Phillips J G, Chiu E, Bradshaw J L, Iansek R
Psychology Department, Monash University, Clayton, Victoria, Australia.
Neuropsychologia. 1995 Mar;33(3):365-9. doi: 10.1016/0028-3932(94)00114-5.
This experiment asked whether Huntington's disease, like Parkinson's disease, another disorder of the basal ganglia, causes a specific progressive deficit in the performance of sequential movement. Ten patients with Huntington's disease and their age-matched controls wrote the lower-case letter "l" four times in a linked cursive script, upon a graphics tablet which sampled pen position at 200 Hz. Kinematic features of sequential movement (stroke length, stroke duration, peak velocity, time to peak velocity and time from peak to zero velocity) were examined in a Group by Stroke Position (2 x 8) design, to identify which aspects of movement might show progressive disturbances. Unlike Agostino et al. [Brain 115, 1481-1495, 1992], this experiment did in fact find progressive changes in the performance of sequential movements. Kinematic analysis indicated a progressive increase in movement duration during sequential movement, that was associated with the accelerative phase of movement.
本实验旨在探究亨廷顿病是否如帕金森病(另一种基底神经节疾病)一样,会导致连续运动表现出现特定的进行性缺陷。十名亨廷顿病患者及其年龄匹配的对照者,在一块以200赫兹采样笔位置的绘图板上,用连笔草书写小写字母“l”四次。采用组间×笔画位置(2×8)设计,对连续运动的运动学特征(笔画长度、笔画持续时间、峰值速度、达到峰值速度的时间以及从峰值到零速度的时间)进行检测,以确定运动的哪些方面可能表现出进行性紊乱。与阿戈斯蒂诺等人[《大脑》115卷,1481 - 1495页,1992年]不同的是,本实验确实发现连续运动表现存在进行性变化。运动学分析表明,连续运动过程中运动持续时间逐渐增加,这与运动的加速阶段有关。