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临床和电生理评估 alpha- dystroglycanopathy 队列(以 FKRP 为主)中的肌无力特征。

Clinical and electrophysiological evaluation of myasthenic features in an alpha-dystroglycanopathy cohort (FKRP-predominant).

机构信息

Department of Neurology, Massachusetts General Hospital, Boston, MA 02114, United States.

Department of Neurology, West Virginia University Hospitals, Morgantown, WV 26506, United States.

出版信息

Neuromuscul Disord. 2020 Mar;30(3):213-218. doi: 10.1016/j.nmd.2020.01.002. Epub 2020 Jan 25.

Abstract

A postsynaptic dysfunction of the neuromuscular junction has been reported in patients with alpha-dystroglycanopathy associated with mutations in guanosine diphosphate (GDP)-mannose pyrophosphorylase B gene (GMPPB), some of whom benefit from symptomatic treatment. In this study, we determine the frequency of myasthenic and fatigue symptoms and neuromuscular junction transmission defects in a fukutin-related protein (FKRP)-predominant alpha-dystroglycanopathy cohort. Thirty-one patients with alpha-dystroglycanopathies due to mutations in FKRP (n = 25), GMPPB (n = 4), POMGNT1 (n = 1), and POMT2 (n = 1) completed a six-question modified questionnaire for myasthenic symptoms and the PROMIS Short Form v1.0-Fatigue 8a survey, and they underwent 3 Hz repetitive nerve stimulation of spinal accessory nerve-trapezius and radial nerve-anconeus pairs. Results showed that fatigue with activity was common; 63% of the cohort reported fatigue with chewing. A defective postsynaptic neuromuscular junction transmission was not identified in any of the patients carrying FKRP mutations but only in one mildly affected patient with GMPPB mutations (c.79 G>C, p.D27H and c.402+1G>A, splice site variant). We conclude that symptoms of fatigue with activity did not predict abnormal neuromuscular junction transmission on electrodiagnostic studies in this cohort and that, unlike GMPPB subgroup, a defective neuromuscular junction transmission does not appear to be present in patients with FKRP-associated muscular dystrophies.

摘要

已报道在 GDP-甘露糖焦磷酸化酶 B 基因(GMPPB)突变相关的α-连接蛋白聚糖病患者中存在神经肌肉接头的突触后功能障碍,其中一些患者受益于对症治疗。在这项研究中,我们确定了 FKRP(n=25)、GMPPB(n=4)、POMGNT1(n=1)和 POMT2(n=1)突变所致的 FKRP 为主的α-连接蛋白聚糖病患者中肌无力和疲劳症状以及神经肌肉接头传递缺陷的发生率。31 名α-连接蛋白聚糖病患者(FKRP 突变 n=25、GMPPB 突变 n=4、POMGNT1 突变 n=1、POMT2 突变 n=1)完成了改良的 6 项肌无力症状问卷和 PROMIS 简短表单 v1.0-疲劳 8a 调查,并接受了面神经-胸锁乳突肌和桡神经-肱三头肌 3Hz 重复神经刺激。结果显示,活动时疲劳很常见;63%的患者报告咀嚼时疲劳。携带 FKRP 突变的患者中没有发现突触后神经肌肉接头传递缺陷,但仅在一名轻度受累的 GMPPB 突变患者中发现(c.79 G>C,p.D27H 和 c.402+1G>A,剪接位点变异)。我们的结论是,在该队列中,活动时疲劳症状并未预测电诊断研究中异常的神经肌肉接头传递,并且与 GMPPB 亚组不同,在 FKRP 相关肌营养不良症患者中似乎不存在神经肌肉接头传递缺陷。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7fa/7778731/de5b6ea916c1/nihms-1645197-f0001.jpg

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