Demonstrates improved polyp segmentation in colonoscopy, suggesting a new predictive coding approach.
Polyp segmentation in colonoscopy remains clinically challenging because existing deep learning models operate as feedforward systems: features are extracted, attention weights are computed, and predictions are generated in a single irreversible pass with no opportunity for revision. We propose GRAFNet, a segmentation framework that introduces three biologically inspired computational mechanisms absent from medical image analysis: (1) learnable orientation filters with centre-surround normalisation that adapt to diagnostically relevant edge structures, (2) parallel retinal pathways with lateral inhibition for competitive feature suppression across scales, and (3) predictive coding with inference-time feedback, which iteratively refines predictions by reconciling high-level hypotheses with low-level observations. These mechanisms are integrated through a closed-loop architecture where cortical feedback generates top-down predictions, computes prediction errors, and updates feature representations during inference, enabling the network to dynamically re-examine ambiguous regions. Across five polyp segmentation benchmarks, GRAFNet achieves state-of-the-art performance (0.929 Dice on CVC-ClinicDB, 0.915 on Kvasir-SEG, and 0.946 on CVC-300), with substantial gains on flat lesions (+ 9.8% over the best competitor) and reduced misclassification of challenging anatomical structures such as haustral folds (− 4.8%). Beyond empirical improvements, the framework provides interpretable insights into how recurrent feedback and competitive interactions improve segmentation under ambiguity.
No takes yet. Share an insight, caveat, or question.
Fofanah et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: