Deep learning-based diagnostic classification of multiple sclerosis using multicenter optical coherence tomography data

IF 2.7 2区 医学 Q1 OPHTHALMOLOGY
Experimental eye research Pub Date : 2026-05-01 Epub Date: 2026-02-10 DOI:10.1016/j.exer.2026.110916
Zahra Khodabandeh , Hossein Rabbani , Neda Shirani Bidabadi , Fereshteh Ashtari , David H. Steel , Jaume Bacardit , Anya Hurlbert , Raheleh Kafieh
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引用次数: 0

Abstract

Background

Multiple sclerosis (MS) is a chronic inflammatory disorder of the central nervous system, where timely and accurate diagnosis is essential for effective management. Optical coherence tomography (OCT) enables non-invasive evaluation of retinal changes that may serve as biomarkers for MS. Unlike other ophthalmologic diseases, raw cross-sectional OCT images in MS show subtle alterations often indistinguishable from healthy controls (HCs). Consequently, retinal layer thickness and boundary-derived surface features offer greater discriminatory power.

Methods

We investigated three categories of artificial intelligence (AI) models: (1) feature extraction with auto-encoder (AE) and shallow networks, (2) custom-designed deep networks, and (3) fine-tuned pre-trained networks. Retinal layer thickness and surface maps derived from OCT were analyzed to determine the most informative features, with channel-wise combination and mosaicing applied for feature integration. Model interpretability was assessed using occlusion sensitivity and Gradient-weighted Class Activation Mapping (Grad-CAM) visualizations. The dataset included 38 HC and 78 MS eyes obtained from independent public and local sources. Patient-wise partitioning was implemented to prevent data leakage.

Results

The proposed deep network using channel-wise combined thickness maps of retinal nerve fiber layer (RNFL), ganglion cell and inner plexiform layer (GCIPL), and inner nuclear layer (INL) layers achieved balanced accuracy of 97.3% (SD = 4.16; 95% CI: 92.3–100%), specificity of 97.3% (SD = 5.59; 95% CI: 92.6–100%), sensitivity of 97.4% (SD = 3.54; 95% CI: 92.6–100%), g-mean of 97.3% (SD = 4.18; 95% CI: 92.24-100%), F1-score of 98.0% (SD = 3.86; 95% CI: 92.6–100%), and an AUC of 0.96 (SD = 0.08; 95% CI: 0.95–1.00). Notably, the high performance observed in internal cross-validation was achieved when public and local datasets were combined. However, performance decreased substantially in cross-dataset evaluations, where models were trained on one dataset and tested on the other, indicating limited external generalizability, particularly when trained on public data and applied to local clinical data.

Conclusions

AI-based analysis of OCT-derived retinal layer features enables accurate and interpretable classification of MS, supporting its potential as a valuable clinical biomarker.

Abstract Image

基于深度学习的多中心光学相干断层成像数据多发性硬化症诊断分类。
背景:多发性硬化症(MS)是一种中枢神经系统的慢性炎症性疾病,及时准确的诊断对有效的治疗至关重要。光学相干断层扫描(OCT)可以对视网膜变化进行无创评估,这些变化可能作为MS的生物标志物。与其他眼科疾病不同,MS的原始横断面OCT图像显示出与健康对照(hc)难以区分的细微变化。因此,视网膜层厚度和边界派生的表面特征提供了更大的区分能力。方法:我们研究了三类人工智能(AI)模型:(1)基于自编码器(AE)和浅层网络的特征提取,(2)定制设计的深层网络,以及(3)微调预训练网络。通过分析OCT得到的视网膜层厚度和表面图来确定最具信息量的特征,并使用通道组合和马赛克进行特征集成。使用遮挡敏感性和梯度加权类激活映射(梯度- cam)可视化来评估模型的可解释性。数据集包括38只HC和78只MS眼睛,这些眼睛来自独立的公共和当地来源。实现了病人分区以防止数据泄漏。结果:采用视网膜神经纤维层(RNFL)、神经节细胞和内丛状层(GCIPL)和内核层(INL)层的通道联合厚度图构建的深度网络,平衡准确率为97.3% (SD = 4.16, 95% CI: 92.3-100%),特异性为97.3% (SD = 5.59, 95% CI: 92.6-100%),灵敏度为97.4% (SD = 3.54, 95% CI: 92.6-100%), g均值为97.3% (SD = 4.18, 95% CI: 92.24-100%), f1评分为98.0% (SD = 3.86;95% CI: 92.6-100%), AUC为0.96 (SD = 0.08; 95% CI: 0.95-1.00)。值得注意的是,当公共数据集和本地数据集相结合时,在内部交叉验证中观察到的高性能得到了实现。然而,在跨数据集评估中,性能大幅下降,其中模型在一个数据集上训练并在另一个数据集上测试,这表明有限的外部泛化性,特别是在公共数据上训练并应用于本地临床数据时。结论:基于人工智能的oct衍生视网膜层特征分析能够准确和可解释地对MS进行分类,支持其作为有价值的临床生物标志物的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Experimental eye research
Experimental eye research 医学-眼科学
CiteScore
6.80
自引率
5.90%
发文量
323
审稿时长
66 days
期刊介绍: The primary goal of Experimental Eye Research is to publish original research papers on all aspects of experimental biology of the eye and ocular tissues that seek to define the mechanisms of normal function and/or disease. Studies of ocular tissues that encompass the disciplines of cell biology, developmental biology, genetics, molecular biology, physiology, biochemistry, biophysics, immunology or microbiology are most welcomed. Manuscripts that are purely clinical or in a surgical area of ophthalmology are not appropriate for submission to Experimental Eye Research and if received will be returned without review.
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