Institute for Cognitive Neuroscience, Biopsychology, Ruhr-University Bochum, Germany.
Sci Rep. 2013;3:1797. doi: 10.1038/srep01797.
In several neurodegenerative diseases, like Huntington's disease (HD), treatments are still lacking. To determine whether a treatment is effective, sensitive disease progression biomarkers are especially needed for the premanifest phase, since this allows the evaluation of neuroprotective treatments preventing, or delaying disease manifestation. On the basis of a longitudinal study we present a biomarker that was derived by integrating behavioural and neurophysiological data reflecting cognitive processes of action control. The measure identified is sensitive enough to track disease progression over a period of only 6 month. Changes tracked were predictive for a number of clinically relevant parameters and the sensitivity of the measure was higher than that of currently used parameters to track prodromal disease progression. The study provides a biomarker, which could change practice of progression diagnostics in a major basal ganglia disease and which may help to evaluate potential neuroprotective treatments in future clinical trials.
在一些神经退行性疾病中,如亨廷顿病(HD),仍然缺乏治疗方法。为了确定治疗是否有效,特别是在前显症期,需要敏感的疾病进展生物标志物,因为这可以评估预防或延迟疾病表现的神经保护治疗。基于一项纵向研究,我们提出了一种生物标志物,该标志物通过整合反映动作控制认知过程的行为和神经生理学数据得出。该测量方法足够敏感,可以在仅 6 个月的时间内跟踪疾病进展。跟踪到的变化可预测许多临床相关参数,并且该测量方法的灵敏度高于目前用于跟踪前病进展的参数。该研究提供了一种生物标志物,它可能会改变主要基底神经节疾病的进展诊断实践,并可能有助于在未来的临床试验中评估潜在的神经保护治疗。