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From the bedside to the bench and back again, with corneal confocal microscopy

机译:使用角膜共聚焦显微镜从床头到长凳再返回

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摘要

In this issue of IOVS, Davidson and colleagues1 apply a range of conventional techniques and the novel ophthalmic technique of corneal confocal microscopy (CCM) to phenotype nerve damage in an experimental model of prediabetes and type 2 diabetes. The key findings are that CCM allows a noninvasive demonstration of an early reduction in corneal innervation that correlates with a reduction in both corneal and intraepidermal nerve fiber density derived using invasive corneal and skin biopsy and conventional tissue histology. These abnormalities occur in parallel with a reduction in corneal sensitivity and conventionally accepted end points of thermal nociception latency and sensory nerve conduction velocity. These data build on the concept that CCM allows the rapid, noninvasive, and hence reiterative study of corneal nerves in a variety of animal species,2 and in particular in the diagnosis and assessment of therapeutic efficacy in experimental diabetes3,4 and patients with diabetic neuropathy.5,6
机译:在本期IOVS中,Davidson及其同事1在糖尿病前期和2型糖尿病的实验模型中,应用了一系列常规技术和角膜共聚焦显微镜(CCM)的新型眼科技术来对表型神经进行损伤。关键发现是CCM可以无创地证明角膜神经支配的早期减少,这与使用侵入性角膜和皮肤活检以及常规组织组织学方法得出的角膜和表皮内神经纤维密度的减少有关。这些异常与角膜敏感性的降低以及热伤害感受潜伏期和感觉神经传导速度的常规接受的终点降低同时发生。这些数据建立在以下概念的基础上:CCM可以对各种动物物种进行角膜神经的快速,无创且因此重复的研究2,尤其是在实验性糖尿病3、4和糖尿病性神经病患者的诊断和疗效评估中.5,6

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