Biomarker-Guided Management in Vitreoretinal Diseases: Integrating Imaging, Pharmacotherapy, and Surgical Decision-Making-A Narrative Review.

IF 2.1 2区 医学 Q2 OPHTHALMOLOGY
Matias Iglicki, Dinah Zur, Javier Ignacio Melamud, Anat Loewenstein
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引用次数: 0

Abstract

Purpose: To synthesize current evidence on imaging biomarkers in vitreoretinal diseases and to review the potential for a biomarker-guided framework integrating imaging, pharmacotherapy, and surgical decision-making in contemporary clinical practice.

Methods: This narrative review integrates published evidence and clinical insights on optical coherence tomography (OCT) and OCT angiography (OCTA)-derived biomarkers, focusing on their role in predicting disease behavior, therapeutic response, and surgical indications.

Results: Key imaging biomarkers-including disorganization of the retinal inner layers (DRIL), hyperreflective foci (HRF), intraretinal and subretinal fluid patterns, and vascular perfusion changes-demonstrate significant value in stratifying disease phenotype and guiding management. Biomarker-based approaches enable differentiation between angiogenic and inflammatory patterns, supporting individualized therapeutic strategies. These include optimized use of anti-vascular endothelial growth factor therapy, corticosteroid-based treatments, and newer long-acting agents. In addition, imaging biomarkers play a central role in identifying surgical candidates and determining timing of intervention, particularly in tractional maculopathies and refractory disease.

Conclusion: A biomarker-guided approach provides a clinically actionable framework for personalized vitreoretinal care. The integration of multimodal imaging with pharmacologic and surgical decision-making represents a critical step toward precision medicine, with the potential to improve outcomes and reduce treatment burden.

生物标志物引导的玻璃体视网膜疾病管理:整合成像、药物治疗和手术决策——一篇叙述性综述。
目的:综合目前关于玻璃体视网膜疾病成像生物标志物的证据,并回顾生物标志物指导框架在当代临床实践中整合成像、药物治疗和手术决策的潜力。方法:这篇叙述性综述整合了光学相干断层扫描(OCT)和OCT血管造影(OCTA)衍生生物标志物的已发表证据和临床见解,重点关注它们在预测疾病行为、治疗反应和手术指征方面的作用。结果:关键的成像生物标志物,包括视网膜内层紊乱(DRIL)、高反射灶(HRF)、视网膜内和视网膜下液体模式以及血管灌注改变,在疾病表型分层和指导治疗方面具有重要价值。基于生物标志物的方法能够区分血管生成和炎症模式,支持个性化治疗策略。这些包括优化使用抗血管内皮生长因子治疗,皮质类固醇为基础的治疗,和新的长效药物。此外,成像生物标志物在确定手术候选人和确定干预时机方面发挥着核心作用,特别是在牵引性黄斑病变和难治性疾病中。结论:生物标志物引导的方法为个性化玻璃体视网膜护理提供了临床可操作的框架。多模态成像与药理学和手术决策的整合是迈向精准医学的关键一步,具有改善结果和减轻治疗负担的潜力。
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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来源期刊
CiteScore
5.70
自引率
9.10%
发文量
554
审稿时长
3-6 weeks
期刊介绍: ​RETINA® focuses exclusively on the growing specialty of vitreoretinal disorders. The Journal provides current information on diagnostic and therapeutic techniques. Its highly specialized and informative, peer-reviewed articles are easily applicable to clinical practice. In addition to regular reports from clinical and basic science investigators, RETINA® publishes special features including periodic review articles on pertinent topics, special articles dealing with surgical and other therapeutic techniques, and abstract cards. Issues are abundantly illustrated in vivid full color. Published 12 times per year, RETINA® is truly a “must have” publication for anyone connected to this field.
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