Impact of elevated IOP on lamina cribrosa oxygenation; A combined experimental-computational study on monkeys

Yuankai Lu, Yi Hua, Bingrui Wang, Fugiang Zhong, Andrew Theophanous, Shaharoz Tahir, Po-Yi Lee, Ian A Sigal
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Abstract

Purpose: Our goal is to evaluate how lamina cribrosa (LC) oxygenation is affected by the tissue distortions resulting from elevated IOP. Design: Experimental study on monkeys Subjects: Four healthy monkey eyes with OCT scans with IOP of 10 to 50 mmHg, and then with histological sections of LC. Methods: Since in-vivo LC oxygenation measurement is not yet possible, we used 3D eye-specific numerical models of the LC vasculature which we subjected to experimentally-derived tissue deformations. We reconstructed 3D models of the LC vessel networks of 4 healthy monkey eyes from histological sections. We also obtained in-vivo IOP-induced tissue deformations from a healthy monkey using OCT images and digital volume correlation analysis techniques. The extent that LC vessels distort under a given OCT-derived tissue strain remains unknown. We therefore evaluated two biomechanics-based mapping techniques: cross-sectional and isotropic. The hemodynamics and oxygenations of the four vessel networks were simulated for deformations at several IOPs up to 60mmHg. The results were used to determine the effects of IOP on LC oxygen supply, assorting the extent of tissue mild and severe hypoxia. Main Outcome Measures: IOP-induced deformation, vasculature structure, blood supply, and oxygen supply for LC region Result: IOP-induced deformations reduced LC oxygenation significantly. More than 20% of LC tissue suffered from mild hypoxia when IOP reached 30 mmHg. Extreme IOP(>50mmHg) led to large severe hypoxia regions (>30%) in the isotropic mapping cases. Conclusion: Our models predicted that moderately elevated IOP can lead to mild hypoxia in a substantial part of the LC, which, if sustained chronically, may contribute to neural tissue damage. For extreme IOP elevations, severe hypoxia was predicted, which would potentially cause more immediate damage. Our findings suggest that despite the remarkable LC vascular robustness, IOP-induced distortions can potentially contribute to glaucomatous neuropathy.
眼压升高对肋膜氧合的影响;对猴子进行的实验与计算相结合的研究
目的:我们的目标是评估眼压升高导致的组织变形如何影响颅底薄层(LC)的氧合作用。设计:对猴子进行实验研究:四只健康猴眼在眼压为 10 至 50 mmHg 时进行 OCT 扫描,然后对 LC 进行组织切片检查:由于目前还无法测量活体 LC 含氧量,我们使用了眼球特定的 LC 血管三维数值模型,并对其进行了实验性组织变形。我们根据组织学切片重建了 4 只健康猴眼 LC 血管网络的三维模型。我们还利用 OCT 图像和数字容积相关分析技术获得了一只健康猴子体内 IOP 诱导的组织变形。在给定的 OCT 组织应变下,LC 血管的变形程度仍然未知。因此,我们评估了两种基于生物力学的绘图技术:横截面和各向同性。我们模拟了四种血管网络在不同眼压(最高 60mmHg)下的血液动力学和氧合作用。结果用于确定眼压对 LC 供氧的影响,以及组织轻度和重度缺氧的程度。主要结果指标:眼压引起的变形、血管结构、血液供应和 LC 区域的氧气供应结果:眼压引起的变形显著降低了 LC 的氧合。当眼压达到 30 mmHg 时,超过 20% 的 LC 组织出现轻度缺氧。在各向同性绘图案例中,极高的眼压(>50mmHg)导致大面积严重缺氧(>30%):我们的模型预测,中度升高的眼压会导致 LC 的大部分区域轻度缺氧,如果长期持续,可能会造成神经组织损伤。对于极端的眼压升高,预测会出现严重缺氧,这可能会造成更直接的损害。我们的研究结果表明,尽管低眼压区血管具有显著的稳健性,但由眼压引起的扭曲有可能导致青光眼神经病变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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