Clinical and Translational Science Institute.
Departments of Neurology, Neuroscience, and Pediatrics, University of Rochester, Rochester, NY.
Ann Neurol. 2018 Jan;83(1):52-60. doi: 10.1002/ana.25121. Epub 2018 Jan 10.
Dystonia is a movement disorder that has been associated with impaired motor learning and sequence recognition. However, despite evidence that patients with dystonia have a reduced sense of agency, it is unclear whether dystonia is specifically associated with impaired recognition of a movement sequence. We have shown previously that performance consistency in the temporal and kinematic domains predicts awareness of underlying motor patterns in a finger-tapping task. Since movements in dystonia are characterized by high variability, we predicted that subjects with dystonia would have decreased motor sequence awareness.
Subjects with dystonia (n = 20) and healthy control adults (n = 30) performed finger-tapping sequences with a common motor pattern and changing stimulus-to-response mappings. Subjects were said to be "aware" of the motor pattern if they recognized that their fingers moved in the same order during each stimulus-to-response remapping.
Subjects with dystonia had decreased motor pattern awareness, but those differences were not due to greater performance variability. Subjects with dystonia tapped sequences as series of discrete movements, rather than as a combined series.
Dystonia is associated with impaired recognition of a repeating movement pattern. This difference may result from a strategy of separating sequential elements and attending to them individually. Ann Neurol 2018;83:52-60.
肌张力障碍是一种运动障碍,与运动学习和序列识别受损有关。然而,尽管有证据表明肌张力障碍患者的主体感降低,但尚不清楚肌张力障碍是否与对运动序列的识别受损具体相关。我们之前已经表明,在时间和运动学领域的表现一致性可以预测在手指敲击任务中对潜在运动模式的意识。由于肌张力障碍患者的运动具有高度可变性,我们预测肌张力障碍患者的运动序列意识会降低。
患有肌张力障碍的受试者(n=20)和健康对照组成年人(n=30)以共同的运动模式执行手指敲击序列,并改变刺激-反应映射。如果受试者在每个刺激-反应重新映射时都意识到他们的手指以相同的顺序移动,则认为他们“意识到”运动模式。
患有肌张力障碍的受试者的运动模式意识降低,但这些差异不是由于更大的性能变异性引起的。患有肌张力障碍的受试者将序列敲击为离散的运动序列,而不是组合序列。
肌张力障碍与对重复运动模式的识别受损有关。这种差异可能是由于分离序列元素并单独关注它们的策略所致。神经病学年鉴 2018;83:52-60。