Grytz Rafael, Yang Hongli, Hua Yi, Samuels Brian C, Sigal Ian A
Department of Ophthalmology and Visual Sciences, University of Alabama at Birmingham, Birmingham, Alabama, United States.
Devers Eye Institute, Legacy Health System, Portland, Oregon, United States.
Curr Opin Biomed Eng. 2020 Sep;15:40-50. doi: 10.1016/j.cobme.2020.01.001. Epub 2020 Jan 28.
Myopia and glaucoma are both increasing in prevalence and are linked by an unknown mechanism as many epidemiologic studies have identified moderate to high myopia as an independent risk factor for glaucoma. Myopia and glaucoma are both chronic conditions that lead to connective tissue remodeling within the sclera and optic nerve head. The mechanobiology underlying connective tissue remodeling differs substantially between both diseases, with different homeostatic control mechanisms. In this article, we discuss similarities and differences between connective tissue remodeling in myopia and glaucoma; selected multi-scale mechanisms that are thought to underlie connective tissue remodeling in both conditions; how asymmetric remodeling of the optic nerve head may predispose a myopic eye for pathological remodeling and glaucoma; and how neural tissue deformations may accumulate throughout both pathologies and increase the risk for mechanical insult of retinal ganglion cell axons.
近视和青光眼的患病率均在上升,并且通过一种未知机制相互关联,因为许多流行病学研究已将中度至高度近视确定为青光眼的独立危险因素。近视和青光眼都是慢性病,会导致巩膜和视神经乳头内的结缔组织重塑。两种疾病中结缔组织重塑背后的力学生物学有很大差异,具有不同的稳态控制机制。在本文中,我们讨论了近视和青光眼中结缔组织重塑的异同;被认为是这两种情况下结缔组织重塑基础的选定多尺度机制;视神经乳头的不对称重塑如何使近视眼易于发生病理性重塑和青光眼;以及神经组织变形如何在两种病理过程中积累并增加视网膜神经节细胞轴突受到机械损伤的风险。