Evidence map›Paper›PMID 41230898›Full record

ArticleTranslational vision science & technology2025

Perimetric Stimuli Undergoing Complete Spatial Summation Optimize the Detection of Retinal Ganglion Cell Density Gradients in Healthy Observers.

Caitlín S Campbell, Victoria Stapley, Roger S Anderson, David F Garway-Heath, Tony Redmond, Pádraig J Mulholland

Abstract read
In one paragraph

Article in Translational vision science & technology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

6 authors.

Caitlín S CampbellCentre for Optometry & Vision Science, Biomedical Sciences Research Institute, Ulster University, Coleraine, Northern Ireland, UK.
Victoria StapleyCentre for Optometry & Vision Science, Biomedical Sciences Research Institute, Ulster University, Coleraine, Northern Ireland, UK.
Roger S AndersonCentre for Optometry & Vision Science, Biomedical Sciences Research Institute, Ulster University, Coleraine, Northern Ireland, UK.
David F Garway-HeathNational Institute for Health & Care Research (NIHR) Biomedical Research Centre at Moorfields Eye Hospital NHS Foundation Trust and UCL Institute of Ophthalmology, London, UK.
Tony RedmondSchool of Optometry and Vision Sciences, Cardiff University, Cardiff, UK.
Pádraig J MulhollandCentre for Optometry & Vision Science, Biomedical Sciences Research Institute, Ulster University, Coleraine, Northern Ireland, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: To compare the ability of conventional luminance-modulating perimetric stimuli and an area-modulation stimulus (AMS) designed to measure changes in complete spatial summation to identify physiological retinal ganglion cell density (RGCD) gradients in healthy observers. Methods: Contrast thresholds were measured for Goldmann III (GIII; 0.43°, 200 ms) and V (GV; 1.72°, 200 ms) stimuli at 3° and 10° eccentricity in 100 healthy observers (median age, 43 years, range, 18-85 years), with mean spherical equivalent refractive errors ranging from -10.38 to +4.63 DS. Area thresholds were measured at the same locations using a fixed luminance stimulus (ΔL: 4.4 cd/m2, 200 ms). Colocalized RGCD estimates were determined using (i) optical coherence tomography (OCT) RGC layer thickness measures, and (ii) achromatic peripheral grating resolution acuity (PGRA) thresholds. Ratios of the difference in log energy threshold (ΔE) and log RGCD (ΔRGCD) between eccentricities were calculated (ΔE/|ΔRGCD|), with a value of 1 assumed to be the optimal relationship between functional thresholds and RGCD. Results: ΔE/|ΔRGCD|) values (median and interquartile range [IQR]) were largest for AMS (OCT, 0.54 [IQR, 0.37-0.78]; PGRA, 0.71 [IQR, 0.46-1.19]), followed by GIII (OCT, 0.29 [IQR, 0.08-0.44]; PGRA, 0.33 [IQR, 0.07-0.54]; and GV (OCT, 0.16 [IQR, 0.02-0.29]; and PGRA, 0.19 [IQR, 0.02-0.44]). Interstimulus differences between all stimulus pairs were statistically significant (AMS vs GIII, both P < 0.001; AMS vs GV, both P < 0.001; GIII vs GV, both P < 0.05). Conclusions: ΔE/|ΔRGCD| values were closest to 1 for AMS, suggesting this stimulus relates best to underlying physiological variations in RGCD. Translational Relevance: Thresholds measured with area modulation stimuli vary more proportionally with physiological changes in retinal ganglion cell density relative to conventional perimetric stimuli.

Indexed as

Retinal Ganglion CellsVisual FieldsVisual Field TestsAdolescentAdultAgedAged, 80 and overCell CountContrast SensitivityFemaleHumansMaleMiddle AgedPhotic StimulationSensory ThresholdsTomography, Optical Coherence

Identifiers

PMID41230898
PMCPMC12617668

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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.