Grapperon A M, Attarian S
Centre de reference des maladies neuromusculaires et de la SLA, APHM, CHU Timone, 264 rue St Pierre, 13385 Marseille Cedex 05, France.
Centre de reference des maladies neuromusculaires et de la SLA, APHM, CHU Timone, 264 rue St Pierre, 13385 Marseille Cedex 05, France.
Rev Neurol (Paris). 2017 May;173(5):345-351. doi: 10.1016/j.neurol.2017.04.002. Epub 2017 Apr 28.
Neuronal and/or axonal hyperactivity and hyperexcitability is an important feature of motor neuron diseases. It results clinically in cramps and fasciculations. It is not specific to motor neuron diseases, and can occur in healthy subjects, as well as in various pathologies of the peripheral nervous system, including nerve hyperexcitability syndromes. Hyperexcitability plays an important and debated role in the pathophysiology of motor neuron diseases, especially in amyotrophic lateral sclerosis (ALS). The mechanisms causing hyperexcitability are not yet clearly identified. While most studies favor a distal axonal origin site of fasciculations, some of the fasciculations could be of cortical origin. The consequences of hyperexcitability are also discussed, whether it is rather protective or deleterious in the disease course. Fasciculations are depicted both clinically and using electromyogram, and more recently the interest of ultrasound has been highlighted. The importance of fasciculation potentials in the diagnosis of ALS led to changes in electrophysiological criteria at Awaji consensus conference. The contribution of these modifications to ALS diagnosis has been the subject of several studies. In clinical practice, it is necessary to distinguish fasciculations potentials of motor neuron disease from benign fasciculations. In most studies of fasciculation potentials in ALS, the presence of complex fasciculation potentials appears to be relevant for the diagnosis and the prognosis of the disease.
神经元和/或轴突的活动亢进及兴奋性过高是运动神经元疾病的一个重要特征。临床上会导致痉挛和肌束震颤。这并非运动神经元疾病所特有,在健康受试者以及包括神经兴奋性过高综合征在内的外周神经系统的各种病变中也可能出现。兴奋性过高在运动神经元疾病,尤其是肌萎缩侧索硬化症(ALS)的病理生理学中起着重要且存在争议的作用。导致兴奋性过高的机制尚未明确。虽然大多数研究倾向于肌束震颤起源于轴突远端,但部分肌束震颤可能起源于皮层。还讨论了兴奋性过高的后果,即在疾病进程中它究竟是具有保护作用还是有害作用。临床上以及通过肌电图对肌束震颤进行了描述,最近超声检查的作用也受到了关注。肌束震颤电位在ALS诊断中的重要性促使在淡路共识会议上对电生理标准进行了修订。这些修订对ALS诊断的贡献已成为多项研究的主题。在临床实践中,有必要区分运动神经元疾病的肌束震颤电位和良性肌束震颤。在大多数关于ALS中肌束震颤电位的研究中,复合肌束震颤电位的存在似乎与疾病的诊断和预后相关。