Evidence map›Paper›PMID 40996501›Full record

ArticleGraefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie2025

Spatial distribution of Intra-retinal Hyper-reflective foci and impact on progression in eyes with intermediate Age-related macular degeneration.

Aditya Verma, Muneeswar G Nittala, Jonathan L Haines, Margaret A Pericak-Vance, Dwight Stambolian, SriniVas R Sadda

Abstract read
In one paragraph

Article in Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

6 authors.

Aditya VermaDoheny Eye Institute, Pasadena, CA, USA.
Muneeswar G NittalaDoheny Eye Institute, Pasadena, CA, USA.
Jonathan L HainesCleveland Institute for Computational Biology, Department of Population & Quantitative Health Sciences, School of Medicine, Case Western Reserve University, Cleveland, OH, 44106, USA.
Margaret A Pericak-VanceJohn P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, FL, Florida, 33136, USA.
Dwight StambolianDepartment of Ophthalmology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, 19104, USA.
SriniVas R SaddaDoheny Eye Institute, Pasadena, CA, USA. ssadda@doheny.org.ORCID http://orcid.org/0000-0002-4939-3306

Funding

Genetic Epidemiology of Age-Related Macular Degeneration in the Older Order AmishR01EY023164 · NEI · UNIVERSITY OF PENNSYLVANIA · PI PERICAK-VANCE, MARGARET A., STAMBOLIAN, DWIGHT EDWARD · 2013 to 2017
$6.2M
Epidemiology of Biomarkers of AMD ProgressionR01EY030614 · NEI · DOHENY EYE INSTITUTE · PI Jonathan L Haines, Margaret A. Pericak-Vance · 2021 to 2026
$3.0M
NEI NIH HHS R01 EY023164NEI NIH HHS R01EY023164 and 1R01EY030614NEI NIH HHS R01 EY030614
6 · The paper itself

Abstract

aimTo analyze the longitudinal spatial distribution characteristics of intraretinal hyperreflective foci (IHRF) in eyes with intermediate age-related macular degeneration (iAMD).

methodsThe optical coherence tomography (OCT) data was collected from the Amish Eye Study, for all patients with evidence of iAMD and IHRF at baseline, who completed a 24 month (M24) follow up visit. Early Treatment Diabetic Retinopathy Study (ETDRS) rings were placed on the enface scans from all volume scans showing IHRF, and the frequency and the density of IHRF was measured in the central subfield (CSF; 1 mm circle), the 1-3 mm ring (parafoveal region) and the 3-6 mm ring (perifoveal region). The distance of all IHRF lesions from the foveal center was measured.

resultsForty-nine eyes (40 subjects) had iAMD and IHRF at baseline and M24. 23 eyes (46.9%) showed progression to late AMD. The frequency of IHRF was greatest in the parafoveal ring, although the density was highest in the CSF. IHRF number and density numerically increased in all regions at M24, though the increase was significant only in the perifoveal region. Although regression analysis did not show a relationship between baseline IHRF distribution and risk for progression to late AMD at 2 years, eyes that developed late AMD at M24 tended to show a more eccentric distribution of IHRF over time.

conclusionsIHRF do not distribute evenly across the macula in eyes with iAMD, with a higher density centrally, but greater frequency parafoveally. IHRF tend to distribute more peripherally over time, however, among eyes that progress to late AMD. These observations may provide new insights into the pathophysiology of these lesions.

Indexed as

Macula LuteaMacular DegenerationAgedAged, 80 and overDisease ProgressionFemaleHumansMaleMiddle AgedTomography, Optical CoherenceAge-related macular degenerationIntraretinal hyper-reflective fociOptical coherence tomography

Identifiers

PMID40996501
PMCPMC12886317

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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.