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Insights into cognitive decline in spinocerebellar Ataxia type 2: a P300 event-related brain potential study

机译:对2型脊髓小脑共济失调认知能力下降的见解:一项与P300事件相关的脑潜能研究

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Background Cognitive decline is a common non-motor feature characterizing Spinocerebellar Ataxia type 2 (SCA2) during the prodromal stage, nevertheless a reduced number of surrogate biomarkers of these alterations have been described. Objective To provide insights into cognitive dysfunction in SCA2 patients using P300 event-related potentials (ERP) and to evaluate these measures as biomarkers of the disease. Methods A cross-sectional study was performed with 30 SCA2 patients, 20 preclinical carriers and 33 healthy controls, who underwent visual, auditory P300 ERPs, and neurological examinations and ataxia scoring. Results SCA2 patients showed significant increase in P300 latencies and decrease of P300 amplitudes for visual and auditory stimuli, whereas preclinical carriers exhibit a less severe, but significant prolongation of P300 latencies. Multiple regression analyses disclosed a significant effect of SARA score on visual P300 abnormalities in patients as well as of the time to ataxia onset on visual P300 latencies in preclinical carriers. Conclusions This paper demonstrated the role of P300 ERP for the study of attentional, discriminative and working memory abnormalities in SCA2 patients and for the search of surrogate biomarkers from prodromal to the symptomatic stages. Moreover, our findings provide psychophysiological evidences supporting the cerebellar involvement in cognitive processes and allows us to identify promising outcome measures for future trials focusing on cognitive dysfunction.
机译:背景认知功能减退是前驱期特征性2型脊髓小脑共济失调(SCA2)的常见非运动功能,但已描述了这些改变的替代生物标志物数量减少。目的利用P300事件相关电位(ERP)了解SCA2患者的认知功能障碍,并评估这些措施作为疾病的生物标志物。方法对30例SCA2患者,20例临床前携带者和33例健康对照者进行了横断面研究,他们接受了视觉,听觉P300 ERPs以及神经系统检查和共济失调评分。结果SCA2患者显示视觉和听觉刺激的P300潜伏期显着增加,而P300振幅降低,而临床前携带者表现出的P300潜伏期较轻,但显着延长。多元回归分析显示,SARA评分对患者的视觉P300异常有显着影响,并且对临床前携带者的视觉P300潜伏期发生共济失调的时间也有显着影响。结论本文证明了P300 ERP在研究SCA2患者的注意,区分和工作记忆异常以及从前驱阶段到有症状阶段寻找替代生物标志物方面的作用。此外,我们的发现提供了支持小脑参与认知过程的心理生理证据,并使我们能够为有前景的针对认知功能障碍的试验确定有希望的结果指标。

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