Feature pitched transformer model for automated diabetic retinopathy severity classification on fundus images
摘要
Diabetic retinopathy (DR) is a leading cause of visual impairment worldwide. Early and accurate classification of disease severity using retinal fundus images is critical for timely diagnosis and prevention of vision loss. Automated systems can assist clinicians by improving screening efficiency and reducing diagnostic variability.
ObjectiveThis study proposes a novel feature-pitched classification model (FPCM) for automated classification of diabetic retinopathy stages using color fundus images, aiming to improve accuracy through enhanced feature extraction and spatial attention mechanisms.
MethodsThe proposed FPCM model extracts texture, intensity, and structural features from fundus images by identifying high-information regions referred to as pitch points. These features are processed using a concentric transformer learning (CTL) mechanism, which applies spatial attention across nested regions to capture both local and global patterns. The model was evaluated using the Kaggle Diabetic Retinopathy dataset. Performance metrics included accuracy, precision, and sensitivity. Statistical reliability was assessed using bootstrap-based confidence interval analysis, and results were compared with existing methods such as ERCN, EffNet-SVM, HPLBO_DMN, FCSAM, CLAHE TH, and MSTNet.
ResultsThe proposed model achieved an accuracy of 95.19%, precision of 95.66%, and sensitivity of 95.29%. Bootstrap analysis confirmed the robustness and statistical reliability of the performance. Comparative evaluation demonstrated that FPCM provides competitive or superior results relative to existing approaches.
ConclusionThe proposed FPCM model effectively enhances diabetic retinopathy severity classification by integrating pitch-point–based feature extraction with concentric transformer learning. The model demonstrates high accuracy and robustness while focusing on clinically relevant regions, improving both interpretability and diagnostic reliability. These findings highlight the potential of FPCM for deployment in automated retinal screening systems, although further validation on diverse clinical datasets is recommended.