Evidence map›Paper›PMID 38010697›Full record

ArticleInvestigative ophthalmology & visual science2023

Spatial Summation in the Glaucomatous Macula: A Link With Retinal Ganglion Cell Damage.

Giovanni Montesano, Tony Redmond, Pádraig J Mulholland, David F Garway-Heath, Giovanni Ometto, Dario Romano, Federica Antonacci, Lucia Tanga, Carmela Carnevale, Luca M Rossetti and 2 more

Open access · goldAbstract read
In one paragraph

Article in Investigative ophthalmology & visual science, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 26% of its field
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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Trial
  2. 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

12 authors at 5 institutions in 2 countries.

Giovanni MontesanoCity, University of London, Optometry and Visual Sciences, London, United Kingdom.
Tony RedmondSchool of Optometry and Vision Sciences, Cardiff University, Cardiff, United Kingdom.
Pádraig J MulhollandNIHR Biomedical Research Centre, Moorfields Eye Hospital NHS Foundation Trust and UCL Institute of Ophthalmology, London, United Kingdom.
David F Garway-HeathNIHR Biomedical Research Centre, Moorfields Eye Hospital NHS Foundation Trust and UCL Institute of Ophthalmology, London, United Kingdom.
Giovanni OmettoCity, University of London, Optometry and Visual Sciences, London, United Kingdom.
Dario RomanoASST Santi Paolo e Carlo, Eye Clinic - University of Milan, Milan, Italy.
Federica AntonacciASST Santi Paolo e Carlo, Eye Clinic - University of Milan, Milan, Italy.
Lucia TangaIRCCS Fondazione Bietti, Rome, Italy.
Carmela CarnevaleIRCCS Fondazione Bietti, Rome, Italy.
Luca M RossettiASST Santi Paolo e Carlo, Eye Clinic - University of Milan, Milan, Italy.
David P CrabbCity, University of London, Optometry and Visual Sciences, London, United Kingdom.
Francesco OddoneIRCCS Fondazione Bietti, Rome, Italy.
Fondazione G.B. Bietti · ITMoorfields Eye Hospital NHS Foundation Trust · GBUniversity of Milan · ITCity, University of London · GBCardiff University · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: The purpose of this study was to test whether functional loss in the glaucomatous macula is characterized by an enlargement of Ricco's area (RA) through the application of a computational model linking retinal ganglion cell (RGC) damage to perimetric sensitivity. Methods: One eye from each of 29 visually healthy subjects <40 years old, 30 patients with glaucoma, and 20 age-similar controls was tested with a 10-2 grid with stimuli of 5 different area sizes. Structural estimates of point-wise RGC density were obtained from optical coherence tomography (OCT) scans. Structural and functional data from the young healthy cohort were used to estimate the parameters of a computational spatial summation model to generate a template. The template was fitted with a Bayesian hierarchical model to estimate the latent RGC density in patients with glaucoma and age-matched controls. We tested two alternative hypotheses: fitting the data by translating the template horizontally (H1: change in RA) or vertically (H2: loss of sensitivity without a change in RA). Root mean squared error (RMSE) of the model fits to perimetric sensitivity were compared. Ninety-five percent confidence intervals were bootstrapped. The dynamic range of the functional and structural RGC density estimates was denoted by their 1st and 99th percentiles. Results: The RMSE was 2.09 (95% CI = 1.92-2.26) under H1 and 2.49 (95% CI = 2.24-2.72) under H2 (P < 0.001). The average dynamic range for the structural RGC density estimates was only 11% that of the functional estimates. Conclusions: Macular sensitivity loss in glaucoma is better described by a model in which RA changes with RGC loss. Structural measurements have limited dynamic range.

Indexed as

GlaucomaRetinal Ganglion CellsAdultBayes TheoremHumansMacular DegenerationTomography, Optical CoherenceVisual FieldsVisual Field Tests

Identifiers

PMID38010697
PMCPMC10683773
OpenAlexW4389057909

What OpenQuestion holds

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LicenceCC BY
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 OpenQuestion graph.