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Innovative technologies for the treatment of dry age-related macular degeneration (AMD) - modern therapeutic perspectives and their future

Review · human · Romanian journal of ophthalmology · 2025 · DOI 10.22336/rjo.2025.03 · PMID 40330967

Plain-language summary

Paraphrased from the published abstract below — not a verdict on whether anything works.

This review discusses current and emerging therapies for the dry form of age-related macular degeneration (AMD), covering AREDS/AREDS2 supplementation, molecularly targeted drugs, gene therapy, cell transplants, tissue engineering, nanotechnology, light-based therapies, and AI-based predictive modeling. The review describes AREDS/AREDS2 therapies as associated with slowing disease progression, though not reversing retinal damage. It also discusses molecularly targeted therapies (Pegcetacoplan, Avacincaptad Pegol) aimed at reducing inflammation, gene therapy (HMR59) aimed at protecting retinal pigment epithelium (RPE) cells, and mitochondria-targeted drugs (SS-31) aimed at mitigating oxidative stress, alongside scaffolds, nanoparticles, and light-based therapies (LLLT, adaptive phototherapy) described as supporting RPE regeneration and mitochondrial function. The authors state further clinical trials are needed.

Abstract

This review explores modern therapeutic options for the dry form of age-related macular degeneration (AMD), a condition representing one of the most significant challenges in ophthalmology due to its progressive nature and lack of effective treatment. The study discusses innovative approaches, evaluates available methods, and examines the potential of emerging technologies to improve patients' quality of life. A comprehensive review of current literature was conducted, being focused on therapies for dry AMD, including classical methods such as AREDS/AREDS2 supplementation, molecularly targeted drugs, gene therapy, cell transplants, tissue engineering, nanotechnology, and light-based therapies. Emerging tools leveraging artificial intelligence for personalized treatment and predictive modeling were also evaluated. AREDS/AREDS2 therapies effectively slow disease progression but cannot reverse retinal damage. Advances include molecularly targeted therapies (Pegcetacoplan, Avacincaptad Pegol) that reduce inflammation, gene therapy (HMR59) protecting RPE cells, and mitochondria-targeted drugs (SS-31) mitigating oxidative stress. Using scaffolds, nanoparticles, tissue engineering, and nanotechnology enhances RPE regeneration and drug delivery. Light-based therapies (LLLT, adaptive phototherapy) improve mitochondrial function, while AI aids in predicting disease progression and personalizing treatment. Modern therapeutic approaches for dry AMD provide promising avenues to slow disease progression and protect vision. However, further clinical trials are needed to optimize these strategies, assess long-term outcomes, and expand patient access to effective treatments. These advancements have the potential to significantly improve the quality of life for individuals affected by dry AMD.

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