Prognostic value of intermediate age-related macular degeneration phenotypes for geographic atrophy progression
- PMID: 32269061
- PMCID: PMC7848046
- DOI: 10.1136/bjophthalmol-2020-316004
Prognostic value of intermediate age-related macular degeneration phenotypes for geographic atrophy progression
Abstract
Background: To characterise early stages of geographic atrophy (GA) development in age-related macular degeneration (AMD) and to determine the prognostic value of structural precursor lesions in eyes with intermediate (i) AMD on the subsequent GA progression.
Methods: Structural precursor lesions for atrophic areas (lesion size at least 0.5 mm² in fundus autofluorescence images) were retrospectively identified based on multimodal imaging and evaluated for association with the subsequent GA enlargement rates (square-root transformed, sqrt). A linear mixed-effects model was used to account for the hierarchical nature of the data with a Tukey post hoc test to assess the impact of the local precursor on the subsequent GA progression rate.
Results: A total of 39 eyes with GA of 34 patients with a mean age of 74.4±6.7 (±SD) years were included in this study. Five precursor lesions (phenotypes 1-5) preceding GA development were identified: large, sub-retinal pigment epithelial drusen (n=19), reticular pseudodrusen (RPD, n=10), refractile deposits (n=4), pigment epithelial detachment (n=4) and vitelliform lesions (n=2). Precursor lesions exhibited a significant association with the subsequent (sqrt) GA progression rates (p=0.0018) with RPD (phenotype 2) being associated with the fastest GA enlargement (2.29±0.52 (±SE) mm/year.
Conclusions: The results indicate the prognostic relevance of iAMD phenotyping for subsequent GA progression highlighting the role of structural AMD features across different AMD stages.
Keywords: degeneration; imaging; macula; retina.
© Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.
Conflict of interest statement
Competing interests: Non-financial support from Heidelberg Engineering to ST, MP; from CenterVue to ST, MP and MF; from Optos to ST, SS-V and MF. Grant from German Research Foundation (PF 950/1-1 to MP and FL 658/4-1 and Fl658/4-2 to MF); grant from Katairo to SS-V; from Acucela, CenterVue to SS-V and FGH; from Zeiss, Optos, NightStar X and Bioeq/Formycon to FGH. Personal fees from Heidelberg Engineering, Bayer and Novartis to ST; from Bioeq/Formycon, Galimedix to SS-V; from Pixium Vision, Lin Bioscience, Oxurion, Stealth Therapeutics, Kodiak to FGH. Patent pending: US20140303013A1 from MF.
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