Voorhees A P, Jan N-J, Sigal I A
Department of Ophthalmology, UPMC Eye Center, Eye and Ear Institute, Ophthalmology and Visual Science Research Center University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
Department of Ophthalmology, UPMC Eye Center, Eye and Ear Institute, Ophthalmology and Visual Science Research Center University of Pittsburgh School of Medicine, Pittsburgh, PA, USA; Department of Bioengineering, Swanson School of Engineering, University of Pittsburgh, Pittsburgh, PA, USA.
Acta Biomater. 2017 Aug;58:278-290. doi: 10.1016/j.actbio.2017.05.042. Epub 2017 May 18.
It is widely considered that intraocular pressure (IOP)-induced deformation within the neural tissue pores of the lamina cribrosa (LC) contributes to neurodegeneration and glaucoma. Our goal was to study how the LC microstructure and mechanical properties determine the mechanical insult to the neural tissues within the pores of the LC. Polarized light microscopy was used to measure the collagen density and orientation in histology sections of three sheep optic nerve heads (ONH) at both mesoscale (4.4μm) and microscale (0.73μm) resolutions. Mesoscale fiber-aware FE models were first used to calculate ONH deformations at an IOP of 30mmHg. The results were then used as boundary conditions for microscale models of LC regions. Models predicted large insult to the LC neural tissues, with 95th percentile 1st principal strains ranging from 7 to 12%. Pores near the scleral boundary suffered significantly higher stretch compared to pores in more central regions (10.0±1.4% vs. 7.2±0.4%; p=0.014; mean±SD). Variations in material properties altered the minimum, median, and maximum levels of neural tissue insult but largely did not alter the patterns of pore-to-pore variation, suggesting these patterns are determined by the underlying structure and geometry of the LC beams and pores. To the best of our knowledge, this is the first computational model that reproduces the highly heterogeneous neural tissue strain fields observed experimentally.
The loss of visual function associated with glaucoma has been attributed to sustained mechanical insult to the neural tissues of the lamina cribrosa due to elevated intraocular pressure. Our study is the first computational model built from specimen-specific tissue microstructure to consider the mechanics of the neural tissues of the lamina separately from the connective tissue. We found that the deformation of the neural tissue was much larger than that predicted by any recent microstructure-aware models of the lamina. These results are consistent with recent experimental data and the highest deformations were found in the region of the lamina where glaucomatous damage first occurs. This study provides new insight into the complex biomechanical environment within the lamina.
人们普遍认为,眼压(IOP)引起的筛板(LC)神经组织孔隙内的变形会导致神经退行性变和青光眼。我们的目标是研究LC的微观结构和力学性能如何决定对LC孔隙内神经组织的机械损伤。使用偏振光显微镜在中尺度(4.4μm)和微观尺度(0.73μm)分辨率下测量三只绵羊视神经乳头(ONH)组织学切片中的胶原密度和取向。首先使用中尺度纤维感知有限元模型计算眼压为30mmHg时的ONH变形。然后将结果用作LC区域微观尺度模型的边界条件。模型预测对LC神经组织有较大损伤,第95百分位数的第一主应变范围为7%至12%。与更中心区域的孔隙相比,巩膜边界附近的孔隙受到的拉伸明显更高(10.0±1.4%对7.2±0.4%;p = 0.014;平均值±标准差)。材料特性的变化改变了神经组织损伤的最小值、中位数和最大值水平,但在很大程度上没有改变孔隙间变化的模式,表明这些模式由LC梁和孔隙的基础结构和几何形状决定。据我们所知,这是第一个再现实验观察到的高度异质神经组织应变场的计算模型。
与青光眼相关的视觉功能丧失归因于眼压升高对筛板神经组织的持续机械损伤。我们的研究是第一个基于标本特异性组织微观结构构建的计算模型,将筛板神经组织的力学与结缔组织分开考虑。我们发现神经组织的变形比最近任何关于筛板的微观结构感知模型预测的都要大得多。这些结果与最近的实验数据一致,并且在青光眼损伤首先发生的筛板区域发现了最高变形。这项研究为筛板内复杂的生物力学环境提供了新的见解。