Raccagni Cecilia, Löscher Wolfgang N, Stefani Ambra, Wanschitz Julia, Kraemer Lena, Heidbreder Anna, Högl Birgit
Department of Neurology, Innsbruck Medical University, Innsbruck, Austria.
Department of Neurology, Innsbruck Medical University, Innsbruck, Austria.
Sleep Med. 2016 Jun;22:61-64. doi: 10.1016/j.sleep.2016.04.018. Epub 2016 Jun 7.
Excessive fragmentary myoclonus is a frequent incidental finding in patients undergoing polysomnography for other reasons. The aim of this study was to evaluate whether electrophysiological examination in patients with excessive fragmentary myoclonus during sleep according to American Academy of Sleep Medicine (AASM) criteria shows findings of peripheral nerve dysfunction.
Ninety-eight of 100 patients with excessive fragmentary myoclonus detected as an incidental finding during routine polysomnography underwent electrophysiological workup. Motor nerve conduction studies of the right peroneal and tibial nerves, F-wave recordings of the tibial nerve, antidromic sensory nerve conduction studies of the left sural nerve and needle electromyography of the right tibialis anterior muscle were performed and classified as normal, peripheral neuropathy, lumbar 5 (L5) nerve root lesion, or benign fasciculations.
Fifty percent (49 out of 98) presented with electrophysiological abnormalities, most frequently polyneuropathy (32 out of 49, 65.3%), followed by L5 nerve root lesions (13 out of 49, 26.5%) and benign fasciculations (4 out of 49, 8.2%). Patients with electrophysiological abnormalities were older than those without.
The high prevalence of abnormal neurophysiological findings in patients with excessive fragmentary myoclonus during polysomnography suggests that excessive fragmentary myoclonus during sleep according to AASM criteria is not primarily a sleep-related phenomenon, but only persists during sleep and points to peripheral nerve pathology at least in part of the cases. Patients with incidental EFM during polysomnography should undergo electrophysiological workup for peripheral nerve pathology.
过度片段性肌阵挛在因其他原因接受多导睡眠图检查的患者中是常见的偶然发现。本研究的目的是评估根据美国睡眠医学学会(AASM)标准,睡眠中出现过度片段性肌阵挛的患者进行电生理检查是否显示周围神经功能障碍的结果。
在常规多导睡眠图检查中偶然发现的100例过度片段性肌阵挛患者中,98例接受了电生理检查。对右侧腓总神经和胫神经进行运动神经传导研究,对胫神经进行F波记录,对左侧腓肠神经进行逆向感觉神经传导研究,并对右侧胫前肌进行针极肌电图检查,并将结果分类为正常、周围神经病变、腰5(L5)神经根病变或良性肌束震颤。
50%(98例中的49例)存在电生理异常,最常见的是多发性神经病(49例中的32例,65.3%),其次是L5神经根病变(49例中的13例,26.5%)和良性肌束震颤(49例中的4例,8.2%)。有 电生理异常的患者比无异常的患者年龄更大。
多导睡眠图检查中过度片段性肌阵挛患者神经生理异常结果的高发生率表明,根据AASM标准,睡眠中的过度片段性肌阵挛并非主要是与睡眠相关的现象,而只是在睡眠期间持续存在,并且至少在部分病例中提示周围神经病变。在多导睡眠图检查中偶然发现EFM的患者应接受周围神经病变的电生理检查。