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肌束颤动评分:肌萎缩侧索硬化症的敏感生物标志物。

Fasciculation score: a sensitive biomarker in amyotrophic lateral sclerosis.

机构信息

Department of Neurology, First Hospital, Shanxi Medical University, No.85, Jiefang South Street, Taiyuan, 030000, People's Republic of China.

出版信息

Neurol Sci. 2021 Nov;42(11):4657-4666. doi: 10.1007/s10072-021-05166-6. Epub 2021 Mar 11.

Abstract

OBJECTIVE

The aim of our study was to elucidate the characteristic of fasciculation distributions in amyotrophic lateral sclerosis (ALS) using a fasciculation score (FS) of muscle ultrasound (MUS) and to compare the diagnostic values of three MUS fasciculation parameters in patients.

METHODS

Thirty ALS patients, 16 ALS mimics, and 10 healthy subjects were involved. MUS of unilateral 10 muscles in each patient and needle electromyography (EMG) of total 204 muscles were performed to detect fasciculations and spontaneous activity respectively in ALS. Control groups underwent only MUS. Fasciculation was graded semiquantitatively with FS.

RESULTS

Three hundred fifty muscles in ALS and 260 in controls were examined. The fasciculation detection rates, total FS, the number of muscles with fasciculation, and the total number of fasciculations in ALS were all significantly higher than those of controls (P < 0.001). ALS patients exhibited a multifocal continuous pattern of fasciculation in limbs, whereas there were few fasciculations in controls. Compared with other parameters, total FS had the largest area under the curve (AUC) (AUC = 0.899, P < 0.001) in ALS diagnosis. The detection rates of lower motor neuron (LMN) acute lesions by MUS (70.6%) and EMG (72.1%) were nearly the same, and a positive correlation between the FS and spontaneous activity grades (P < 0.001, r = 0.359) was proved.

CONCLUSIONS

ALS patients exhibited the multifocal continuous pattern of fasciculation in limbs. FS showed high sensitivity and specificity in differentiating ALS from non-ALS patients, and the optimal cut-off value was determined as 4. The combination of MUS and EMG can provide additional information about specific muscles.

摘要

目的

本研究旨在通过肌超声(MUS)的肌束颤搐评分(FS)阐明肌萎缩侧索硬化症(ALS)中束颤搐分布的特征,并比较三种 MUS 束颤搐参数在患者中的诊断价值。

方法

纳入 30 例 ALS 患者、16 例 ALS 类似物患者和 10 例健康对照者。对每位患者的 10 块单侧肌肉进行 MUS 检查,并对总共 204 块肌肉进行针极肌电图(EMG)检查,以分别检测 ALS 中的束颤搐和自发性活动。对照组仅行 MUS 检查。采用 FS 对肌束颤搐进行半定量分级。

结果

共检查 ALS 患者 350 块肌肉和对照组 260 块肌肉。ALS 患者的肌束颤搐检出率、总 FS、出现肌束颤搐的肌肉数和肌束颤搐总数均显著高于对照组(P<0.001)。ALS 患者肢体呈现多灶性连续束颤搐模式,而对照组束颤搐较少。与其他参数相比,总 FS 在 ALS 诊断中具有最大的曲线下面积(AUC)(AUC=0.899,P<0.001)。MUS(70.6%)和 EMG(72.1%)检测下运动神经元(LMN)急性病变的检出率几乎相同,且 FS 与自发性活动分级呈正相关(P<0.001,r=0.359)。

结论

ALS 患者肢体呈现多灶性连续束颤搐模式。FS 对区分 ALS 与非 ALS 患者具有较高的敏感性和特异性,最佳截断值确定为 4。MUS 和 EMG 的联合使用可以提供关于特定肌肉的更多信息。

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