Evidence map›Paper›PMID 42542868›Full record

ArticleJournal of ophthalmology2026

Classification of Inherited Retinal Diseases Using Artificial Intelligence Models for Fundus Autofluorescence and Ultrawide Retinal Images.

Han Trinh, Muhammad Ibrahim, Jason Charng, Zahra Tajbakhsh, Fred K Chen, Ajmal Mian, Khyber Alam

Abstract read
In one paragraph

Article in Journal of ophthalmology, 2026. 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

7 authors.

Han TrinhDepartment of Optometry and Vision Sciences, School of Health and Clinical Sciences, The University of Western Australia, Crawley, Western Australia, Australia, uwa.edu.au.ORCID https://orcid.org/0009-0003-2107-0710
Muhammad IbrahimSchool of Physics, Maths and Computing, Computer Science and Software Engineering, The University of Western Australia, Nedlands, Western Australia, Australia, uwa.edu.au.ORCID https://orcid.org/0000-0002-5376-2477
Jason CharngDepartment of Optometry and Vision Sciences, School of Health and Clinical Sciences, The University of Western Australia, Crawley, Western Australia, Australia, uwa.edu.au.ORCID https://orcid.org/0000-0002-5778-6310
Zahra TajbakhshDepartment of Optometry and Vision Sciences, School of Health and Clinical Sciences, The University of Western Australia, Crawley, Western Australia, Australia, uwa.edu.au.ORCID https://orcid.org/0000-0002-5432-1016
Fred K ChenCentre for Ophthalmology and Visual Sciences (Incorporating Lions Eye Institute), The University of Western Australia, Nedlands, Western Australia, Australia, uwa.edu.au.ORCID https://orcid.org/0000-0003-2809-9930
Ajmal MianSchool of Physics, Maths and Computing, Computer Science and Software Engineering, The University of Western Australia, Nedlands, Western Australia, Australia, uwa.edu.au.ORCID https://orcid.org/0000-0002-5206-3842
Khyber AlamDepartment of Optometry and Vision Sciences, School of Health and Clinical Sciences, The University of Western Australia, Crawley, Western Australia, Australia, uwa.edu.au.ORCID https://orcid.org/0000-0001-7779-0467

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background/Objectives: Inherited retinal diseases (IRDs) are a leading cause of blindness in working-age adults. Although artificial intelligence (AI) shows potential for disease classification, progress is limited by small datasets, reliance on labelled data and limited integration of multiple imaging modalities. RETFound, a foundation model pretrained on over 900,000 fundus photographs, may address these limitations. While RETFound is based on the transformer architecture, convolutional neural networks (CNNs), such as ResNet and EfficientNet_B0, have also demonstrated strong performance in classifying retinal diseases. This study adapted RETFound and CNNs for analysing fundus autofluorescence (FAF) and pseudocolour ultra-widefield (UWF) images, establishing a framework to classify IRDs. Subjects/Methods: Deidentified FAF and UWF images were obtained from controls and patients with Best disease, rod-cone dystrophy, Stargardt disease and choroideremia. Images underwent preprocessing and were used to fine-tune RETFound. Model performance was compared with classical machine learning algorithms (logistic regression, support vector machine, gradient boosting and random forest) and deep learning architectures (ResNet18, ResNet50, vision transformer, EfficientNet_B0 and ConvNeXt-Tiny) pretrained on ImageNet. Results: The fine-tuned RETFound model achieved an accuracy of 0.815, with the best performance for rod-cone dystrophy (F1 = 0.820). RETFound outperformed classical machine learning models and a vision transformer pretrained on ImageNet. ResNet18 achieved a weighted F1 of 0.839 and demonstrated the best classification performance for Stargardt disease and choroideremia (F1 0.821 and 0.728, respectively). ResNet50 achieved a weighted F1 of 0.825 and demonstrated the best classification performance for normal retinas and Best disease (F1 0.945 and 0.616, respectively). ResNet architectures achieved the best performance overall. Conclusions: ResNet architectures and fine-tuned RETFound both demonstrated strong accuracy in classifying IRD classes, demonstrating potential for clinical application and deployment in eye care settings as tools for IRD diagnosis, triage and management.

Identifiers

PMID42542868
PMCPMC13428240

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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.