Department of Neuroscience, Neurological Clinic, University of Pisa, Via Roma 67, 56126 Pisa, Italy.
Neurol Sci. 2012 Apr;33(2):449-52. doi: 10.1007/s10072-011-0703-4. Epub 2011 Jul 13.
Involvement of the peripheral nervous system in mitochondrial disorders (MD) has been previously reported. However, the exact prevalence of peripheral neuropathy and/or myopathy in MD is still unclear. In order to evaluate the prevalence of neuropathy and myopathy in MD, we performed sensory and motor nerve conduction studies (NCS) and concentric needle electromyography (EMG) in 44 unselected MD patients. NCS were abnormal in 36.4% of cases, and were consistent with a sensori-motor axonal multineuropathy (multifocal neuropathy), mainly affecting the lower limbs. EMG evidence of myopathy was present in 54.5% of patients, again mainly affecting the lower limbs. Nerve and muscle involvement was frequently subclinical. Peripheral nerve and muscle involvement is common in MD patients. Our study supports the variability of the clinical expression of MD. Further studies are needed to better understand the molecular basis underlying the phenotypic variability among MD patients.
先前已有报告指出,周围神经系统会牵涉到线粒体疾病(MD)中。然而,确切的周围神经病变和/或肌病在 MD 中的患病率仍不清楚。为了评估 MD 中神经病和肌病的患病率,我们对 44 名未经选择的 MD 患者进行了感觉和运动神经传导研究(NCS)和同心针肌电图(EMG)检查。36.4%的病例出现 NCS 异常,且与感觉运动性轴索性多发性神经病(多灶性神经病)一致,主要影响下肢。54.5%的患者出现肌病的 EMG 证据,同样主要影响下肢。神经和肌肉的受累通常是亚临床的。周围神经和肌肉的受累在 MD 患者中很常见。我们的研究支持 MD 临床表现的可变性。需要进一步的研究来更好地了解 MD 患者表型变异性的分子基础。