Staging and Pseudotime Inference of Alzheimer's Disease Progression using Multimodal Imaging Data.

Akira A Nair, Zixuan Wen, Zexuan Wang, Jingwen Yan, Andrew J Saykin, Heng Huang, Paul M Thompson, Christos Davatzikos, Li Shen
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Abstract

Alzheimer's disease (AD) is a neurodegenerative disorder characterized by progressive cognitive decline, driven by the accumulation of amyloid-beta plaques, tau tangles, and neuronal atrophy. This study analyzes three imaging modalities corresponding to the three hallmark biomarkers of AD: amyloid PET, tau PET, and structural MRI. Using cortical measurements from the ADNI dataset, we apply PHATE (Potential of Heat-diffusion for Affinity-based Trajectory Embedding), a dimensionality reduction technique, to uncover continuous trajectories of disease progression. We derive pseudotime values from PHATE embeddings via Slingshot, a principal-curve-based pseudotime inference algorithm. In parallel, we apply SuStaIn (Subtype and Stage Inference), a machine learning model that uncovers distinct biomarker event sequences and assigns subjects to discrete disease stages. We observe strong correspondence between SuStaIn-predicted stages and PHATE-derived pseudotimes, indicating temporal coherence across modeling frameworks. SuStaIn further reveals non-overlapping, modality-specific sequences of biomarker abnormalities, consistent with prior neuropathological models. We validate these sequences using pseudotime-aligned kernel density models and clinical measures. Together, our results support the integrative use of these approaches for evaluating AD progression. Future steps will focus on anchoring pseudotime to real-world clinical timelines and experimentally validating SuStaIn-predicted biomarker cascades.

利用多模态成像数据对阿尔茨海默病进展的分期和伪时间推断。
阿尔茨海默病(AD)是一种神经退行性疾病,其特征是由淀粉样斑块、tau缠结和神经元萎缩的积累引起的进行性认知能力下降。本研究分析了与AD的三个标志性生物标志物相对应的三种成像方式:淀粉样蛋白PET、tau PET和结构MRI。使用来自ADNI数据集的皮质测量,我们应用PHATE(基于亲和的轨迹嵌入的热扩散潜力),一种降维技术,来揭示疾病进展的连续轨迹。我们通过Slingshot(一种基于主曲线的伪时间推断算法)从PHATE嵌入中导出伪时间值。与此同时,我们应用了SuStaIn (Subtype and Stage Inference),这是一种机器学习模型,可以揭示不同的生物标志物事件序列,并将受试者分配到离散的疾病阶段。我们观察到在sustain预测的阶段和phate衍生的伪时间之间有很强的对应关系,表明建模框架之间的时间一致性。SuStaIn进一步揭示了生物标志物异常的非重叠、模式特异性序列,与先前的神经病理模型一致。我们使用伪时间对齐核密度模型和临床测量验证这些序列。总之,我们的结果支持综合使用这些方法来评估阿尔茨海默病的进展。未来的步骤将集中在将假时间锚定到现实世界的临床时间表上,并通过实验验证可持续预测的生物标志物级联。
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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