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Integrating Retinal Segmentation Metrics with Machine Learning for Predictions from Mouse SD-OCT Scans.
Maide Gözde İnam1, Onur İnam1,2, Xiangjun Yang1
1Department of Ophthalmology, Edward S. Harkness Eye Institute, Columbia University, Vagelos College of Physicians and Surgeons, New York, NY, USA.
Current Eye Research
|January 23, 2025
Summary
Machine learning accurately predicts mouse age and species using retinal segmentation metrics from OCT scans. This approach offers a powerful tool for analyzing experimental models and predicting complex outcomes.
Area of Science:
- Ophthalmology
- Biomedical Engineering
- Machine Learning in Biology
Background:
- Optical Coherence Tomography (OCT) is crucial for non-invasive retinal imaging.
- Retinal layer thickness metrics can serve as biomarkers for biological variations.
- Machine learning (ML) offers advanced analytical capabilities for complex biological data.
Purpose of the Study:
- To evaluate the efficacy of ML algorithms in predicting biological features (mouse age and species) from retinal segmentation metrics.
- To determine if ML can categorize mice based on retinal structural data derived from OCT scans.
Main Methods:
- Retinal layer thickness data from C57BL/6 and DBA/2J mice were segmented from SD-OCT scans.
- Twenty-two ML models were trained to predict mouse groups (species and age).
- A neural network model was optimized, and performance metrics (accuracy, AUC, sensitivity, specificity, precision, F-1 score) were evaluated.
Main Results:
- Neural networks demonstrated significantly higher validation accuracy compared to other ML classifiers (p=0.005).
- The optimized neural network achieved 92.31% accuracy for species classification (C57BL/6 vs. DBA/2J) with an AUC of 0.9762.
- The model also achieved 82.05% accuracy for age group differentiation with an AUC of 0.9064.
Conclusions:
- ML analysis of retinal segmentation metrics from OCT scans is effective for categorical predictions in mouse models.
- This method provides a valuable, non-invasive approach for experimental research.
- Future expansion with histopathological and functional data may enhance predictive power for complex clinical and experimental outcomes.

