| Issue |
ITM Web Conf.
Volume 79, 2025
International Conference on Knowledge Engineering and Information Systems (KEIS-2025)
|
|
|---|---|---|
| Article Number | 01036 | |
| Number of page(s) | 8 | |
| DOI | https://doi.org/10.1051/itmconf/20257901036 | |
| Published online | 08 October 2025 | |
DR-MobiCB-Onto: A Modular Framework for Lesion-Level Diabetic Retinopathy Detection and Ontology-Driven Semantic Reasoning
Department of Computers Techniques Engineering, College of Technical Engineering, The Islamic University, Najaf, Iraq
* Corresponding author: ali.alkwzahy.iu@gmail.com
Diabetic Retinopathy (DR) is a visual impairment caused by long-term diabetes that damages the blood vessels in the retina. It is one of the main causes of blindness worldwide, and early detection is very important to prevent progression. Therefore, existing Convolutional Neural Network (CNN)-based models have improved lesion detection, but lack semantic interpretability. While ontology-driven systems enable structured reasoning, they depend on precise lesion-level inputs, and bridging these paradigms enhances diagnostic reliability. Existing DR models have limitations in lesion-level accuracy, vessel segmentation, and semantic interpretation. To address these limitations, this research proposes a unified framework, namely, DR-MobiCB-Onto model comprising a modular DR detection pipeline integrating MobileNetV3 and Convolutional Block Attention Module (CBAM), namely DR-MobiCB with domain-specific ontology-driven reasoning for efficient lesion detection and semantic interpretation. Preprocessing to enhance the image includes bilateral filtering, CLAHEU, and Z-score normalization. The Extended Adaptive Density-Based Spatial Clustering (EADBSC) method is used to segment the Thick Blood Vessels (TBVs) in the enhanced image, and finally, lesions were detected using DR-MobiCB with dilated convolutions. Evaluation was performed on the Messidor and IDRiR datasets, obtaining 97.4% and 96.8% accuracy and AUC scores of 0.987 and 0.981, respectively.
© The Authors, published by EDP Sciences, 2025
This is an Open Access article distributed under the terms of the Creative Commons Attribution License 4.0, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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