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肌萎缩侧索硬化症感觉异常的临床、电生理及病理证据

Clinical, electrophysiologic, and pathologic evidence for sensory abnormalities in ALS.

作者信息

Hammad M, Silva A, Glass J, Sladky J T, Benatar M

机构信息

Department of Neurology, Emory University, Woodruff Memorial Building, 101 Woodruff Circle, Atlanta, GA 30322, USA.

出版信息

Neurology. 2007 Dec 11;69(24):2236-42. doi: 10.1212/01.wnl.0000286948.99150.16.

Abstract

BACKGROUND

Amyotrophic lateral sclerosis (ALS) is a progressive degenerative disease of upper and lower motor neurons. Reports of the nature and frequency of sensory nerve involvement in ALS have varied.

METHODS

We reviewed the Emory University motor neuron disease registry between 1997 and 2004 to identify 103 patients with ALS without coexisting diseases that might cause sensory abnormalities and for whom electrodiagnostic studies were available for review. Neurophysiologic studies were interpreted based on age-adjusted normative data from our laboratory. Twelve control biopsies were evaluated alongside 22 samples from patients with ALS to ensure blinded evaluation of pathologic specimens.

RESULTS

Sensory symptoms or signs were present in 32% of patients, sural sensory nerve action potential amplitudes were abnormal in 27%, and pathologic abnormalities were present in 91% of patients. Large-caliber myelinated fibers were predominantly affected (reduced in 73%) and small-caliber myelinated fibers were affected less often (23%). Thinly myelinated fibers were present in 95% and regenerating clusters in 77% of the biopsies. Teased fiber analysis showed an increased frequency of axonal degeneration and regeneration as well as excessive myelin irregularity. Morphometry confirmed the loss of large-caliber fibers.

CONCLUSIONS

These data indicate that one third of patients with amyotrophic lateral sclerosis report sensory symptoms and sural sensory response amplitudes are reduced in a similar proportion of subjects. Pathologic evidence of sensory nerve pathology was present in 91% of patients who underwent sural nerve biopsy. The electrophysiologic and pathologic findings indicate a pattern of axonal loss that predominantly affects large-caliber myelinated fibers.

摘要

背景

肌萎缩侧索硬化症(ALS)是一种上下运动神经元的进行性退行性疾病。关于ALS中感觉神经受累的性质和频率的报道各不相同。

方法

我们回顾了1997年至2004年埃默里大学运动神经元疾病登记处的数据,以确定103例无可能导致感觉异常的共存疾病且有可用电诊断研究以供审查的ALS患者。神经生理学研究根据我们实验室的年龄校正规范数据进行解读。对12例对照活检样本和22例ALS患者的样本进行评估,以确保对病理标本进行盲法评估。

结果

32%的患者存在感觉症状或体征,27%的患者腓肠感觉神经动作电位幅度异常,91%的患者存在病理异常。大口径有髓纤维主要受累(73%减少),小口径有髓纤维受累较少(23%)。95%的活检样本中存在薄髓纤维,77%的样本中存在再生簇。单纤维分析显示轴突变性和再生频率增加以及髓鞘过度不规则。形态计量学证实了大口径纤维的丢失。

结论

这些数据表明,三分之一的肌萎缩侧索硬化症患者报告有感觉症状,且类似比例的受试者腓肠感觉反应幅度降低。91%接受腓肠神经活检的患者存在感觉神经病理的证据。电生理和病理结果表明存在一种主要影响大口径有髓纤维的轴突丢失模式。

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