Feature Learning and Fusion of Multimodality Neuroimaging and Genetic Data for Multi-status Dementia Diagnosis.

Tao Zhou, Kim-Han Thung, Xiaofeng Zhu, Dinggang Shen
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引用次数: 24

Abstract

In this paper, we aim to maximally utilize multimodality neuroimaging and genetic data to predict Alzheimer's disease (AD) and its prodromal status, i.e., a multi-status dementia diagnosis problem. Multimodality neuroimaging data such as MRI and PET provide valuable insights to abnormalities, and genetic data such as Single Nucleotide Polymorphism (SNP) provide information about a patient's AD risk factors. When used in conjunction, AD diagnosis may be improved. However, these data are heterogeneous (e.g., having different data distributions), and have different number of samples (e.g., PET data is having far less number of samples than the numbers of MRI or SNPs). Thus, learning an effective model using these data is challenging. To this end, we present a novel three-stage deep feature learning and fusion framework , where the deep neural network is trained stage-wise. Each stage of the network learns feature representations for different combination of modalities, via effective training using maximum number of available samples . Specifically, in the first stage, we learn latent representations (i.e., high-level features) for each modality independently, so that the heterogeneity between modalities can be better addressed and then combined in the next stage. In the second stage, we learn the joint latent features for each pair of modality combination by using the high-level features learned from the first stage. In the third stage, we learn the diagnostic labels by fusing the learned joint latent features from the second stage. We have tested our framework on Alzheimer's Disease Neuroimaging Initiative (ADNI) dataset for multi-status AD diagnosis, and the experimental results show that the proposed framework outperforms other methods.

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特征学习和多模态神经影像学与遗传数据融合用于多状态痴呆诊断。
在本文中,我们旨在最大限度地利用多模态神经影像学和遗传学数据来预测阿尔茨海默病(AD)及其前体状态,即多状态痴呆诊断问题。MRI和PET等多模态神经成像数据为异常提供了有价值的见解,而单核苷酸多态性(SNP)等遗传数据提供了有关患者AD风险因素的信息。当结合使用时,AD的诊断可能会得到改善。然而,这些数据是异构的(例如,具有不同的数据分布),并且具有不同的样本数量(例如,PET数据的样本数量远远少于MRI或snp的数量)。因此,使用这些数据学习一个有效的模型是具有挑战性的。为此,我们提出了一种新的三阶段深度特征学习和融合框架,其中深度神经网络是分阶段训练的。网络的每个阶段通过使用最大可用样本数量的有效训练来学习不同模态组合的特征表示。具体来说,在第一阶段,我们独立学习每个模态的潜在表征(即高级特征),以便更好地解决模态之间的异质性,然后在下一阶段进行组合。在第二阶段,我们利用从第一阶段学习到的高级特征来学习每对模态组合的联合潜在特征。在第三阶段,我们通过融合从第二阶段学习到的关节潜在特征来学习诊断标签。我们在ADNI数据集上对该框架进行了多状态AD诊断测试,实验结果表明该框架优于其他方法。
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Probabilistic 3D Correspondence Prediction from Sparse Unsegmented Images. Class-Balanced Deep Learning with Adaptive Vector Scaling Loss for Dementia Stage Detection. MoViT: Memorizing Vision Transformers for Medical Image Analysis. Robust Unsupervised Super-Resolution of Infant MRI via Dual-Modal Deep Image Prior. IA-GCN: Interpretable Attention based Graph Convolutional Network for Disease Prediction.
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