlated to disease progression assessed by clinical rating scales, should monitor the actual disease status, should be pre-clinically validated, and confirmed by at least two independent studies conducted by qualified investigators with the results published in peer-reviewed journals. To date, available data have not yet revealed one reliable biomarker to detect early neurodegeneration in PD and to detect and monitor effects of drug candidates on the disease process, but some promising biomarker candidates, such as antibodies against neuromelanin, pathological forms of α-synuclein, DJ-1, and patterns of gene expression, metabolomic and protein profiling exist. Almost all of the biomarker candidates were not investigated in relation to effects of treatment, validated in experimental models of PD and confirmed in independent studies.
可靠的生物标志物可用于早期诊断和跟踪疾病进展,是开发帕金森病(PD)疾病修饰治疗的基石。德国实验和临床神经治疗学会(GESENT)召集了一个工作组,根据以下标准审查了拟议的神经退行性变生物标志物的现状,并就 PD 疾病修饰治疗评估的生物标志物候选物达成了共识声明。提出的标准是,该生物标志物应与 PD 神经病理学的基本特征和 PD 神经退行性变的机制相关,应与临床评分量表评估的疾病进展相关,应监测实际疾病状况,应在临床前得到验证,并至少由两名合格研究人员进行的两项独立研究确认,研究结果发表在同行评议的期刊上。迄今为止,尚无可靠的生物标志物可用于检测 PD 中的早期神经退行性变,也无法检测和监测候选药物对疾病进程的影响,但存在一些有前途的生物标志物候选物,如针对神经黑色素、α-突触核蛋白、DJ-1 和基因表达、代谢组学和蛋白质谱模式的病理性形式的抗体。几乎所有的生物标志物候选物都没有针对治疗效果进行研究,也没有在 PD 实验模型中进行验证,也没有在独立研究中得到证实。