arXiv:2511.05106cs.CVcs.LG2025-11被引 1

用眼底OCT图像早期预测阿尔茨海默病,首次尝试直接分析原始影像。

Early Alzheimer's Disease Detection from Retinal OCT Images: A UK Biobank Study

论文配图:Early Alzheimer's Disease Detection from Retinal OCT Images: A UK Biobank Study
图 1 · 摘自论文原文
  • 直接用原始OCT图像做深度学习分类,跳过传统分割步骤。
  • 在4年预警期内达到AUC 0.62,虽未达临床标准但发现关键结构差异。
  • 适合关注眼科生物标志物与神经退行性疾病交叉研究的学者。

视网膜层厚度变化可通过光学相干断层扫描(OCT)测量,并与阿尔茨海默病(AD)等神经退行性疾病相关。以往研究多依赖分层厚度的定量分析,本研究首次探索直接对OCT B-scan图像进行分类以实现AD早期检测。不同于常规诊断任务,早期检测更具挑战性,因影像采集时间远早于临床确诊。我们基于英国生物银行队列,采用年龄、性别和成像次数匹配的受试者数据集,对多个预训练模型(包括ImageNet模型与OCT专用RETFound Transformer)进行微调与评估。针对小样本高维数据特点,结合标准与OCT特异性增强技术,并引入年份加权损失函数,优先关注影像后四年内确诊的病例。结果显示,ResNet-34表现最稳定,在4年队列中获得AUC 0.62。尽管未达临床应用阈值,可解释性分析揭示了中央黄斑区亚区在AD组与对照组间的结构差异。该研究为基于OCT的AD预测提供了基准,凸显了在临床确诊前数年捕捉细微视网膜生物标志物的难度,强调未来需更大规模数据集与多模态融合方法。

原文摘要 · Abstract (English)

Alterations in retinal layer thickness, measurable using Optical Coherence Tomography (OCT), have been associated with neurodegenerative diseases such as Alzheimer's disease (AD). While previous studies have mainly focused on segmented layer thickness measurements, this study explored the direct classification of OCT B-scan images for the early detection of AD. To our knowledge, this is the first application of deep learning to raw OCT B-scans for AD prediction in the literature. Unlike conventional medical image classification tasks, early detection is more challenging than diagnosis because imaging precedes clinical diagnosis by several years. We fine-tuned and evaluated multiple pretrained models, including ImageNet-based networks and the OCT-specific RETFound transformer, using subject-level cross-validation datasets matched for age, sex, and imaging instances from the UK Biobank cohort. To reduce overfitting in this small, high-dimensional dataset, both standard and OCT-specific augmentation techniques were applied, along with a year-weighted loss function that prioritized cases diagnosed within four years of imaging. ResNet-34 produced the most stable results, achieving an AUC of 0.62 in the 4-year cohort. Although below the threshold for clinical application, our explainability analyses confirmed localized structural differences in the central macular subfield between the AD and control groups. These findings provide a baseline for OCT-based AD prediction, highlight the challenges of detecting subtle retinal biomarkers years before AD diagnosis, and point to the need for larger datasets and multimodal approaches.

阿尔茨海默病OCT图像早期检测深度学习

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