# Machine learning-based prediction of diabetic retinopathy from pupillary abnormalities in a South Indian population

**Authors:** Janani Surya, S Tamilselvi, Maitreyee Roy, Sivaraj Chinnasamy, Rajiv Raman, M Suchetha, Ganesh Rajendran, Tomo Popovic, Tomo Popovic, Tomo Popovic, Tomo Popovic

PMC · DOI: 10.1371/journal.pone.0340802 · PLOS One · 2026-01-22

## TL;DR

This study uses machine learning to predict diabetic retinopathy from pupillary changes in a South Indian population, showing promising accuracy.

## Contribution

The novel use of pupillary abnormalities as biomarkers for DR prediction using machine learning models, particularly ANN.

## Key findings

- ANN achieved an accuracy of 0.807 and AUC of 0.879 in predicting DR using pupillary parameters.
- Pupillary abnormalities were identified as effective biomarkers for DR risk detection.

## Abstract

Diabetic retinopathy (DR) is a common complication of diabetes that can lead to vision loss. Early detection and prevention of DR is crucial to reduce the burden of this disease. The purpose of this study was to build a prediction model for DR using pupillary abnormalities as biomarkers. Pupillary parameters including Dark-adapted Baseline Pupillary Diameter (BPD), Amplitude of Pupillary Constriction (APC), Velocity of Pupillary Constriction (VPC), Amplitude of Pupil Re-dilatation after Maximum Constriction, and Velocity of Pupillary Dilatation (VPD) were collected and analyzed using machine learning algorithm including Support Vector Machine, Decision Trees, Artificial Neural Networks (ANN), Logistic Regressions, Random Forest, Naive Bayes Classifier. Utilizing ROC analysis and the Youden index, this study identified cut-off values for pupillary abnormalities to detect DR risk. The study found that ANN performed well with an accuracy of 0.807 (95% CI: 0.65–0.94) and AUC of 0.879 (95% CI: 0.71–0.98) in predicting DR using pupillary abnormalities as biomarkers. The findings of this research offer significant insights into the predictive value of pupillary abnormalities for DR, establishing a strong foundation for early intervention strategies. Particularly, the superior performance of ANN in detecting DR presents an opportunity to refine risk stratification and prevention approaches, potentially transforming the prognosis for individuals at elevated risk of this condition.

## Linked entities

- **Diseases:** Diabetic retinopathy (MONDO:0005266), diabetes (MONDO:0005015)

## Full-text entities

- **Genes:** OPN4 (opsin 4) [NCBI Gene 94233] {aka MOP}
- **Diseases:** BPD (MESH:D015875), macular degeneration (MESH:D008268), retinopathy (MESH:D058437), hypertension (MESH:D006973), vision loss (MESH:D014786), proliferative diabetic retinopathy (OMIM:603933), neuro-optic dysfunction (MESH:C536203), type 2 diabetes (MESH:D003924), diabetic autonomic neuropathy (MESH:D003929), VPD (MESH:D002311), DR (MESH:D003930), glaucoma (MESH:D005901), Diabetes (MESH:D003920), neurological or ocular dysfunction (MESH:D009461), ocular or systemic disease (MESH:D034721), optic neuropathies (MESH:D009901), STR (MESH:D000033), Pupillary Abnormalities (MESH:D011681), blindness (MESH:D001766)
- **Chemicals:** PONE-D-25-25752R2 (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12826491/full.md

## References

33 references — full list in the complete paper: https://tomesphere.com/paper/PMC12826491/full.md

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Source: https://tomesphere.com/paper/PMC12826491