AI可精准评估眼病进展,但预测未来恶化仍不足。
Deep Learning for Retinal Degeneration Assessment: A Comprehensive Analysis of the MARIO Challenge
- 用OCT和临床数据训练AI模型,判断眼病是否恶化
- 模型在判断当前变化上媲美医生,但预测3个月后病情差
- 适合眼科医生和算法研究者参考,推动智能诊疗
MARIO挑战赛于2024年MICCAI会议举行,聚焦通过光学相干断层扫描(OCT)图像自动化检测与监测年龄相关性黄斑变性(AMD)。挑战赛设计用于评估算法对AMD中新生血管活动变化的检测能力,采用多模态数据集。主数据集来自法国布雷斯特,供参赛团队训练与测试模型,最终排名基于此数据集表现。辅助数据集来自阿尔及利亚,用于赛后评估模型在人群与设备差异下的泛化能力。挑战包含两项任务:一是判断连续两张2D OCT B-scan之间的病变演变;二是预测接受抗血管内皮生长因子(anti-VEGF)治疗患者未来三个月的疾病进展。共35支队伍参与,前12名进入决赛并展示方法。本文详述挑战结构、任务设置、数据特征及优胜方案,建立以OCT、红外成像和临床数据(如就诊次数、年龄、性别等)为基础的AMD监测基准。结果显示,人工智能在判断当前病变演变方面达到医师水平(任务1),但在预测未来变化方面仍不及临床判断(任务2)。
原文摘要 · Abstract (English)
The MARIO challenge, held at MICCAI 2024, focused on advancing the automated detection and monitoring of age-related macular degeneration (AMD) through the analysis of optical coherence tomography (OCT) images. Designed to evaluate algorithmic performance in detecting neovascular activity changes within AMD, the challenge incorporated unique multi-modal datasets. The primary dataset, sourced from Brest, France, was used by participating teams to train and test their models. The final ranking was determined based on performance on this dataset. An auxiliary dataset from Algeria was used post-challenge to evaluate population and device shifts from submitted solutions. Two tasks were involved in the MARIO challenge. The first one was the classification of evolution between two consecutive 2D OCT B-scans. The second one was the prediction of future AMD evolution over three months for patients undergoing anti-vascular endothelial growth factor (VEGF) therapy. Thirty-five teams participated, with the top 12 finalists presenting their methods. This paper outlines the challenge's structure, tasks, data characteristics, and winning methodologies, setting a benchmark for AMD monitoring using OCT, infrared imaging, and clinical data (such as the number of visits, age, gender, etc.). The results of this challenge indicate that artificial intelligence (AI) performs as well as a physician in measuring AMD progression (Task 1) but is not yet able of predicting future evolution (Task 2).
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