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本文引用的文献

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Age- and race-related differences in human scleral material properties.人类巩膜材料特性的年龄和种族差异。
Invest Ophthalmol Vis Sci. 2014 Nov 11;55(12):8163-72. doi: 10.1167/iovs.14-14029.
2
Factors affecting plastic lamina cribrosa displacement in glaucoma patients.影响青光眼患者筛板层移位的因素。
Invest Ophthalmol Vis Sci. 2014 Nov 4;55(12):7709-15. doi: 10.1167/iovs.14-13957.
3
Human scleral structural stiffness increases more rapidly with age in donors of African descent compared to donors of European descent.与欧洲裔捐献者相比,非洲裔捐献者的人类巩膜结构硬度随年龄增长的速度更快。
Invest Ophthalmol Vis Sci. 2014 Sep 18;55(11):7189-98. doi: 10.1167/iovs.14-14894.
4
In vivo three-dimensional characterization of the healthy human lamina cribrosa with adaptive optics spectral-domain optical coherence tomography.利用自适应光学光谱域光学相干断层扫描对健康人筛板进行体内三维表征。
Invest Ophthalmol Vis Sci. 2014 Sep 16;55(10):6459-66. doi: 10.1167/iovs.14-15177.
5
Longitudinal alterations in the dynamic autoregulation of optic nerve head blood flow revealed in experimental glaucoma.实验性青光眼中视神经头血流的动态自身调节的纵向改变。
Invest Ophthalmol Vis Sci. 2014 May 8;55(6):3509-16. doi: 10.1167/iovs.14-14020.
6
Optic neuropathy induced by experimentally reduced cerebrospinal fluid pressure in monkeys.实验性降低脑脊液压力诱发猴子视神经病变
Invest Ophthalmol Vis Sci. 2014 Apr 15;55(5):3067-73. doi: 10.1167/iovs.13-13657.
7
The role of matricellular proteins in glaucoma.基质细胞蛋白在青光眼发病机制中的作用
Matrix Biol. 2014 Jul;37:174-82. doi: 10.1016/j.matbio.2014.03.007. Epub 2014 Apr 12.
8
Scleral permeability varies by mouse strain and is decreased by chronic experimental glaucoma.巩膜通透性因小鼠品系而异,并可被慢性实验性青光眼所降低。
Invest Ophthalmol Vis Sci. 2014 Apr 21;55(4):2564-73. doi: 10.1167/iovs.13-13327.
9
Susceptibility to glaucoma damage related to age and connective tissue mutations in mice.小鼠青光眼损伤易感性与年龄和结缔组织突变有关。
Exp Eye Res. 2014 Feb;119:54-60. doi: 10.1016/j.exer.2013.12.008. Epub 2013 Dec 22.
10
Biomechanics of the posterior eye: a critical role in health and disease.眼球后部的生物力学:在健康与疾病中起关键作用。
J Biomech Eng. 2014 Feb;136(2):021005. doi: 10.1115/1.4026286.

衰老与疾病中的视神经乳头生物力学

Optic nerve head biomechanics in aging and disease.

作者信息

Downs J Crawford

机构信息

Department of Ophthalmology, University of Alabama at Birmingham School of Medicine, 1670 University Blvd., VH 390A, Birmingham, AL 35294, USA.

出版信息

Exp Eye Res. 2015 Apr;133:19-29. doi: 10.1016/j.exer.2015.02.011.

DOI:10.1016/j.exer.2015.02.011
PMID:25819451
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4379445/
Abstract

This nontechnical review is focused upon educating the reader on optic nerve head biomechanics in both aging and disease along two main themes: what is known about how mechanical forces and the resulting deformations are distributed in the posterior pole and ONH (biomechanics) and what is known about how the living system responds to those deformations (mechanobiology). We focus on how ONH responds to IOP elevations as a structural system, insofar as the acute mechanical response of the lamina cribrosa is confounded with the responses of the peripapillary sclera, prelaminar neural tissues, and retrolaminar optic nerve. We discuss the biomechanical basis for IOP-driven changes in connective tissues, blood flow, and cellular responses. We use glaucoma as the primary framework to present the important aspects of ONH biomechanics in aging and disease, as ONH biomechanics, aging, and the posterior pole extracellular matrix (ECM) are thought to be centrally involved in glaucoma susceptibility, onset and progression.

摘要

本非技术性综述旨在围绕两个主要主题,向读者介绍衰老和疾病状态下的视神经乳头生物力学:一是关于机械力及其产生的变形如何在后极部和视神经乳头(ONH)分布的已知情况(生物力学);二是关于生命系统如何对这些变形作出反应的已知情况(力学生物学)。我们关注视神经乳头作为一个结构系统如何对眼压升高作出反应,因为筛板的急性机械反应与视乳头周围巩膜、板前神经组织和板后视神经的反应相互混淆。我们讨论了眼压驱动的结缔组织、血流和细胞反应变化的生物力学基础。我们以青光眼作为主要框架,来阐述衰老和疾病状态下视神经乳头生物力学的重要方面,因为视神经乳头生物力学、衰老和后极部细胞外基质(ECM)被认为在青光眼易感性、发病和进展中起着核心作用。