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帕金森病运动和认知功能障碍的共同原则。

Joint principles of motor and cognitive dysfunction in Parkinson's disease.

机构信息

Max Planck Institute for Neurological Research, Gleueler Str. 50, D-50931 Cologne, Germany.

出版信息

Neuropsychologia. 2013 Jul;51(8):1417-25. doi: 10.1016/j.neuropsychologia.2013.04.011. Epub 2013 Apr 27.

Abstract

Traditionally, the lateral premotor cortex (PM) is assigned a role in stimulus-driven rather than memory-driven motor control, whereas the opposite holds for the mesial premotor cortex (supplementary motor area, SMA). Consistently, patients with Parkinson's Disease (PD), in which a specific functional degradation of the mesial loop (i.e., SMA-Striatum) occurs, show impaired memory-driven but relatively preserved stimulus-driven motor control. However, both parts of the premotor cortex are involved in perceptual prediction tasks as well. Here we tested whether the functional bias described on the motor level (i.e., memory-driven/mesial versus stimulus-driven/lateral) can also be detected in perceptual prediction tasks thereby suggesting that PD patients exhibit the same pattern of impaired memory-driven and preserved stimulus-driven control in the cognitive domain. To this end, we investigated 20 male PD-patients "on" and "off" dopaminergic medication while performing a serial prediction task (SPT). A specific modification was implemented to the classical SPT (SPT0) that caused shifts from stimulus- to memory-based prediction (SPT+). As a result, PD patients showed a significantly impaired performance "off" compared to "on" medication for SPT+, whereas no significant "on"/"off"-effects were found for SPT0. Descriptively, the "off"-performance decreased gradually with increasing demands on memory-based prediction. Furthermore, the severity of motor deficits according to the UPDRS III correlated significantly with impaired performance in SPT0 "on" medication. Importantly, an even stronger dependency was found for UPDRS III and SPT+. These findings point to a role of the SMA-striatal loop in memory-driven serial prediction beyond the motor domain.

摘要

传统上,外侧前额皮质(PM)被认为在刺激驱动而非记忆驱动的运动控制中起作用,而内侧前额皮质(补充运动区,SMA)则相反。一致地,患有帕金森病(PD)的患者,其中内侧环路(即 SMA-纹状体)发生特定的功能退化,表现出记忆驱动的运动控制受损但相对保留的刺激驱动运动控制。然而,前额皮质的两部分都参与了知觉预测任务。在这里,我们测试了在运动水平上描述的功能偏向(即记忆驱动/内侧与刺激驱动/外侧)是否也可以在知觉预测任务中检测到,从而表明 PD 患者在认知领域表现出相同的记忆驱动受损和刺激驱动保留的控制模式。为此,我们在执行序列预测任务(SPT)时,研究了 20 名男性 PD 患者“开”和“关”多巴胺药物。对经典 SPT(SPT0)进行了特定的修改,导致从刺激到基于记忆的预测(SPT+)的转变。结果,与“开”药物相比,PD 患者在“关”药物时的 SPT+表现明显受损,而对于 SPT0 则没有发现显著的“开”/“关”效应。描述性地,“关”表现随着基于记忆的预测需求的增加而逐渐下降。此外,根据 UPDRS III 评估的运动缺陷严重程度与 SPT0 药物治疗时的表现受损显著相关。重要的是,在 UPDRS III 和 SPT+之间发现了更强的依赖性。这些发现表明 SMA-纹状体环路在记忆驱动的序列预测中起作用,超越了运动领域。

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