Muratori Lisa M, Reilmann Ralf, Gordon Andrew M
Department of Biobehavioral Science, Teachers College, Columbia University, 525 West 120th Street, New York, NY 10027, USA.
Neuropsychologia. 2003;41(11):1498-508. doi: 10.1016/s0028-3932(03)00092-7.
While the pathology and autonomic nervous system components of multiple system atrophy (MSA) have been well described, little is known about the associated motor dysfunction. One prominent feature of MSA is parkinsonism, although ataxias and pyramidal tract signs are frequently present. To investigate the nature of motor deficits in MSA, a natural grip-lift movement requiring a precision grasp was used to examine force coordination. Subjects were asked to grasp an instrumented object using the fingertips of the thumb and index finger and lift it 10 cm above the table surface. Subjects with MSA demonstrated a prolonged duration between object contact and initiation of the lifting drive that increased with the weight of the object. During this period these subjects produced large grasping forces generating a significant portion of the eventual grip force employed to hold the object. In contrast, control subjects generated grip and load forces in parallel after establishing contact with the object. Therefore, subjects with MSA showed a disrupted performance on both the sequential (grasp, then lift) and simultaneous (grip and load force development) portions of this task. Only after initiation of the vertical lifting drive did subjects with MSA generate forces in a similar manner to control subjects. These findings demonstrate that subjects with MSA exhibit a disrupted coordination of grasp and could suggest a general deficit in motor control resulting from multi-focal neural degeneration.
虽然多系统萎缩(MSA)的病理学和自主神经系统成分已得到充分描述,但对其相关的运动功能障碍却知之甚少。MSA的一个突出特征是帕金森综合征,尽管共济失调和锥体束征也经常出现。为了研究MSA中运动缺陷的本质,我们使用了一种需要精确抓握的自然抓握-提起动作来检查力量协调。要求受试者用拇指和食指的指尖抓住一个装有传感器的物体,并将其举到桌面上方10厘米处。MSA患者在物体接触与提起动作启动之间的持续时间延长,且随着物体重量的增加而增加。在此期间,这些患者会产生较大的抓握力,这些抓握力在最终用于握住物体的握力中占很大一部分。相比之下,对照组受试者在与物体接触后会同时产生握力和负载力。因此,MSA患者在这项任务的顺序部分(先抓握,然后提起)和同时部分(握力和负载力的发展)的表现都受到了干扰。只有在开始垂直提起动作后,MSA患者才会以与对照组受试者相似的方式产生力量。这些发现表明,MSA患者表现出抓握协调受损,这可能暗示多灶性神经变性导致的运动控制普遍缺陷。