Photobiomodulation Therapy for Non-exudative Age-related Macular Degeneration.

Q3 Medicine
International Ophthalmology Clinics Pub Date : 2025-01-01 Epub Date: 2024-12-23 DOI:10.1097/IIO.0000000000000543
Daniel A Rodriguez, Alex Song, Anshul Bhatnagar, Christina Y Weng
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引用次数: 0

Abstract

Age-related macular degeneration (AMD) is a chronic condition that causes gradual central vision loss, most commonly in patients 50 years or older. This disease is commonly classified as either dry (non-exudative) or wet (exudative). Most patients with AMD have the non-exudative form, characterized by the presence of drusen in the macula. These patients can be further subclassified based on drusen size into early, intermediate, or late stages. The pathogenesis of this disease is quite complex and has been linked to genetic variations, dysfunction of normal retinal homeostasis, chronic inflammation, and mitochondrial dysfunction. Current treatment options for patients with intermediate dry AMD are limited to lifestyle modifications and vitamin supplementation. Photobiomodulation therapy (PBT) has been proposed as an additional therapy for this disease. Early animal and human studies have shown that PBT can alter many of the pathways implicated in the pathogenesis of AMD including improving mitochondrial function, decreasing inflammation, and promoting wound healing. Clinical trials investigating the use of PBT in patients with non-exudative AMD have shown promising results. Many of these trials showed improvement in both clinical (visual acuity and contrast sensitivity) as well as anatomic (drusen volume and area geographic atrophy) variables. Most, however, are limited by sample size, differences in treatment algorithm, and populations tested. Ongoing clinical trials aim to expand on this work with longer follow-up, larger sample sizes, and studying a global population. Further work is needed to determine ideal treatment algorithms and patient populations that may benefit the most from this technology.

非渗出性老年性黄斑变性的光生物调节治疗。
年龄相关性黄斑变性(AMD)是一种慢性疾病,可导致逐渐的中央视力丧失,最常见于50岁或以上的患者。这种疾病通常分为干性(非渗出性)和湿性(渗出性)两种。大多数黄斑变性患者为非渗出性黄斑变性,其特征是黄斑中存在脓样。这些患者可根据结节大小进一步细分为早期、中期或晚期。这种疾病的发病机制相当复杂,与遗传变异、正常视网膜稳态功能障碍、慢性炎症和线粒体功能障碍有关。目前对中度干性AMD患者的治疗选择仅限于改变生活方式和补充维生素。光生物调节疗法(PBT)已被提议作为该疾病的额外治疗。早期动物和人体研究表明,PBT可以改变与AMD发病机制有关的许多途径,包括改善线粒体功能、减少炎症和促进伤口愈合。研究PBT在非渗出性AMD患者中的应用的临床试验显示出令人鼓舞的结果。其中许多试验显示临床(视力和对比敏感度)和解剖(水肿体积和地理萎缩面积)变量均有改善。然而,大多数研究都受到样本量、治疗算法差异和测试人群的限制。正在进行的临床试验旨在通过更长时间的随访、更大的样本量和对全球人群的研究来扩展这项工作。需要进一步的工作来确定理想的治疗算法和可能从这项技术中获益最多的患者群体。
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来源期刊
International Ophthalmology Clinics
International Ophthalmology Clinics Medicine-Ophthalmology
CiteScore
1.40
自引率
0.00%
发文量
94
期刊介绍: International Ophthalmology Clinics is a valuable resource for any medical professional seeking to stay informed and up-to-date regarding developments in this dynamic specialty. Each issue of this quarterly publication presents a comprehensive review of a single topic in a new or changing area of ophthalmology. The timely, tightly focused review articles found in this publication give ophthalmologists the opportunity to benefit from the knowledge of leading experts in this rapidly changing field.
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