Singapore Eye Research Institute (SERI), Singapore National Eye Centre (SNEC), Singapore, Singapore.
Singapore-MIT Alliance for Research and Technology, Singapore, Singapore.
Biomech Model Mechanobiol. 2024 Dec;23(6):2137-2154. doi: 10.1007/s10237-024-01885-9. Epub 2024 Sep 25.
The purpose of this study was to assess whether growth and remodeling (G&R) theory could explain staphyloma formation from a local scleral weakening-as could occur from age-related elastin degradation, myopia progression, or other factors. A finite element model of a healthy eye was reconstructed, including the lamina cribrosa, the peripapillary sclera, and the peripheral sclera. The homogenized constrained mixture model was employed to simulate the adaptation of the sclera to alterations in its biomechanical environment over a duration of 13.7 years. G&R processes were triggered by reducing the shear stiffness of the ground matrix in the peripapillary sclera and lamina cribrosa by 85%. Three distinct G&R scenarios were investigated: (1) low mass turnover rate in combination with transmural volumetric growth; (2) high mass turnover rate in combination with transmural volumetric growth; and (3) high mass turnover rate in combination with mass density growth. In scenario 1, we observed a significant outpouching of the posterior pole, closely resembling the shape of a Type-III staphyloma. Additionally, we found a notable change in scleral curvature and a thinning of the peripapillary sclera by 84%. In contrast, scenario 2 and 3 exhibited less drastic deformations, with stable posterior staphylomas after approximately 7 years. Our proposed framework suggests that local scleral weakening is sufficient to trigger staphyloma formation under a normal level of intraocular pressure. Our model also reproduced characteristics of Type-III staphylomas. With patient-specific scleral geometries (as could be obtained with wide-field optical coherence tomography), our framework could be clinically translated to help us identify those at risks of developing posterior staphylomas.
本研究旨在评估生长和重塑(G&R)理论是否可以解释巩膜葡萄肿的形成,这种葡萄肿可能是由于年龄相关的弹性蛋白降解、近视进展或其他因素导致的局部巩膜弱化引起的。重建了健康眼睛的有限元模型,包括小梁网、视盘周围巩膜和周边巩膜。采用均匀化约束混合模型模拟巩膜在其生物力学环境发生变化时的适应过程,时间跨度为 13.7 年。通过将视盘周围巩膜和小梁网的基质剪切刚度降低 85%,触发 G&R 过程。研究了三种不同的 G&R 情况:(1)低质量周转率与壁内体积生长相结合;(2)高质量周转率与壁内体积生长相结合;(3)高质量周转率与质量密度生长相结合。在情况 1 中,我们观察到后极明显的外膨,与 III 型巩膜葡萄肿的形状非常相似。此外,我们还发现巩膜曲率有明显变化,视盘周围巩膜厚度减少了 84%。相比之下,情况 2 和 3 表现出较小的变形,大约 7 年后稳定的后巩膜葡萄肿。我们提出的框架表明,在正常眼压下,局部巩膜弱化足以引发巩膜葡萄肿的形成。我们的模型还再现了 III 型巩膜葡萄肿的特征。通过使用宽场光学相干断层扫描获得患者特定的巩膜几何形状,我们的框架可以在临床上转化,以帮助我们识别那些有发生后巩膜葡萄肿风险的患者。