Imaging biomarkers and artificial intelligence for diagnosis, prediction, and therapy of macular fibrosis in age-related macular degeneration: Narrative review and future directions.

IF 2.4 3区 医学 Q2 OPHTHALMOLOGY
Rishikesh Gandhewar, Thales Guimaraes, Sagnik Sen, Nikolas Pontikos, Ismail Moghul, Theodoros Empeslidis, Michel Michaelides, Konstantinos Balaskas
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引用次数: 0

Abstract

Macular fibrosis is an end-stage complication of neovascular Age-related Macular Degeneration (nAMD) with a complex and multifactorial pathophysiology that can lead to significant visual impairment. Despite the success of anti-vascular endothelium growth factors (anti-VEGF) over the last decade that revolutionised the management and visual prognosis of nAMD, macular fibrosis develops in a significant proportion of patients and, along with macular atrophy (MA), is a main driver of long-term vision deterioration. There remains an unmet need to better understand macular fibrosis and develop anti-fibrotic therapies. The use of imaging biomarkers in combination with novel Artificial Intelligence (AI) algorithms holds significant potential for improving the accuracy of diagnosis, disease monitoring, and therapeutic discovery for macular fibrosis. In this review, we aim to provide a comprehensive overview of the current state of knowledge regarding the various imaging modalities and biomarkers for macular fibrosis alongside outlining potential avenues for AI applications. We discuss manifestations of macular fibrosis and its precursors with diagnostic and prognostic significance on various imaging modalities, including Optical Coherence Tomography (OCT), Colour Fundus Photography (CFP), Fluorescein Angiography (FA), OCT-Angiography (OCTA) and collate data from prospective and retrospective research on known biomarkers. The predominant role of OCT for biomarker identification is highlighted. The review coincides with a resurgence of intense research interest in academia and industry for therapeutic discovery and clinical testing of anti-fibrotic molecules.

成像生物标志物和人工智能用于年龄相关性黄斑变性中黄斑纤维化的诊断、预测和治疗:叙述回顾和未来方向。
黄斑纤维化是新生血管性年龄相关性黄斑变性(nAMD)的终末期并发症,具有复杂的多因素病理生理,可导致严重的视力损害。尽管抗血管内皮生长因子(anti-VEGF)在过去十年中取得了成功,彻底改变了nAMD的治疗和视力预后,但黄斑纤维化在很大比例的患者中发展,并与黄斑萎缩(MA)一起,是长期视力恶化的主要驱动因素。更好地了解黄斑纤维化和开发抗纤维化疗法的需求仍未得到满足。将成像生物标志物与新型人工智能(AI)算法结合使用,在提高黄斑纤维化的诊断、疾病监测和治疗发现的准确性方面具有重大潜力。在这篇综述中,我们的目标是提供关于黄斑纤维化的各种成像方式和生物标志物的知识现状的全面概述,同时概述人工智能应用的潜在途径。我们讨论黄斑纤维化的表现及其前兆在各种成像方式上的诊断和预后意义,包括光学相干断层扫描(OCT)、彩色眼底摄影(CFP)、荧光素血管造影(FA)、OCT血管造影(OCTA),并整理来自已知生物标志物的前瞻性和回顾性研究数据。强调了OCT在生物标志物鉴定中的主要作用。这篇综述恰逢学术界和工业界对抗纤维化分子的治疗发现和临床试验的强烈研究兴趣的复苏。
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来源期刊
CiteScore
5.40
自引率
7.40%
发文量
398
审稿时长
3 months
期刊介绍: Graefe''s Archive for Clinical and Experimental Ophthalmology is a distinguished international journal that presents original clinical reports and clini-cally relevant experimental studies. Founded in 1854 by Albrecht von Graefe to serve as a source of useful clinical information and a stimulus for discussion, the journal has published articles by leading ophthalmologists and vision research scientists for more than a century. With peer review by an international Editorial Board and prompt English-language publication, Graefe''s Archive provides rapid dissemination of clinical and clinically related experimental information.
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