Odabasi Z, Kuruoglu R, Oh S J
Department of Neurology, University of Alabama at Birmingham, The Veterans Affairs Medical Center, USA.
Acta Neurol Scand. 2000 May;101(5):315-20. doi: 10.1034/j.1600-0404.2000.90303.x.
The aims of this study were to investigate myopathic changes in myasthenia gravis (MG) by using turns-amplitude analysis (TAA) and quantitative motor unit potential duration analysis (MUPan), to correlate myopathic changes with severity and duration of the disease and the results of diagnostic tests including repetitive nerve stimulation test (RNS), single fiber electromyography (SFEMG), and anti-acetylcholine receptor antibody (AChR-ab), and to compare the sensitivities of these two methods in detecting myopathic changes in MG.
We studied both MUPan and TAA in 32 patients with MG.
The MUPan study showed myopathic changes in 12 patients (37.5%); TAA revealed a myopathic pattern in 4 (12.5%) and a neurogenic pattern in 4 cases (12.5%). Two of the 4 patients with a myopathic change by TAA also had short-duration mean MUP on the MUPan. No statistically significant association was found between the myopathic changes either by MUPan or TAA, and the various clinical and laboratory features.
We conclude that MUPan is a more sensitive method than TAA in showing myopathic changes in MG, and that TAA is of limited help in demonstrating them.
本研究旨在通过使用转折幅度分析(TAA)和定量运动单位电位时限分析(MUPan)来研究重症肌无力(MG)的肌病性改变,将肌病性改变与疾病的严重程度、病程以及包括重复神经电刺激试验(RNS)、单纤维肌电图(SFEMG)和抗乙酰胆碱受体抗体(AChR-ab)在内的诊断测试结果相关联,并比较这两种方法在检测MG肌病性改变中的敏感性。
我们对32例MG患者进行了MUPan和TAA研究。
MUPan研究显示12例患者(37.5%)存在肌病性改变;TAA显示4例(12.5%)有肌病模式,4例(12.5%)有神经源性模式。TAA显示有肌病性改变的4例患者中有2例在MUPan上的平均运动单位电位时限也较短。MUPan或TAA所显示的肌病性改变与各种临床和实验室特征之间未发现统计学上的显著关联。
我们得出结论,在显示MG的肌病性改变方面,MUPan比TAA更敏感,而TAA在证明这些改变方面帮助有限。