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帕金森病的步态变化:非多巴胺能因素导致步态障碍的指标?

Gait variability in Parkinson's disease: an indicator of non-dopaminergic contributors to gait dysfunction?

机构信息

Clinical Ageing Research Unit, Campus for Ageing and Vitality, Institute for Ageing and Health, Newcastle University, Newcastle upon Tyne, NE4 5PL, UK.

出版信息

J Neurol. 2011 Apr;258(4):566-72. doi: 10.1007/s00415-010-5789-8. Epub 2010 Oct 30.

Abstract

Gait variability has potential utility as a predictive measure of dysfunction in Parkinson's disease (PD). Current understanding implicates non-dopaminergic pathways. This study investigated the explanatory characteristics of gait variability in PD on and off medication under single and dual task conditions. Fifty people with PD were assessed twice at home (on and off L: -dopa) whilst walking under single and dual task conditions, and variability (coefficient of variation, CV) was calculated for stride time and double limb support (DLS) time. Hierarchical regression analysis was used to identify predictors. The first block of variables included age, gait speed, depression (Hospital Anxiety and Depression Scale) and fatigue (Multidimensional Fatigue Inventory), and the second block included motor severity (UPDRS III), executive function (Hayling and Brixton) and attention (Test of Everyday Attention). Motor severity predicted stride time variability and DLS time variability independent of L: -dopa during single task gait. Dual task gait yielded a more complex picture. Depression made a unique contribution of 9.0% on medication and 5.0% off medication to stride time variability, and visual attention and younger age contributed to DLS variability on medication, explaining 3% and 2%, respectively. Motor severity predicted DLS variability off medication, explaining 74% of variance. Different characteristics explain the two measures of gait variability, pointing to different control mechanisms.

摘要

步态变异性有可能作为预测帕金森病(PD)功能障碍的一种手段。目前的研究认为与非多巴胺能通路有关。本研究探讨了 PD 患者在药物治疗和停药状态下单任务和双任务条件下步态变异性的解释特征。50 名 PD 患者在家中两次接受评估(服用和不服用 L:-多巴),在单任务和双任务条件下行走,计算步长时间和双下肢支撑(DLS)时间的变异性(变异系数,CV)。采用分层回归分析来确定预测因素。第一组变量包括年龄、步行速度、抑郁(医院焦虑和抑郁量表)和疲劳(多维疲劳量表),第二组变量包括运动严重程度(UPDRS III)、执行功能(Hayling 和 Brixton)和注意力(日常注意测试)。运动严重程度可独立于单任务行走时的 L:-多巴预测步长时间变异性和 DLS 时间变异性。双任务行走产生了更复杂的情况。抑郁对药物治疗时的步长时间变异性和停药时的步长时间变异性分别有 9.0%和 5.0%的独特贡献,视觉注意力和较年轻的年龄对药物治疗时的 DLS 变异性有贡献,分别解释了 3%和 2%。运动严重程度可预测停药时的 DLS 变异性,解释了 74%的变异性。两种步态变异性测量方法的不同特征解释了不同的控制机制。

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