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arXiv Machine Learning · 2026/7/28 04:00:00

Dementia Etiology Diagnosis via Collaborative Meta Knowledge Enhancement

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痴呆症诊断一直是医学难题,不同病因的症状常常重叠,AI也难以准确区分。更麻烦的是,不同医院的检查数据存在差异,比如设备型号不同、检查项目不一样,这些“数据水土不服”会影响AI的表现。现在,研究人员提出了一个名为COME的新框架,核心思路是给AI加上“元信息感应器”——让AI在分析大脑影像时,自动识别这是哪家医院的设备、用了哪种检查方法,从而灵活适应不同数据来源。同时,团队还设计了一种“信任区域”训练机制,防止AI被数据中的偶然巧合误导。测试结果显示,COME在七个独立数据集中表现优异,平均准确率高达85.62%,比现有最强方法提升了4.29个百分点,而且跨医院、跨检查序列的泛化能力也很出色。这一技术的实际意义在于:未来患者在不同医院就诊时,AI都能给出稳定可靠的诊断建议;医生也能更早、更精准地识别痴呆类型(如阿尔茨海默病),从而制定个性化治疗方案。此外,AI的预测结果与患者的生物标志物(如淀粉样蛋白、tau蛋白)及临床严重程度高度吻合,这意味着诊断过程更加透明可解释,有助于建立医患信任。随着这种可扩展、可迁移的AI诊断系统逐步落地,痴呆症的早期筛查和精准医疗将迎来重要突破。
arXiv:2607.22770v1 Announce Type: new Abstract: Although artificial intelligence (AI) has shown promising performance in several medical tasks, accurate dementia etiology diagnosis with AI remains challenging due to complex overlapping symptoms among diseases. Scaling up the dataset size by combining the cross-center samples may bring a gain in the pursuit of performance, while the inherent data heterogeneity across centers or populations induces the conflict. Conventional multi-task learning paradigms offer a promising framework; however, they fail to consider critical meta information (e.g., site-specific acquisition and modality availability) to combat the heterogeneity. To address this challenge, we propose a Collaborative Meta Knowledge Enhancement (COME) framework for dementia etiology diagnosis, which injects multi-center acquisition semantics, source identifiers, and modality indicators as heterogeneity-aware embeddings into a unified Transformer architecture for scale-up training, enabling explicit modeling of heterogeneity. Besides, a trust-region constrained optimization scheme is designed to regularize the model from spurious correlations during training through a reference model. Across seven independent cohorts, our method achieves state-of-the-art in-domain performance with a mean macro-averaged AUC of 85.62% and a 4.29-point gain over the strongest baseline, while maintaining superior out-of-domain generalization under both cross-center and cross-sequence evaluations. Extensive validation also confirms the alignment between model predictions and established biomarkers (amyloid, tau) and clinical severity, highlighting the potential of COME to enable robust and interpretable dementia diagnostics in real-world settings.
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