Evidence map›Paper›PMID 39578549›Full record

ReviewEye (London, England)2025

Photoreceptor assessment in age-related macular degeneration.

Amitha Domalpally, Anna-Maria Haas, Shruti Chandra, Brandon VanderZee, Ioannis S Dimopoulos, Tiarnan D L Keenan, Jeong W Pak, Karl G Csaky, Barbara A Blodi, Sobha Sivaprasad

Abstract readReview
In one paragraph

Review in Eye (London, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
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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

10 authors.

Amitha DomalpallyWisconsin Reading Center, Dept of Ophthalmology and Visual Sciences, University of Wisconsin, Madison, USA. domalpally@wisc.edu.ORCID 0000-0002-8145-9619
Anna-Maria HaasWisconsin Reading Center, Dept of Ophthalmology and Visual Sciences, University of Wisconsin, Madison, USA.
Shruti ChandraMoorfields Clinical Research Facility, NIHR Biomedical Research Centre, Moorfields Eye Hospital NHS Foundation Trust, London, UK.ORCID 0000-0002-2634-9775
Brandon VanderZeeWisconsin Reading Center, Dept of Ophthalmology and Visual Sciences, University of Wisconsin, Madison, USA.
Ioannis S DimopoulosNational Eye Institute, National Institutes of Health, Bethesda, MD, USA.
Tiarnan D L KeenanNational Eye Institute, National Institutes of Health, Bethesda, MD, USA.ORCID 0000-0002-2253-1772
Jeong W PakWisconsin Reading Center, Dept of Ophthalmology and Visual Sciences, University of Wisconsin, Madison, USA.
Karl G CsakyRetina Foundation of the Southwest, Dallas, TX, USA.
Barbara A BlodiWisconsin Reading Center, Dept of Ophthalmology and Visual Sciences, University of Wisconsin, Madison, USA.
Sobha SivaprasadMoorfields Clinical Research Facility, NIHR Biomedical Research Centre, Moorfields Eye Hospital NHS Foundation Trust, London, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Clinical trials investigating drugs for various stages of age-related macular degeneration (AMD) are actively underway and there is a strong interest in outcomes that demonstrate a structure-function-correlation. The ellipsoid zone (EZ), a crucial anatomical feature affected in this disease, has emerged as a strong contender. There is significant interest in evaluating EZ metrics on Optical Coherence Tomography (OCT), such as integrity and reflectivity, as disruption of this photoreceptor-rich layer may indicate disease progression. Loss of photoreceptor integrity in the junctional zone of geographic atrophy (GA) has been shown to exceed the areas of retinal pigment epithelial (RPE) atrophy, thus predicting future GA expansion. Furthermore, reduced visual acuity and retinal sensitivity have been correlated with loss of EZ integrity, underscoring a structure-function relationship. Photoreceptor integrity has also recently been acknowledged by the Food and Drug Administration (FDA), supporting its use as a primary endpoint in clinical trials investigating treatments for GA. However, the segmentation of this EZ still poses challenges. Continuous enhancements in OCT resolution and advancements in automated segmentation algorithms contribute to improved assessment of the EZ, strengthening its potential as an imaging biomarker for assessing photoreceptor function. It remains to be seen whether the EZ will serve as a surrogate marker for intermediate AMD. This article aims to provide an overview of the current understanding and knowledge of the EZ, while addressing ongoing challenges encountered in its assessment and interpretation.

Indexed as

Geographic AtrophyMacular DegenerationPhotoreceptor Cells, VertebrateTomography, Optical CoherenceHumansRetinal Pigment EpitheliumVisual Acuity

Identifiers

PMID39578549
PMCPMC11751396

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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 Socratic graph.