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脊髓性肌萎缩症和脊髓延髓肌萎缩症中明显的疲劳:与活动相关的传导阻滞的证据。

Prominent fatigue in spinal muscular atrophy and spinal and bulbar muscular atrophy: evidence of activity-dependent conduction block.

机构信息

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

出版信息

Clin Neurophysiol. 2013 Sep;124(9):1893-8. doi: 10.1016/j.clinph.2012.12.053. Epub 2013 Apr 30.

Abstract

OBJECTIVES

To clarify whether patients with spinal muscular atrophy (SMA) or spinal and bulbar muscular atrophy (SBMA) suffer disabling muscle fatigue, and whether activity-dependent conduction block (ADCB) contributes to their fatigue. ADCB is usually caused by reduced safety factor for impulse transmission in demyelinating diseases, whereas markedly increased axonal branching associated with collateral sprouting may reduce the safety factor in chronic lower motor neuron disorders.

METHODS

We assessed the fatigue severity scale (FSS) in 22 patients with SMA/SBMA, and in 100 disease controls (multiple sclerosis, myasthenia gravis, chronic inflammatory demyelinating polyneuropathy (CIDP), and axonal neuropathy). We then performed stimulated-single fibre electromyography (s-SFEMG) in the extensor digitorum communis (EDC) muscle of 21 SMA/SBMA patients, 6 CIDP patients, and 10 normal subjects.

RESULTS

The FSS score was the highest in SMA/SBMA patients [4.9 ± 1.1 (mean ± SD)], with 81% of them complaining of disabling fatigue, compared with normal controls (3.5 ± 1.0), whereas patients with multiple sclerosis (4.3 ± 1.6), myasthenia gravis (4.0 ± 1.6) or CIDP (4.3 ± 1.4) also showed higher FSS score. When 2000 stimuli were delivered at 20 Hz in s-SFEMG, conduction block of single motor axons developed in 46% of patients with SMA/SBMA, and 40% of CIDP patients, but in none of the normal controls.

CONCLUSION

SMA/SBMA patients frequently suffer from disabling fatigue presumably caused by ADCB induced by voluntary activity.

SIGNIFICANCE

ADCB could be the mechanism for muscle fatigue in chronic lower motor neuron diseases.

摘要

目的

阐明脊髓性肌萎缩症(SMA)或脊髓延髓肌萎缩症(SBMA)患者是否存在致残性肌肉疲劳,以及活动依赖性传导阻滞(ADCB)是否导致其疲劳。ADCB 通常是由脱髓鞘疾病中冲动传递的安全系数降低引起的,而与侧支发芽相关的轴突分支显著增加可能会降低慢性下运动神经元疾病中的安全系数。

方法

我们评估了 22 例 SMA/SBMA 患者和 100 例疾病对照组(多发性硬化症、重症肌无力、慢性炎症性脱髓鞘性多发性神经病(CIDP)和轴索性神经病)的疲劳严重程度量表(FSS)。然后,我们在 21 例 SMA/SBMA 患者、6 例 CIDP 患者和 10 例正常对照者的伸指总肌中进行了刺激单纤维肌电图(s-SFEMG)。

结果

SMA/SBMA 患者的 FSS 评分最高[4.9±1.1(平均值±标准差)],81%的患者抱怨存在致残性疲劳,而正常对照组为 3.5±1.0,多发性硬化症患者(4.3±1.6)、重症肌无力患者(4.0±1.6)或 CIDP 患者(4.3±1.4)的 FSS 评分也较高。当在 s-SFEMG 中以 20Hz 施加 2000 次刺激时,46%的 SMA/SBMA 患者和 40%的 CIDP 患者出现单个运动轴突的传导阻滞,但在正常对照组中均未出现。

结论

SMA/SBMA 患者常因自愿活动引起的 ADCB 而遭受致残性疲劳。

意义

ADCB 可能是慢性下运动神经元疾病肌肉疲劳的机制。

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