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Regenerative Therapy by Suprachoroidal Cell Autograft in Dry Age-related Macular Degeneration: Preliminary In Vivo Report
Published on: February 12, 2018
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Dry Age-Related Macular Degeneration: Distribution of Visual Acuity and Progression Risk in a Large Registry
Theodore Leng1, Jason Schwartz2, David Nimke2
1Byers Eye Institute at Stanford, Stanford University School of Medicine, Palo Alto, CA, USA.
Ophthalmology and Therapy
|November 12, 2022
Summary
Geographic atrophy (GA) in dry age-related macular degeneration (dAMD) progresses faster in later stages, with lower visual acuity (VA) at baseline. Understanding dAMD progression is key for developing effective treatments.
Area of Science:
- Ophthalmology
- Retinal Diseases
- Age-Related Macular Degeneration
Background:
- Dry age-related macular degeneration (dAMD) progression to geographic atrophy (GA) is a critical factor in late-stage disease.
- Characterizing visual acuity (VA) distribution and progression risk is essential for developing targeted dAMD treatments.
Purpose of the Study:
- To characterize the distribution of visual acuity (VA) categories in patients with dry age-related macular degeneration (dAMD).
- To evaluate the risk of VA progression based on the stage of dAMD, including geographic atrophy (GA).
Main Methods:
- Retrospective observational study using the American Academy of Ophthalmology IRIS® Registry (2016-2019).
- Analysis of 593,277 patients with dAMD, tracking VA measurements and progression to GA or neovascular AMD.
- Utilized statistical models to describe VA distribution and progression probability by disease stage.
Main Results:
- At baseline, 64.4% had mild, 29.4% intermediate, and 6.2% GA disease. Most patients had VA ≥20/63, except for those with GA with subfoveal involvement (72.0% had VA <20/63).
- Lower VA correlated with more advanced dAMD stages at baseline. Annual progression probability to GA ranged from 0.4% (mild) to 5.5% (intermediate).
- Annual progression probability to neovascular AMD was 0.5% (mild) and 8.0% (intermediate).
Conclusions:
- Patients with advanced dAMD exhibit lower baseline VA and faster progression.
- Findings underscore the significant disease burden and trajectory of dAMD.
- This study identifies critical unmet needs and opportunities for therapeutic development in dAMD.
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