Baslo M B, Coban A, Baykan B, Tutkavul K, Karli N, Saip S, Orhan E K, Ertas M
Department of Neurology, Istanbul University, Istanbul Faculty of Medicine, Istanbul, Turkey.
Cephalalgia. 2007 Nov;27(11):1201-5. doi: 10.1111/j.1468-2982.2007.01417.x. Epub 2007 Oct 5.
The aim of this study was to delineate any dysfunction of neuromuscular transmission (NMT) by single-fibre electromyography (SFEMG) in some rare types of migraine. Recent studies have shown subclinical dysfunction of NMT in migraine with aura and cluster headache by using SFEMG, whereas another recent study has shown NMT to be normal in familial hemiplegic migraine (FHM) with CACNA1A mutations. Thirty patients with rare primary headache syndromes [18 with sporadic hemiplegic migraine (SHM), six with FHM and six with basilar-type migraine (BM)] and 15 healthy control subjects without any headache complaints underwent nerve conduction studies, EMG and SFEMG during voluntary contraction of the extensor digitorum communis muscle. Ten to 20 different potential pairs were recorded and individual jitter values calculated. The results obtained from patient groups were compared with those from the normal subjects. Of 600 individual jitter values of the patients, 27 (4.5%) were abnormally high, whereas only 3/205 (1.5%) jitter values from normal subjects were abnormal. Abnormal NMT was found in 4/30 (13.3%) patients (three SHM and one BM), but in none of the control subjects. Only in SHM patients was the number of individual abnormal jitter values slightly but significantly different from normal controls. The present study demonstrates that subclinical NMT abnormality is slightly present in only SHM and BM patients, but not in FHM patients.
本研究的目的是通过单纤维肌电图(SFEMG)来描绘某些罕见类型偏头痛中神经肌肉传递(NMT)的任何功能障碍。最近的研究表明,使用SFEMG可发现有先兆偏头痛和丛集性头痛存在亚临床NMT功能障碍,而另一项最近的研究表明,携带CACNA1A突变的家族性偏瘫性偏头痛(FHM)患者的NMT是正常的。30例患有罕见原发性头痛综合征的患者[18例散发性偏瘫性偏头痛(SHM)、6例FHM和6例基底型偏头痛(BM)]以及15名无任何头痛主诉的健康对照者在指总伸肌随意收缩期间接受了神经传导研究、肌电图和SFEMG检查。记录了10至20对不同的电位,并计算了个体的颤抖值。将患者组获得的结果与正常受试者的结果进行比较。患者的600个个体颤抖值中,有27个(4.5%)异常升高,而正常受试者的205个颤抖值中只有3个(1.5%)异常。在30例患者中有4例(13.3%)发现NMT异常(3例SHM和1例BM),但对照组中无一例异常。仅在SHM患者中,个体异常颤抖值的数量与正常对照组相比略有但显著差异。本研究表明,仅SHM和BM患者中存在轻微的亚临床NMT异常,而FHM患者中不存在。