基于环形血管特征实现可解释的眼底图像分类
Interpretable Fundus Image Classification via Ring-Based Retinal Vasculature Features

- 以视盘为中心构建环状血管结构,量化几何、颜色、氧合及熵等特征
- 在HRF数据集上达91.1%准确率,媲美大规模预训练模型
- 适合需要可解释性与小样本场景的医学图像分析应用
眼底照相广泛用于眼部疾病筛查与监测,但多数现代分类方法依赖深层隐变量表示,缺乏可解释性。本研究提出一种基于视盘为中心的环状血管结构表示的可解释眼底图像分类框架。该方法在同心环区域中量化血管几何、颜色外观、与氧合相关的血管特征以及血管-背景熵。这些生理学驱动的描述符来源于血管掩码、图像强度和光学密度测量,并在环间聚合以捕捉血管属性的空间变化。仅使用定量血管描述符,该方法在三个公开眼底数据集上均取得良好分类性能。在HRF数据集上,使用自动生成的血管掩码达到91.1%准确率,与RETFound(一个在大规模眼底图像上预训练的视觉变换器)在相同评估设置下表现相当。附加分析表明,预训练图像模型对成像相关空间线索(如眼底尺度、视网膜在视野中的位置)及非血管图像特征敏感。该框架可支持可解释性疾病分类、定量视网膜表型分析与视网膜生物标志物发现,且无需大量任务特定训练数据。
原文摘要 · Abstract (English)
Retinal fundus photography is widely used for screening and monitoring ocular diseases, but many modern classification pipelines rely on deep latent representations and provide limited interpretability. This study develops an interpretable fundus image classification framework based on a ring-structured representation of the retinal vasculature centered on the optic disc. The method quantifies vessel geometry, color appearance, oxygenation-related vascular appearance, and vessel--background entropy within concentric retinal regions. These physiologically motivated descriptors are derived from vessel masks, image intensities, and optical-density measurements and aggregated across rings to capture spatial variation in vascular properties. Using only quantitative vascular descriptors, the proposed method achieved strong classification performance across three public fundus datasets. On HRF, it achieved 91.1\% accuracy using automatically generated vessel masks, matching RETFound, a vision transformer pretrained on large-scale retinal fundus image data, under the same evaluation setting. Additional analyses suggest that pretrained image models are sensitive to acquisition-related spatial cues, including fundus scale and retinal position within the field of view, as well as broader non-vessel image characteristics. This framework may support interpretable disease classification, quantitative retinal phenotyping, and retinal biomarker discovery without requiring large task-specific training datasets.
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