Improve Retinal Artery/Vein Classification via Channel Couplin
This work improves automated diagnosis of conditions like diabetic retinopathy by enhancing retinal vessel classification, though it appears incremental as it builds on existing CNN methods.
The paper tackled the problem of automated retinal artery/vein classification by addressing the limitation of existing methods that treat vessel, artery, and vein segmentation as separate binary tasks, achieving state-of-the-art results on three public datasets (RITE, LES-AV, and HRF).
Retinal vessel segmentation plays a vital role in analyzing fundus images for the diagnosis of systemic and ocular diseases. Building on this, classifying segmented vessels into arteries and veins (A/V) further enables the extraction of clinically relevant features such as vessel width, diameter and tortuosity, which are essential for detecting conditions like diabetic and hypertensive retinopathy. However, manual segmentation and classification are time-consuming, costly and inconsistent. With the advancement of Convolutional Neural Networks, several automated methods have been proposed to address this challenge, but there are still some issues. For example, the existing methods all treat artery, vein and overall vessel segmentation as three separate binary tasks, neglecting the intrinsic coupling relationships between these anatomical structures. Considering artery and vein structures are subsets of the overall retinal vessel map and should naturally exhibit prediction consistency with it, we design a novel loss named Channel-Coupled Vessel Consistency Loss to enforce the coherence and consistency between vessel, artery and vein predictions, avoiding biasing the network toward three simple binary segmentation tasks. Moreover, we also introduce a regularization term named intra-image pixel-level contrastive loss to extract more discriminative feature-level fine-grained representations for accurate retinal A/V classification. SOTA results have been achieved across three public A/V classification datasets including RITE, LES-AV and HRF. Our code will be available upon acceptance.