4.4 Article

RETINAL ANGIOMATOUS PROLIFERATION A Quantitative Analysis of the Fundoscopic Features of the Fellow Eye

Journal

RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES
Volume 35, Issue 10, Pages 1985-1991

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/IAE.0000000000000619

Keywords

age-related macular degeneration; choroidal neovascularization; neovascular phenotypes; retina; retinal neovascularization; retinal angiomatous proliferation; type 3 neovascularization

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Purpose:To quantitatively analyze and compare the fundoscopic features between fellow eyes of retinal angiomatous proliferation and typical exudative age-related macular degeneration and to identify possible predictors of neovascularization.Methods:Retrospective case-control study. Seventy-nine fellow eyes of unilateral retinal angiomatous proliferation (n = 40) and typical exudative age-related macular degeneration (n = 39) were included. Fundoscopic features of the fellow eyes were assessed using digital color fundus photographs taken at the time of diagnosis of neovascularization in the first affected eye. Grading was performed by two independent graders using RetmarkerAMD, a computer-assisted grading software based on the International Classification and Grading System for age-related macular degeneration.Results:Baseline total number and area (square micrometers) of drusen in the central 1,000, 3,000, and 6,000 m were considerably inferior in the fellow eyes of retinal angiomatous proliferation, with statistically significant differences (P < 0.05) observed in virtually every location (1,000, 3,000, and 6,000 m). A soft drusen (125 m) area >510,196 m(2) in the central 6,000 m was associated with an increased risk of neovascularization (hazard ratio, 4.35; 95% confidence interval [1.56-12.15]; P = 0.005).Conclusion:Baseline fundoscopic features of the fellow eye differ significantly between retinal angiomatous proliferation and typical exudative age-related macular degeneration. A large area (>510,196 m(2)) of soft drusen in the central 6,000 m confers a significantly higher risk of neovascularization and should be considered as a phenotypic risk factor.

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