Evidence map›Paper›PMID 42621341›Full record

ArticleOphthalmology science2026

High-Resolution and Multimodal Structural Phenotyping of Intermediate and Advanced Non-Neovascular Age-Related Macular Degeneration.

Chiara M Eandi, Valerie C Snyder, Kate Grieve, Kiyoko Gocho, Celine Chaumette, D Castro-Farias, Nate Norberg, Grace Eddy, Thomas R Friberg, Andrew W Eller and 6 more

Abstract read
In one paragraph

Article in Ophthalmology science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors.

Chiara M EandiPARIS Group, Vision Institute and Quinze-Vingts National Ophthalmology Hospital, Paris, France.
Valerie C SnyderDepartment of Ophthalmology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Kate GrievePARIS Group, Vision Institute and Quinze-Vingts National Ophthalmology Hospital, Paris, France.
Kiyoko GochoPARIS Group, Vision Institute and Quinze-Vingts National Ophthalmology Hospital, Paris, France.
Celine ChaumettePARIS Group, Vision Institute and Quinze-Vingts National Ophthalmology Hospital, Paris, France.
D Castro-FariasPARIS Group, Vision Institute and Quinze-Vingts National Ophthalmology Hospital, Paris, France.
Nate NorbergPARIS Group, Vision Institute and Quinze-Vingts National Ophthalmology Hospital, Paris, France.
Grace EddyDepartment of Ophthalmology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Thomas R FribergDepartment of Ophthalmology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Andrew W EllerDepartment of Ophthalmology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Kunal K DansinganiDepartment of Ophthalmology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Joseph N MartelDepartment of Ophthalmology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Jay ChhablaniDepartment of Ophthalmology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
José-Alain SahelPARIS Group, Vision Institute and Quinze-Vingts National Ophthalmology Hospital, Paris, France.
Michel PaquesPARIS Group, Vision Institute and Quinze-Vingts National Ophthalmology Hospital, Paris, France.
Ethan A RossiDepartment of Ophthalmology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.

Funding

Virus Production and Manipulation of Protein/Gene Expression ModuleP30EY008098 · NEI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Ethan A Rossi · 1989 to 2026
$17.8M
Distinguishing normal aging from age-related macular degeneration at the level of single cells in the living human eyeR01EY030517 · NEI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI ROSSI, ETHAN A · 2020 to 2024
$2.4M
NEI NIH HHS P30 EY008098NEI NIH HHS R01 EY030517
6 · The paper itself

Abstract

Purpose: To characterize structural phenotypes in intermediate and advanced non-neovascular age-related macular degeneration (AMD) using flood-illumination adaptive optics (FIAO) and to explore their relationship with established multimodal imaging biomarkers, including OCT-based atrophy classifications. Design: Prospective, cross-sectional observational study. Subjects: A total of 208 eyes from 117 patients (mean age 74 years; 63% female) with intermediate AMD (iAMD) or geographic atrophy (GA) were enrolled. Eligible participants had visual acuity ≥20/63, refractive error between -6 and +2 diopters, and sufficient media clarity for high-quality imaging. Methods: Participants underwent multimodal imaging, including color fundus photography, spectral-domain OCT, infrared reflectance, fundus autofluorescence, and FIAO. Structural phenotypes (drusen, subretinal drusenoid deposits, pigmentary changes, and GA margins) were assessed qualitatively across modalities. Flood-illumination adaptive optics features were compared with OCT-based atrophy classifications (incomplete and complete retinal pigment epithelium and outer retinal atrophy [iRORA and cRORA]) using descriptive analyses and cross-tabulation. Main Outcome Measures: Prevalence and multimodal characteristics of AMD structural phenotypes, and their correspondence with FIAO features. Results: Drusen and pigmentary abnormalities were detected in the majority of eyes across modalities, with variability in prevalence depending on imaging technique. Flood-illumination adaptive optics identified drusen in 70% of eyes revealing a consistent reflectivity pattern of hyperreflective borders and hyporeflective centers. Hyporeflective clumps corresponding to pigmentary changes were always observed on FIAO, frequently localizing to areas of atrophy or transition zones. Distinct FIAO-defined GA border phenotypes were observed, including well-demarcated and indistinct margins. In descriptive cross-tabulation, well-demarcated FIAO borders were more frequently associated with OCT-defined cRORA, whereas indistinct or hyporeflective margins were with iRORA. Conclusions: Flood-illumination adaptive optics provides high-resolution visualization of structural features in iAMD and GA, revealing distinct patterns of drusen, pigmentary changes, and atrophic margins. While certain FIAO features show qualitative correspondence with OCT-defined atrophy stages, these relationships remain descriptive. Further quantitative and longitudinal studies are needed to determine their clinical relevance and role in disease characterization. Financial Disclosures: Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.

Indexed as

Adaptive opticsAge-related macular degenerationDrusenGeographic atrophyPigment

Identifiers

PMID42621341
PMCPMC13487613

What OpenQuestion holds

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Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.