通过计算机试验推进视网膜疾病的治疗

IF 5 Q1 ENGINEERING, BIOMEDICAL Progress in biomedical engineering (Bristol, England) Pub Date : 2023-03-29 DOI:10.1088/2516-1091/acc8a9
R. Hernández, P. A. Roberts, W. El-Bouri
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引用次数: 2

摘要

治疗视网膜疾病以预防视力丧失是一项日益重要的挑战。由于眼睛的结构,视网膜可以相对容易地在原位检查。由于近年来扫描设备的技术发展,在了解视网膜结构和表征视网膜生物标志物方面取得了很大进展。然而,治疗选择仍然有限,而且往往效率和疗效都很低。近年来,许多制药公司采用了计算机临床试验(isct)的概念来优化和加速治疗方法的开发。isct依赖于使用基于支撑生物系统的物理和生化机制的数学模型。通过适当的简化和假设,人们可以生成各种治疗方案的计算机模拟,新的治疗分子,递送策略等等,快速而成本只是等效实验所需的一小部分。这种模拟不仅有可能加速治疗方法和策略的发展,而且有可能优化现有治疗方法的使用。在本文中,我们回顾了数学家、生物医学科学家和临床医生使用的最先进的视网膜计算机模型,强调了开发isct的挑战。在这篇论文中,我们强调了在健康和疾病中视网膜生理学的计算机模型的主要发现。我们描述了isct的主要组成部分,并确定了发展视网膜疾病isct的挑战。
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Advancing treatment of retinal disease through in silico trials
Treating retinal diseases to prevent sight loss is an increasingly important challenge. Thanks to the configuration of the eye, the retina can be examined relatively easily in situ. Owing to recent technological development in scanning devices, much progress has been made in understanding the structure of the retina and characterising retinal biomarkers. However, treatment options remain limited and are often of low efficiency and efficacy. In recent years, the concept of in silico clinical trials (ISCTs) has been adopted by many pharmaceutical companies to optimise and accelerate the development of therapeutics. ISCTs rely on the use of mathematical models based on the physical and biochemical mechanisms underpinning a biological system. With appropriate simplifications and assumptions, one can generate computer simulations of various treatment regimens, new therapeutic molecules, delivery strategies and so forth, rapidly and at a fraction of the cost required for the equivalent experiments. Such simulations have the potential not only to hasten the development of therapies and strategies but also to optimise the use of existing therapeutics. In this paper, we review the state-of-the-art in in silico models of the retina for mathematicians, biomedical scientists and clinicians, highlighting the challenges to developing ISCTs. Throughout this paper, we highlight key findings from in silico models about the physiology of the retina in health and disease. We describe the main building blocks of ISCTs and identify challenges to developing ISCTs of retinal diseases.
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