Kim Yong Woo, Jeoung Jin Wook, Kim Young Kook, Park Ki Ho
*Department of Ophthalmology, Armed Forces Capital Hospital, Seongnam, Korea †Department of Ophthalmology, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea.
J Glaucoma. 2017 Sep;26(9):753-761. doi: 10.1097/IJG.0000000000000728.
The lamina cribrosa (LC) is a multilayered, collagenous, sieve-like structure at the deep optic nerve head, and is presumed to be the primary site of axonal injury. According to biomechanical theory, intraocular pressure-induced posterior deformation of the LC causes blockage of axonal transport and alters the ocular blood flow, so that the axons of the retinal ganglion cells lead to apoptosis, which results in glaucomatous optic disc change. Although most of the research on the LC to date has been limited to experimental animal or histologic studies, the recent advances in optical coherence tomography devices and image processing techniques have made possible the visualization of the LC structure in vivo. LC deformation in glaucoma typically has been evaluated in terms of its position from a structural reference plane (LC depth), entire curvature or shape, thickness, or localized structural change (focal LC defects or LC pore change). In this review, we highlight the methods of assessing LC deformation from in vivo optical coherence tomography scans, and we discuss the clinical implications of the recent investigations of the in vivo structure of LC in glaucoma.
筛板(LC)是位于视神经乳头深部的多层胶原筛状结构,被认为是轴突损伤的主要部位。根据生物力学理论,眼内压引起的筛板后移会导致轴突运输受阻并改变眼部血流,从而使视网膜神经节细胞的轴突发生凋亡,进而导致青光眼性视盘改变。尽管目前关于筛板的大多数研究仅限于实验动物或组织学研究,但光学相干断层扫描设备和图像处理技术的最新进展已使在体观察筛板结构成为可能。青光眼患者的筛板变形通常根据其相对于结构参考平面的位置(筛板深度)、整体曲率或形状、厚度或局部结构变化(局灶性筛板缺损或筛板孔隙变化)来评估。在本综述中,我们重点介绍了通过活体光学相干断层扫描评估筛板变形的方法,并讨论了近期青光眼患者筛板活体结构研究的临床意义。