Tavakoli Mitra, Malik Rayaz A
Division of Cardiovascular Medicine, University of Manchester.
J Vis Exp. 2011 Jan 3(47):2194. doi: 10.3791/2194.
The accurate quantification of peripheral neuropathy is important to define at risk patients, anticipate deterioration, and assess new therapies. Conventional methods assess neurological deficits and electrophysiology and quantitative sensory testing quantifies functional alterations to detect neuropathy. However, the earliest damage appears to be to the small fibres and yet these tests primarily assess large fibre dysfunction and have a limited ability to demonstrate regeneration and repair. The only techniques which allow a direct examination of unmyelinated nerve fibre damage and repair are sural nerve biopsy with electron microscopy and skin-punch biopsy. However, both are invasive procedures and require lengthy laboratory procedures and considerable expertise. Corneal Confocal microscopy is a non-invasive clinical technique which provides in-vivo imaging of corneal nerve fibres. We have demonstrated early nerve damage, which precedes loss of intraepidermal nerve fibres in skin biopsies together with stratification of neuropathic severity and repair following pancreas transplantation in diabetic patients. We have also demonstrated nerve damage in idiopathic small fibre neuropathy and Fabry's disease.
准确量化周围神经病变对于确定高危患者、预测病情恶化以及评估新疗法至关重要。传统方法评估神经功能缺损、电生理学,而定量感觉测试则量化功能改变以检测神经病变。然而,最早的损伤似乎发生在小纤维,但这些测试主要评估大纤维功能障碍,且在显示神经再生和修复方面能力有限。唯一能够直接检查无髓神经纤维损伤和修复的技术是腓肠神经活检(结合电子显微镜)和皮肤打孔活检。然而,这两种都是侵入性操作,需要漫长的实验室流程和相当专业的知识。角膜共聚焦显微镜检查是一种非侵入性临床技术,可提供角膜神经纤维的体内成像。我们已经证明,在糖尿病患者胰腺移植后,早期神经损伤先于皮肤活检中表皮内神经纤维的丧失,同时伴有神经病变严重程度的分层和修复。我们还在特发性小纤维神经病变和法布里病中证明了神经损伤。