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肌萎缩患者的运动单位数量指数(MUNIX)。

The Motor Unit Number Index (MUNIX) in sarcopenic patients.

机构信息

Universität Erlangen-Nürnberg, Institute for Biomedicine of Aging, Heimerichstrasse 58, 90419 Nuremberg, Germany.

出版信息

Exp Gerontol. 2013 Apr;48(4):381-4. doi: 10.1016/j.exger.2013.01.011. Epub 2013 Jan 31.

Abstract

INTRODUCTION

The cause of sarcopenia is still not fully understood. A multifactorial aetiology is discussed. Neurodegenerative aspects in the genesis of sarcopenia, such as loss of motoneurons, have not yet been explored to a sufficient extent.

METHOD

The Motor Unit Number Index (MUNIX) is a method for assessing the number and size (Motor Unit Size Index - MUSIX) of Motor Units (MUs) using the Compound Muscle Action Potential (CMAP) and the Surface electromyographic Interference Pattern (SIP). This method was used to study the hypothenar muscle in the right hand of 27 sarcopenic patients.

RESULTS

The mean MUNIX (111±51) of all investigated sarcopenic patients lies between the mean MUNIX of healthy persons and the mean MUNIX of ALS patients. 25% of sarcopenic patients exhibit pathologic values for both MUNIX (<80) and MUSIX (>100 μV). A strong correlation (r=0.75, p<0.001) between MUSIX and the reciprocal value of MUNIX was identified.

CONCLUSION

It was demonstrated for the first time by applying the MUNIX technique that loss of motoneurons plays a pathogenic role in the onset of sarcopenia. This was shown in 25% of sarcopenic participants who exhibited pathologic values for both MUNIX and MUSIX. Nerve sprouting seems to be an important mechanism of compensation for loss of motoneurons, reflected by the strong correlation between MUNIX and MUSIX. Use of MUNIX leads to the identification of a distinct subgroup of sarcopenic patients, which might have a major impact on future diagnostic and therapeutic concepts.

摘要

简介

肌少症的病因仍不完全清楚。目前讨论其多因素病因。神经退行性方面在肌少症的发生中,如运动神经元的丧失,尚未得到充分的探索。

方法

运动单位数量指数(MUNIX)是一种使用复合肌肉动作电位(CMAP)和表面肌电图干扰图案(SIP)评估运动单位(MU)数量和大小(运动单位大小指数 - MUSIX)的方法。该方法用于研究 27 例肌少症患者右手小鱼际肌。

结果

所有研究的肌少症患者的平均 MUNIX(111±51)介于健康人和肌萎缩侧索硬化症患者的平均 MUNIX 之间。25%的肌少症患者的 MUNIX(<80)和 MUSIX(>100 μV)均出现病理值。MUSIX 和 MUNIX 的倒数之间存在很强的相关性(r=0.75,p<0.001)。

结论

首次通过应用 MUNIX 技术证明运动神经元的丧失在肌少症的发病中起致病作用。25%的肌少症患者的 MUNIX 和 MUSIX 均出现病理值。神经发芽似乎是运动神经元丧失的重要代偿机制,MUNIX 和 MUSIX 之间的强相关性反映了这一点。使用 MUNIX 可识别出一个明显的肌少症患者亚组,这可能对未来的诊断和治疗概念产生重大影响。

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