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2
[Amyotrophic lateral sclerosis and respiratory insufficiency].[肌萎缩侧索硬化症与呼吸功能不全]
Duodecim. 2015;131(2):127-35.
3
[Standardization of spirometry: 2015 update. Published by German Atemwegsliga, German Respiratory Society and German Society of Occupational and Environmental Medicine].[肺量计标准化:2015年更新版。由德国呼吸联盟、德国呼吸学会以及德国职业与环境医学学会发布]
Pneumologie. 2015 Mar;69(3):147-64. doi: 10.1055/s-0034-1391345. Epub 2015 Mar 6.
4
Spreading of amyotrophic lateral sclerosis lesions--multifocal hits and local propagation?肌萎缩侧索硬化症病变的扩散——多灶性打击和局部传播?
J Neurol Neurosurg Psychiatry. 2014 Jan;85(1):85-91. doi: 10.1136/jnnp-2013-305617. Epub 2013 Sep 11.
5
Deciphering amyotrophic lateral sclerosis: what phenotype, neuropathology and genetics are telling us about pathogenesis.解析肌萎缩侧索硬化症:表型、神经病理学和遗传学告诉我们发病机制的什么信息。
Amyotroph Lateral Scler Frontotemporal Degener. 2013 May;14 Suppl 1(0 1):5-18. doi: 10.3109/21678421.2013.778548.
6
Electrodiagnosis in persons with amyotrophic lateral sclerosis.肌萎缩侧索硬化症患者的电诊断。
PM R. 2013 May;5(5 Suppl):S89-95. doi: 10.1016/j.pmrj.2013.03.020. Epub 2013 Mar 21.
7
Association of paraspinal and diaphragm denervation in ALS.肌萎缩侧索硬化症中椎旁肌和膈肌去神经支配的关联
Amyotroph Lateral Scler. 2010;11(1-2):63-6. doi: 10.3109/17482960902730080.
8
Paraspinal and limb motor neuron involvement within homologous spinal segments in ALS.肌萎缩侧索硬化症中同源脊髓节段内的椎旁和肢体运动神经元受累情况。
Clin Neurophysiol. 2008 Jul;119(7):1607-13. doi: 10.1016/j.clinph.2008.03.014. Epub 2008 May 8.
9
Implications of ALS focality: rostral-caudal distribution of lower motor neuron loss postmortem.肌萎缩侧索硬化症局灶性的意义:死后下运动神经元损失的头尾分布
Neurology. 2007 May 8;68(19):1576-82. doi: 10.1212/01.wnl.0000261045.57095.56.
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Focality of upper and lower motor neuron degeneration at the clinical onset of ALS.肌萎缩侧索硬化症临床发病时上下运动神经元变性的局灶性
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肌萎缩侧索硬化症患者腹直肌去神经支配与通气功能障碍之间的关联

Association Between Rectus Abdominis Denervation and Ventilation Dysfunction in Patients with Amyotrophic Lateral Sclerosis.

作者信息

Zhang Hua-Gang, Zhang Shuo, Xu Ying-Sheng, Zhang Nan, Fan Dong-Sheng

机构信息

Department of Neurology, Peking University Third Hospital, Beijing 100191, China.

出版信息

Chin Med J (Engl). 2016 Sep 5;129(17):2063-6. doi: 10.4103/0366-6999.189070.

DOI:10.4103/0366-6999.189070
PMID:27569232
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5009589/
Abstract

BACKGROUND

Spontaneous potentials in electromyography (EMG) of paraspinal muscles are associated with diaphragm denervation and, therefore, poor respiratory function in amyotrophic lateral sclerosis (ALS) is understandable. EMG changes in the rectus abdominis (RA) display an effect similar to those in paraspinal muscles with respect to the function of lower motor neurons in the thoracic spinal cord. The RA denervation was examined to determine its association with ventilation dysfunction in ALS.

METHODS

We collected the clinical data of 128 patients with sporadic ALS in Department of Neurology of Peking University Third Hospital from 2009 to 2013. EMG, Revised ALS Functional Rating Scale (ALSFRS-R) and forced vital capacity (FVC) were performed in all patients and the differences in the EMG changes in RA between those with and without FVC ≥ 80% were analysed.

RESULTS

The mean FVC value was 83.4% ± 17.1% (range: 45%-131%) of the predicted value. A total of 79 patients displayed FVC ≥80%, and 49 patients displayed FVC <80%. Compared with the patients displaying a normal FVC (60/79, 75.9%), spontaneous activity in RA was significantly different among those patients displaying an FVC <80% (47/49, 95.9%). In addition, spontaneous potentials in RA were more frequently detected in patients exhibiting dyspnea (32/33, 97.0%) than in patients without dyspnea (75/95, 78.9%).

CONCLUSION

Spontaneous potentials in RA are associated with ventilation dysfunction and dyspnea in ALS patients.

摘要

背景

椎旁肌肌电图(EMG)中的自发电位与膈肌失神经支配有关,因此,肌萎缩侧索硬化症(ALS)患者呼吸功能不佳是可以理解的。腹直肌(RA)的肌电图变化在胸段脊髓下运动神经元功能方面显示出与椎旁肌类似的效应。对RA失神经支配进行检查以确定其与ALS患者通气功能障碍的关系。

方法

我们收集了2009年至2013年北京大学第三医院神经内科128例散发性ALS患者的临床资料。对所有患者进行肌电图、修订的ALS功能评定量表(ALSFRS-R)和用力肺活量(FVC)检查,并分析FVC≥80%和FVC<80%的患者之间RA肌电图变化的差异。

结果

FVC的平均数值为预测值的83.4%±17.1%(范围:45%-131%)。共有79例患者FVC≥80%,49例患者FVC<80%。与FVC正常的患者(60/79,75.9%)相比,FVC<80%的患者(47/49,95.9%)中RA的自发电活动有显著差异。此外,有呼吸困难的患者(32/33,97.0%)比无呼吸困难的患者(75/95,78.9%)更频繁地检测到RA中的自发电位。

结论

RA中的自发电位与ALS患者的通气功能障碍和呼吸困难有关。