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arXiv 2610.14138eess.IVcs.CV

利用视网膜基础模型探索AMD严重程度的潜在结构

Exploring the Latent Structure of AMD Severity Using Retinal Foundation Models

Polytechnic of Turin(都灵理工大学);The University of Osaka(大阪大学)

Niccolò Fineschi, Jovana Panic, Atsushi Watanabe, Hideaki Hayashi, Kazuya Nishimura, Yuki Maeno, Samanta Rosati, Gabriella Balestra, Kohji Nishida, Hajime Nagahara

AI总结:

本研究以AMD为案例,用RET-CLIP模型分析其嵌入空间中AMD严重程度的表征结构,发现其为连续谱,且该结构影响下游分类性能,还明确了关联的视网膜表型,为疾病研究提供了新视角。

摘要:

视网膜基础模型在广泛的眼科任务中展现出强大性能,但人们对其学习到的嵌入中疾病相关信息的表征方式,以及该分布是否会影响下游预测性能的了解相对较少。本研究以年龄相关性黄斑变性(AMD)为案例,使用来自AREDS数据集的双侧眼底图像,对比非视网膜编码器,探究视网膜视觉-语言基础模型RET-CLIP的嵌入空间中疾病严重程度的表征方式。我们首先表征学习表征空间内AMD严重程度的分布,随后评估该结构对三种临床相关、粒度递增的任务形式分类性能的影响。最后,结合特征归因、统计表型关联和定性图像分析,分析最具影响力的潜在维度。结果显示,RET-CLIP将AMD严重程度表征为连续谱而非一组离散类别,健康阶段与晚期疾病阶段的分离比中间阶段更清晰。该结构体现在下游性能中:二元AMD检测的平衡准确率为0.844,晚期AMD检测为0.814,而六分类分级则降至0.446。此外,最具影响力的潜在维度与不同视网膜表型存在统计关联,包括玻璃膜疣积累、色素改变和晚期视网膜病变。这些发现表明,视网膜基础模型表征的结构会影响临床相关预测任务的难度,也证明了表征水平分析在理解疾病组织和提升可解释性方面的潜力。

英文摘要:

Retinal foundation models have demonstrated strong performance across a wide range of ophthalmic tasks, yet relatively little is known about how disease-related information is represented within their learned embeddings and whether this distribution influences downstream prediction performance. In this work, we use Age-related Macular Degeneration (AMD) as a case study to investigate how disease severity is represented within the embedding space of RET-CLIP, a retinal vision-language foundation model, using bilateral fundus images from the AREDS dataset, benchmarked against non-retinal encoders. We first characterize the distribution of AMD severity within the learned representation space and then evaluate how this structure influences classification performance across three clinically relevant task formulations of increasing granularity. Finally, we analyze the most influential latent dimensions combining feature attribution, statistical phenotype association, and qualitative image analyses. Our results show that RET-CLIP represents AMD severity as a continuous spectrum rather than a set of discrete categories, with healthy and advanced disease stages exhibiting clearer separation than intermediate ones. This organization was reflected in downstream performance, which decreased from a balanced accuracy of 0.844 and 0.814 for binary AMD and Late-AMD detection respectively to 0.446 for six-class grading. Furthermore, the most influential latent dimensions were statistically associated to distinct retinal phenotypes, including drusen accumulation, pigmentary alterations, and advanced retinal lesions. These findings suggest that the structure of retinal foundation-model representations influences the difficulty of clinically relevant prediction tasks and demonstrate the potential of representation-level analysis for understanding disease organization and improving interpretability.

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