Evidence map›Paper›PMID 34143819›Full record

ArticlePloS one2021

Quantifying frequency content in cross-sectional retinal scans of diabetics vs. controls.

Joel A Papay, Ann E Elsner

Open access · goldAbstract readComparative Study
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 42% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Cone Photoreceptors in Diabetic Patients.Frontiers in medicine · 2022
    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

2 authors at 1 institution in 1 country.

Joel A PapaySchool of Optometry, Indiana University, Bloomington, Indiana, United States of America.ORCID 0000-0002-9930-4754
Ann E ElsnerSchool of Optometry, Indiana University, Bloomington, Indiana, United States of America.ORCID 0000-0002-9040-9672
Indiana University Bloomington · US

Funding

SPATIAL EXTENT OF RETINAL DAMAGER01EY007624 · NEI · TRUSTEES OF INDIANA UNIVERSITY · PI ELSNER, ANN E · 1995 to 2012
$4.4M
Adaptive Optics Imaging of Human Retinal Vascular Structure and FunctionR01EY024315 · NEI · TRUSTEES OF INDIANA UNIVERSITY · PI BURNS, STEPHEN A · 2015 to 2024
$4.3M
System for Increasing Patient Access to Eye Exams for Diabetic RetinopathyR44EY020017 · NEI · AEON IMAGING, LLC · PI MULLER, MATTHEW S · 2009 to 2013
$3.2M
Core Support for Vision Research at Indiana UniversityP30EY019008 · NEI · TRUSTEES OF INDIANA UNIVERSITY · PI BURNS, STEPHEN A · 2009 to 2013
$2.1M
NEI NIH HHS P30 EY019008NEI NIH HHS R01 EY007624NEI NIH HHS R01 EY024315NEI NIH HHS R44 EY020017
6 · The paper itself

Abstract

purposeTo examine subtle differences in the structure of diabetic vs. control retinas.

methodsSpectral-domain optical coherence tomography (SD-OCT) images were compared for the retinas of 33 diabetic subjects who did not have clinical evidence of diabetic macular edema and age-matched controls, with central macular thicknesses of 275 and 276 microns, respectively. Cross-sectional retinal images through the fovea, called B-scans, were analyzed for spatial frequency content. The B-scans were processed to remove and smooth the portions of the retinal image not within regions of interest in the retina. The remaining retinal images were then quantified using a Fast Fourier Transform (FFT) approach that provided amplitude as a function of spatial frequency.

resultsThe FFT analysis showed that diabetic retinas had spatial frequency content with significantly higher power compared to control retinas particularly for a deeper fundus layer at mid-range spatial frequencies, ranging from p = 0.0030 to 0.0497 at 16.8 to 18.2 microns/cycle. There was lower power at higher spatial frequencies, ranging from p = 0.0296 and 0.0482 at 27.4 and 29.0 microns/cycle. The range of mid-range frequencies corresponds to the sizes of small blood vessel abnormalities and hard exudates. Retinal thickness did not differ between the two groups.

conclusionsDiabetic retinas, although not thicker than controls, had subtle but quantifiable pattern changes in SD-OCT images particularly in deeper fundus layers. The size range and distribution of this pattern in diabetic eyes were consistent with small blood vessel abnormalities and leakage of lipid and fluid. Feature-based biomarkers may augment retinal thickness criteria for management of diabetic eye complications, and may detect early changes.

Indexed as

Case-Control StudiesDiabetic RetinopathyDiagnosis, DifferentialFemaleHumansMacular EdemaMaleMiddle AgedRadiographic Image Interpretation, Computer-AssistedRetinaTomography, Optical Coherence

Identifiers

PMID34143819
PMCPMC8213050
OpenAlexW3172789891

What OpenQuestion holds

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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.