Kallinikos Panagiotis, Efron Nathan
Eurolens Research, Department of Optometry and Neuroscience, University of Manchester Institute of Science and Technology, Manchester, United Kingdom.
Invest Ophthalmol Vis Sci. 2004 Sep;45(9):3011-20. doi: 10.1167/iovs.04-0129.
To employ confocal microscopy to investigate the etiology of keratocyte loss after short-term contact lens wear by monitoring quantitative changes in keratocyte density.
Twenty neophyte subjects aged 26 +/- 3 years participated in the study, which was conducted over the course of three experimental sessions. In the first session, one eye of each subject was fitted with a silicone hydrogel contact lens, and the other eye served as the control. Both corneas were exposed to an anoxic environment for 2 hours. Ultrasound pachometry and confocal microscopy were performed on both eyes at baseline, immediately after the experiment and 2 hours post experiment. This procedure was repeated after 72 hours, but in this case one eye of each subject was fitted with a hyper-Dk rigid contact lens, and the fellow eye served again as the control. In the third experimental session, each subject was asked to periodically rub one eye only. Tear samples collected from the rubbed and control eyes were assayed for epidermal growth factor (EGF), hepatocyte growth factor (HGF), and interleukin (IL)-8.
The increase in corneal thickness was similar in the experimental and control eyes. Both anterior and posterior keratocyte densities decreased in the experimental eyes compared with the control eyes, in all sessions. EGF and IL-8 concentrations were increased in the rubbed eyes compared with the control eyes.
It is hypothesized that the mechanical stimulation of the corneal surface, due to the physical presence of a contact lens, induces the release of inflammatory mediators that cause keratocyte dysgenesis or apoptosis.
通过监测角膜细胞密度的定量变化,利用共聚焦显微镜研究短期佩戴隐形眼镜后角膜细胞丢失的病因。
20名年龄在26±3岁的初戴者参与了该研究,研究在三个实验阶段进行。在第一阶段,每个受试者的一只眼睛佩戴硅水凝胶隐形眼镜,另一只眼睛作为对照。两只角膜均暴露于缺氧环境2小时。在基线、实验结束后立即以及实验后2小时对两只眼睛进行超声角膜测厚和共聚焦显微镜检查。72小时后重复此过程,但在这种情况下,每个受试者的一只眼睛佩戴高透氧性硬性隐形眼镜,另一只眼睛再次作为对照。在第三个实验阶段,要求每个受试者仅定期揉搓一只眼睛。对从揉搓眼和对照眼中收集的泪液样本检测表皮生长因子(EGF)、肝细胞生长因子(HGF)和白细胞介素(IL)-8。
实验眼和对照眼角膜厚度的增加相似。在所有阶段,与对照眼相比,实验眼前、后角膜细胞密度均降低。与对照眼相比,揉搓眼中EGF和IL-8浓度升高。
据推测,由于隐形眼镜的物理存在,角膜表面受到的机械刺激会诱导炎症介质的释放,从而导致角膜细胞发育异常或凋亡。