Krampfl Klaus, Mohammadi Bahram, Komissarow Leonid, Dengler Reinhard, Bufler Johannes
Department of Neurology, Medical University of Hannover, Hannover, Germany.
Amyotroph Lateral Scler Other Motor Neuron Disord. 2004 Sep;5(3):154-63. doi: 10.1080/14660820410019657.
It can be difficult to detect upper motor neuron (UMN) involvement in early amyotrophic lateral sclerosis (ALS). The present study tested the usefulness of mirror movements (MMs), i.e., contralateral coactivation of hand muscles, as a UMN sign in ALS. Thirty-seven patients with possible, probable or definite ALS and 19 patients with suspected ALS without clinical signs of UMN involvement, 21 disease controls and 15 healthy volunteers were included. MMs were studied clinically, electromyographically and by transcranial magnetic stimulation (TMS), looking for ipsilateral motor evoked potentials (IMEPs). MMs were observed clinically in 15 ALS patients (27%) and electromyographically in 28 (50%). IMEPs in the abductor pollicis brevis muscle following TMS were recorded in 34 (61%) of all ALS patients and in nine (47%) out of 19 patients with suspected ALS, but not in healthy controls. Central motor conduction times were prolonged in 15 ALS patients (27%). It is concluded that MMs, especially if studied by EMG and TMS (IMEPs) can essentially improve detection of UMN involvement, especially in early stages of ALS.
在早期肌萎缩侧索硬化症(ALS)中,检测上运动神经元(UMN)受累情况可能具有挑战性。本研究测试了镜像运动(MMs),即手部肌肉的对侧共同激活,作为ALS中UMN体征的效用。研究纳入了37例可能、很可能或确诊的ALS患者、19例疑似ALS但无UMN受累临床体征的患者、21例疾病对照者和15名健康志愿者。通过临床、肌电图和经颅磁刺激(TMS)研究MMs,寻找同侧运动诱发电位(IMEPs)。15例ALS患者(27%)临床观察到MMs,28例(50%)肌电图观察到MMs。在所有ALS患者中的34例(61%)以及19例疑似ALS患者中的9例(47%)记录到TMS后拇短展肌的IMEPs,但健康对照者未记录到。15例ALS患者(27%)的中枢运动传导时间延长。得出的结论是,MMs,尤其是通过肌电图和TMS(IMEPs)进行研究时,可显著改善UMN受累情况的检测,尤其是在ALS的早期阶段。