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重新审视老问题:调节的三维建模揭示了与年龄相关的生物力学变化如何导致老视功能障碍。

A new look at an old problem: 3D modeling of accommodation reveals how age-related biomechanical changes contribute to dysfunction in presbyopia.

机构信息

Department of Biomedical Engineering, University of Virginia, Charlottesville, VA, USA.

Department of Bioengineering, University of California San Diego, La Jolla, CA, USA.

出版信息

Biomech Model Mechanobiol. 2024 Feb;23(1):193-205. doi: 10.1007/s10237-023-01767-6. Epub 2023 Sep 21.

Abstract

Presbyopia is an age-related ocular disorder where accommodative ability declines so that an individual's focusing range is insufficient to provide visual clarity for near and distance vision tasks without corrective measures. With age, the eye exhibits changes in biomechanical properties of many components involved in accommodation, including the lens, sclera, and ciliary muscle. Changes occur at different rates, affecting accommodative biomechanics differently, but individual contributions to presbyopia are unknown. We used a finite element model (FEM) of the accommodative mechanism to simulate age-related changes in lens stiffness, scleral stiffness, and ciliary contraction to predict differences in accommodative function. The FEM predicts how ciliary muscle action leads to lens displacement by initializing a tensioned unaccommodated lens (Phase 0) then simulating ciliary muscle contraction in accommodation (Phase 1). Model inputs were calibrated to replicate experimentally measured lens and ciliary muscle in 30-year-old eyes. Predictions of accommodative lens deformation were verified with additional imaging studies. Model variations were created with altered lens component stiffnesses, scleral stiffness, or ciliary muscle section activations, representing fifteen-year incremental age-related changes. Model variations predict significant changes in accommodative function with age-related biomechanical property changes. Lens changes only significantly altered lens thickening with advanced age (46% decrease at 75 years old) while sclera changes produced progressive dysfunction with increasing age (23%, 36%, 49% decrease at 45, 60, and 75 years old). Ciliary muscle changes effected lens position modulation. Model predictions identified potential mechanisms of presbyopia that likely work in combination to reduce accommodative function and could indicate effectiveness of treatment strategies and their dependency on patient age or relative ocular mechanical properties.

摘要

老花眼是一种与年龄相关的眼部疾病,随着年龄的增长,调节能力下降,导致个体的聚焦范围不足以在不采取矫正措施的情况下提供近距和远距视觉任务的清晰视力。眼睛的许多参与调节的组成部分的生物力学特性都发生了变化,包括晶状体、巩膜和睫状肌。这些变化的发生速度不同,对调节生物力学的影响也不同,但个体对老花眼的贡献尚不清楚。我们使用调节机制的有限元模型(FEM)来模拟晶状体硬度、巩膜硬度和睫状肌收缩的年龄相关变化,以预测调节功能的差异。FEM 通过初始化拉紧的未调节晶状体(第 0 阶段),然后模拟调节时睫状肌的收缩(第 1 阶段)来预测睫状肌作用如何导致晶状体位移。模型输入被校准以复制 30 岁眼睛的实验测量的晶状体和睫状肌。通过额外的成像研究验证了调节晶状体变形的预测。通过改变晶状体组件硬度、巩膜硬度或睫状肌节激活来创建模型变体,代表 15 年的与年龄相关的生物力学特性变化。模型变体预测了随着年龄相关生物力学特性变化,调节功能会发生显著变化。晶状体变化仅在年龄较大时显著改变晶状体增厚(75 岁时减少 46%),而巩膜变化随着年龄的增长导致进行性功能障碍(45 岁时减少 23%、60 岁时减少 36%、75 岁时减少 49%)。睫状肌变化影响晶状体位置调节。模型预测确定了可能共同作用以降低调节功能的老花眼潜在机制,并且可能表明治疗策略的有效性及其对患者年龄或相对眼部机械特性的依赖性。

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