Yorek Matthew S, Davidson Eric P, Poolman Pieter, Coppey Lawrence J, Obrosov Alexander, Holmes Amey, Kardon Randy H, Yorek Mark A
Department of Veterans Affairs Iowa City Health Care System, Iowa City, Iowa, United States 2Veterans Affairs Center for the Prevention and Treatment of Visual Loss, Iowa City, Iowa, United States.
Department of Internal Medicine, University of Iowa, Iowa City, Iowa, United States.
Invest Ophthalmol Vis Sci. 2016 May 1;57(6):2412-9. doi: 10.1167/iovs.16-19435.
Diagnosis of peripheral neuropathy (PN), which affects approximately 50% of the diabetic population, is subjective, with many patients seeking a diagnosis only after presenting with symptoms. Recently, in vivo confocal microscopy of subepithelial corneal nerve density has been promoted as a surrogate marker for early detection of PN, but imaging of corneal nerves requires sophisticated instrumentation, expertise in confocal imaging, cooperative patients, and automated analysis tools to derive corneal nerve density. As an alternative, we developed a simple screening method that is based on the sensitivity of corneal nerves to cause reflex eyelid squinting in response to hyperosmolar eye drops.
Eyes of control and type 2 diabetic rats were given an eye drop of a 290- to 900-mOsm solution, and the ocular response was video recorded. Other neuropathic end points including nerve conduction velocity and subepithelial cornea nerve density were determined.
Motor and sensory nerve conduction velocity and total nerve fiber length of corneal nerves in the subepithelial layer were significantly decreased in diabetic rats. Applying the hyperosmotic solutions to the ocular surface caused an osmolarity-dependent increase in squinting of the treated eye in control rats. Squinting was almost totally blocked by preapplication of proparacaine or N-(4-tertiarybutylphenyl)-4-(3-chloropyridin-2-yl)tetrahydropyrazine-1(2H)-carbox-amide, a transient receptor potential melastatin-8 channel blocker. Squinting in response to the 900-mOsm solution was significantly reduced in diabetic rats.
Preclinical studies show that evaluation of corneal sensitivity may be an alternative method for the early detection of PN and has potential for translation to clinical studies.
外周神经病变(PN)影响着约50%的糖尿病患者,其诊断具有主观性,许多患者在出现症状后才寻求诊断。近来,上皮下角膜神经密度的体内共聚焦显微镜检查已被推广作为PN早期检测的替代标志物,但角膜神经成像需要精密仪器、共聚焦成像专业知识、配合良好的患者以及用于得出角膜神经密度的自动化分析工具。作为一种替代方法,我们开发了一种基于角膜神经对高渗滴眼液产生反射性眼睑眯眼反应的敏感性的简单筛查方法。
给对照大鼠和2型糖尿病大鼠的眼睛滴入290至900毫渗摩尔溶液,并对眼部反应进行视频记录。测定包括神经传导速度和上皮下角膜神经密度在内的其他神经病变终点指标。
糖尿病大鼠的运动和感觉神经传导速度以及上皮下层角膜神经的总神经纤维长度显著降低。向对照大鼠的眼表应用高渗溶液会导致受试眼的眯眼反应随渗透压升高而增加。预先应用丙美卡因或N-(4-叔丁基苯基)-4-(3-氯吡啶-2-基)四氢吡嗪-1(2H)-甲酰胺(一种瞬时受体电位香草酸亚型8通道阻滞剂)几乎完全阻断了眯眼反应。糖尿病大鼠对900毫渗摩尔溶液的眯眼反应显著降低。
临床前研究表明,评估角膜敏感性可能是早期检测PN的一种替代方法,并且具有转化为临床研究的潜力。