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单纤维肌电图中平均连续差值的离散度增加了重症肌无力的诊断敏感性。

Dispersion of mean consecutive differences in single-fiber electromyography increases diagnostic sensitivity for myasthenia gravis.

机构信息

Department of Neurology, Graduate School of Medicine, Chiba University, Chiba, Japan.

Department of Neurology, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.

出版信息

Muscle Nerve. 2021 Jun;63(6):885-889. doi: 10.1002/mus.27236. Epub 2021 Mar 31.

DOI:10.1002/mus.27236
PMID:33748989
Abstract

INTRODUCTION

In this study we aimed to investigate the dispersion of mean consecutive difference (MCD) of concentric needle jitter studies of patients with myasthenia gravis (MG) and its effect on diagnostic sensitivity for MG.

METHODS

One hundred fifty-three patients, including 76 patients with MG and 77 controls with possible MG who later received another diagnosis, underwent stimulated concentric needle jitter studies of the frontalis muscle. MCD mean, standard deviation (SD), and coefficient of variation (CV) were calculated. Diagnostic sensitivity and specificity were determined using receiver operating characteristic (ROC) analyses.

RESULTS

MG patients showed a significantly greater MCD mean (MG: control, 26.3 μs; 13.5 μs [median]; P < .0001), MCD SD (MG: control, 12.8 μs; 5.1 μs [median]; P < .0001), and MCD CV (MG: control, 46.1; 37.5 [median]; P < .001) than those without MG. An ROC curve of SD showed a large area under the curve (0.88), and a cut-off value of 7.2 μs, which was calculated by maximum Youden index, exhibited high diagnostic sensitivity (86%) for MG. Combined MCD mean, outliers, and SD criteria showed higher sensitivity (88%) than conventional criteria alone (82%), at the expense of lower specificity. Five MG patients with normal MCD mean and abnormal MCD SD had only ocular symptoms.

DISCUSSION

The dispersion of MCD as measured by MCD SD greater than 7.2 μs is significantly increased in patients with MG and may be a useful measure of abnormal jitter in the diagnosis of MG, especially for identifying patients with mild disease.

摘要

简介

本研究旨在探讨重症肌无力(MG)患者同心针颤搐研究的平均连续差异(MCD)的离散度及其对 MG 诊断敏感性的影响。

方法

153 例患者,包括 76 例 MG 患者和 77 例可能患有 MG 的对照患者,随后接受了额肌的刺激同心针颤搐研究。计算 MCD 均值、标准差(SD)和变异系数(CV)。使用接受者操作特征(ROC)分析确定诊断敏感性和特异性。

结果

MG 患者的 MCD 均值(MG:对照,26.3μs;13.5μs[中位数];P<0.0001)、MCD SD(MG:对照,12.8μs;5.1μs[中位数];P<0.0001)和 MCD CV(MG:对照,46.1;37.5[中位数];P<0.001)均显著大于无 MG 患者。SD 的 ROC 曲线显示曲线下面积较大(0.88),最大 Youden 指数计算得出的截断值为 7.2μs,对 MG 具有较高的诊断敏感性(86%)。结合 MCD 均值、异常值和 SD 标准的敏感性(88%)高于传统标准(82%),但特异性较低。5 例 MCD 均值正常但 MCD SD 异常的 MG 患者仅表现为眼肌症状。

讨论

MCD SD 测量的 MCD 离散度在 MG 患者中显著增加,可能是诊断 MG 异常颤搐的有用指标,特别是在识别轻度疾病患者方面。

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