Evidence map›Paper›PMID 33633139›Full record

ArticleScientific reports2021

Precise higher-order reflectivity and morphology models for early diagnosis of diabetic retinopathy using OCT images.

A Sharafeldeen, M Elsharkawy, F Khalifa, A Soliman, M Ghazal, M AlHalabi, M Yaghi, M Alrahmawy, S Elmougy, H S Sandhu and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
6.1field-weighted citation impact, top 3% 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

18 citing papers in PubMed, 53 citations in OpenAlex.

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  6. Multimodality Fusion Strategies in Eye Disease Diagnosis.Journal of imaging informatics in medicine · 2024
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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

11 authors at 3 institutions in 3 countries.

A Sharafeldeen *BioImaging Laboratory, Department of Bioengineering, University of Louisville, Louisville, KY, USA.
M Elsharkawy *BioImaging Laboratory, Department of Bioengineering, University of Louisville, Louisville, KY, USA.
F KhalifaBioImaging Laboratory, Department of Bioengineering, University of Louisville, Louisville, KY, USA.
A SolimanBioImaging Laboratory, Department of Bioengineering, University of Louisville, Louisville, KY, USA.
M GhazalElectrical and Computer Engineering Department, Abu Dhabi University, Abu Dhabi, UAE.
M AlHalabiElectrical and Computer Engineering Department, Abu Dhabi University, Abu Dhabi, UAE.
M YaghiElectrical and Computer Engineering Department, Abu Dhabi University, Abu Dhabi, UAE.
M AlrahmawyFaculty of Computers and Information, Mansoura University, Mansoura, Egypt.
S ElmougyFaculty of Computers and Information, Mansoura University, Mansoura, Egypt.
H S SandhuDepartment of Ophthalmology and Visual Sciences, University of Louisville, Louisville, USA.
A El-BazBioImaging Laboratory, Department of Bioengineering, University of Louisville, Louisville, KY, USA. aselba01@louisville.edu.
University of Louisville · USAbu Dhabi University · AEMansoura University · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study proposes a novel computer assisted diagnostic (CAD) system for early diagnosis of diabetic retinopathy (DR) using optical coherence tomography (OCT) B-scans. The CAD system is based on fusing novel OCT markers that describe both the morphology/anatomy and the reflectivity of retinal layers to improve DR diagnosis. This system separates retinal layers automatically using a segmentation approach based on an adaptive appearance and their prior shape information. High-order morphological and novel reflectivity markers are extracted from individual segmented layers. Namely, the morphological markers are layer thickness and tortuosity while the reflectivity markers are the 1st-order reflectivity of the layer in addition to local and global high-order reflectivity based on Markov-Gibbs random field (MGRF) and gray-level co-occurrence matrix (GLCM), respectively. The extracted image-derived markers are represented using cumulative distribution function (CDF) descriptors. The constructed CDFs are then described using their statistical measures, i.e., the 10th through 90th percentiles with a 10% increment. For individual layer classification, each extracted descriptor of a given layer is fed to a support vector machine (SVM) classifier with a linear kernel. The results of the four classifiers are then fused using a backpropagation neural network (BNN) to diagnose each retinal layer. For global subject diagnosis, classification outputs (probabilities) of the twelve layers are fused using another BNN to make the final diagnosis of the B-scan. This system is validated and tested on 130 patients, with two scans for both eyes (i.e. 260 OCT images), with a balanced number of normal and DR subjects using different validation metrics: 2-folds, 4-folds, 10-folds, and leave-one-subject-out (LOSO) cross-validation approaches. The performance of the proposed system was evaluated using sensitivity, specificity, F1-score, and accuracy metrics. The system's performance after the fusion of these different markers showed better performance compared with individual markers and other machine learning fusion methods. Namely, it achieved [Formula: see text], [Formula: see text], [Formula: see text], and [Formula: see text], respectively, using the LOSO cross-validation technique. The reported results, based on the integration of morphology and reflectivity markers and by using state-of-the-art machine learning classifications, demonstrate the ability of the proposed system to diagnose the DR early.

Indexed as

Diabetic RetinopathyEarly DiagnosisHumansImage Processing, Computer-AssistedMachine LearningNeural Networks, ComputerRetinaTomography, Optical Coherence

Identifiers

PMID33633139
PMCPMC7907116
OpenAlexW3132146525

What OpenQuestion holds

Textmetadata
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.