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脊髓性肌萎缩症 2 型和 3 型中神经肌肉接头功能障碍。

Dysfunction of the neuromuscular junction in spinal muscular atrophy types 2 and 3.

机构信息

Department of Neurology, Rudolf Magnus Institute of Neuroscience, University Medical Center Utrecht, Utrecht, the Netherlands.

出版信息

Neurology. 2012 Nov 13;79(20):2050-5. doi: 10.1212/WNL.0b013e3182749eca. Epub 2012 Oct 31.

Abstract

OBJECTIVE

Spinal muscular atrophy (SMA) is pathologically characterized by degeneration of anterior horn cells. Recent observations in animal models of SMA and muscle tissue from patients with SMA suggest additional abnormalities in the development and maturation of the neuromuscular junction. We therefore evaluated neuromuscular junction function in SMA with repetitive nerve stimulation.

METHODS

In this case-control study, repetitive nerve stimulation was performed in 35 patients with SMA types 2, 3, and 4, 20 healthy controls, and 5 controls with motor neuron disease.

RESULTS

Pathologic decremental responses (>10%) during 3-Hz repetitive nerve stimulation were observed in 17 of 35 patients (49%) with SMA types 2 and 3, but not in healthy controls or controls with motor neuron disease. None of the patients or controls had an abnormal incremental response of >60%. The presence of an abnormal decremental response was not specific for the type of SMA, nor was it associated with compound muscle action potential amplitude, clinical scores, or disease duration. Two of 4 patients with SMA type 3 who tried pyridostigmine reported increased stamina.

CONCLUSIONS

These data suggest dysfunction of the neuromuscular junction in patients with SMA types 2 and 3. Therefore, drugs that facilitate neuromuscular transmission are candidate drugs for evaluation in carefully designed, placebo-controlled, clinical trials.

摘要

目的

脊髓性肌萎缩症(SMA)在病理学上表现为前角细胞退化。最近在 SMA 动物模型和 SMA 患者的肌肉组织中的观察结果表明,神经肌肉接头在发育和成熟方面存在其他异常。因此,我们使用重复神经刺激来评估 SMA 中的神经肌肉接头功能。

方法

在这项病例对照研究中,对 35 名 SMA 2 型、3 型和 4 型患者、20 名健康对照者和 5 名运动神经元病对照者进行了重复神经刺激。

结果

在 17 名 SMA 2 型和 3 型患者(49%)中观察到 3Hz 重复神经刺激期间出现病理性递减反应(>10%),但在健康对照者或运动神经元病对照者中未观察到。患者或对照者均未出现>60%的异常递增反应。异常递减反应的存在不仅不是 SMA 类型的特异性,也与复合肌肉动作电位幅度、临床评分或疾病持续时间无关。尝试吡啶斯的明的 4 名 SMA 3 型患者中有 2 名报告耐力增加。

结论

这些数据表明 SMA 2 型和 3 型患者的神经肌肉接头功能障碍。因此,促进神经肌肉传递的药物是在精心设计的、安慰剂对照的临床试验中进行评估的候选药物。

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