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不自主运动型帕金森病患者在未服药时表现出运动异常。

Dyskinetic Parkinson's disease patients demonstrate motor abnormalities off medication.

机构信息

Department of Neuroscience, Kinsmen Laboratory of Neurological Research, University of British Columbia, Rm. 2618, 2255 Wesbrook Mall, Vancouver V6T 1Z3, Canada.

出版信息

Exp Brain Res. 2011 Oct;214(3):471-9. doi: 10.1007/s00221-011-2845-2. Epub 2011 Aug 30.

Abstract

The pathophysiology of L-dopa-induced dyskinesias (LIDs) in Parkinson's disease (PD) remains poorly understood. The presence of superimposed LIDs clearly differentiates motor performance of dyskinetic from non-dyskinetic PD subjects when they are on medication, but here, we investigated whether their respective motor performance differs while subjects are off L-dopa medication and LIDs are not apparent. We assessed the motor performance of nine dyskinetic and ten non-dyskinetic PD subjects off L-dopa, and of ten age-matched control subjects, during a visually guided tracking task. As previous studies have suggested that linear dynamical system (LDS) models are useful to assess motor performance in PD in addition to overall tracking error, we used LDS models to assess the damping ratio parameter of motor behavior while controlling for disease severity. While overall tracking error did not significantly differ across groups, dyskinetic PD subjects demonstrated a significantly decreased mean damping ratio compared with control and non-dyskinetic PD subjects. For both groups, greater disease severity significantly predicted a lower damping ratio, but even after controlling for disease severity, the damping ratio for dyskinetic subjects was significantly lower. Our results demonstrate, somewhat counter-intuitively, that motor performance of dyskinetic and non-dyskinetic PD subjects differ, even off L-dopa when no dyskinesias are seen. A decreased damping ratio is indicative of a tendency to overshoot a target during motor performance, similar to the dysmetria found in cerebellar patients. We discuss the possibility of motor abnormalities in dyskinetic PD patients off medication in relation to altered functional cerebellar changes described in PD.

摘要

左旋多巴诱导的运动障碍(LIDs)在帕金森病(PD)中的病理生理学仍不清楚。当患者正在服用药物时,叠加的 LIDs 明显区分了运动障碍和非运动障碍 PD 患者的运动表现,但在这里,我们研究了在患者停止服用 L-多巴和 LIDs 不明显时,他们各自的运动表现是否不同。我们评估了九名运动障碍和十名非运动障碍 PD 患者在停止服用 L-多巴时以及十名年龄匹配的对照者在视觉引导跟踪任务中的运动表现。由于先前的研究表明线性动力系统(LDS)模型除了总体跟踪误差外,还可用于评估 PD 中的运动表现,因此我们使用 LDS 模型来评估运动行为的阻尼比参数,同时控制疾病严重程度。虽然总体跟踪误差在各组之间没有显著差异,但运动障碍 PD 患者的平均阻尼比明显低于对照组和非运动障碍 PD 患者。对于两组,疾病严重程度越大,阻尼比越低,但即使在控制了疾病严重程度后,运动障碍患者的阻尼比仍然明显更低。我们的结果表明,有些出人意料的是,即使在没有运动障碍的情况下,运动障碍和非运动障碍 PD 患者的运动表现也不同,甚至在停止服用 L-多巴时也是如此。阻尼比降低表明在运动表现中过度瞄准目标的趋势,类似于小脑患者中发现的运动失调。我们讨论了在停止服用药物的运动障碍 PD 患者中运动异常的可能性,与 PD 中描述的改变的功能性小脑变化有关。

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