Evidence map›Paper›PMID 40932447›Full record

ArticleTranslational vision science & technology2025

Code-Free Machine Learning for the Detection of Common Ophthalmic Diseases.

Trevor Lin, Theodore Leng

Abstract read
In one paragraph

Article in Translational vision science & technology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Trevor LinMorsani College of Medicine, University of South Florida, Tampa, FL, USA.
Theodore LengByers Eye Institute at Stanford, Stanford University School of Medicine, Palo Alto, CA, USA.

Funding

Stanford Vision Research CoreP30EY026877 · NEI · STANFORD UNIVERSITY · PI Jeffrey L Goldberg · 2017 to 2026
$8.0M
NEI NIH HHS P30 EY026877
6 · The paper itself

Abstract

Purpose: We explore a code-free method enabling physicians without programming experience to develop machine learning (ML) models for detecting diabetic retinopathy (DR), age-related macular degeneration (AMD), and glaucoma from fundus photographs. Methods: Two classification models were developed using Google Vertex AI's no-code AutoML Vision platform: a binary model detecting any pathology and a multi-class model classifying specific diseases. The development dataset consisted of 800 fundus photography images (200 each of DR, AMD, glaucoma, and normal) from the publicly available Fundus Image dataset for Vessel Segmentation. Ten percent of the dataset was saved for testing and 10% for internal validation. External validation was performed using the Eye Disease Diagnosis and Fundus Synthesis dataset, from which 100 single-diagnosis images per class were randomly selected (total N = 400). Model performances were evaluated using area under the precision-recall curve (AUPRC), precision, recall, accuracy, F1 score, and confidence score analysis. Results: Internally, the binary model yielded an AUPRC of 0.967, with 95.0% precision and recall. The multi-class model had an AUPRC of 0.906, with 91.0% precision and 90.0% recall. On external validation, the binary model reached 92.3% accuracy, whereas the multi-class model achieved 90% overall accuracy. Conclusions: Code-free ML approaches can enable physicians to create ML models for retinal disease detection without requiring programming expertise, supporting early detection of eye diseases. Translational Relevance: This work bridges the gap between AI research and clinical deployment by demonstrating that physicians can independently build ML models using accessible, no-code tools.

Indexed as

Diabetic RetinopathyEye DiseasesGlaucomaMachine LearningMacular DegenerationFundus OculiHumansPhotography

Identifiers

PMID40932447
PMCPMC12439502

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.