Sayantan Kumar, Philip R O Payne, Aristeidis Sotiras
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To address this limitation, we propose a multi-modal variational autoencoder (mmVAE) based normative modelling framework that can capture the joint distribution between different modalities to identify abnormal brain volume deviations due to AD. Our multi-modal framework takes as input Freesurfer processed brain region volumes from T1-weighted (cortical and subcortical) and T2-weighed (hippocampal) scans of cognitively normal participants to learn the morphological characteristics of the healthy brain. The estimated normative model is then applied on AD patients to quantify the deviation in brain volumes and identify abnormal brain pattern deviations due to the progressive stages of AD. We compared our proposed mmVAE with a baseline unimodal VAE having a single encoder and decoder and the two modalities concatenated as unimodal input. 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引用次数: 0
摘要
常模是了解阿尔茨海默病(AD)等脑部疾病潜在异质性的一种方法,它通过量化每位患者如何偏离从健康对照分布中学到的预期常模。现有的基于深度学习的常模模型仅应用于单模态磁共振成像(MRI)神经成像数据。然而,这些模型没有考虑到多模态磁共振成像提供的互补信息,而这些信息对于理解像 AD 这样的多因素疾病至关重要。为了解决这一局限性,我们提出了一种基于多模态变异自动编码器(mmVAE)的规范建模框架,该框架可以捕捉不同模态之间的联合分布,从而识别由于注意力缺失症导致的异常脑容量偏差。我们的多模态框架将来自认知正常参与者的 T1 加权(皮质和皮质下)和 T2 加权(海马)扫描的 Freesurfer 处理过的脑区体积作为输入,以学习健康大脑的形态特征。然后将估算出的常模应用于注意力缺失症患者,以量化脑容量的偏差,并识别注意力缺失症进展阶段导致的异常脑形态偏差。我们将所提出的 mmVAE 与基线单模态 VAE 进行了比较,后者只有一个编码器和解码器,两种模态合并为单模态输入。我们的实验结果表明,与单模态基线模型相比,mmVAE 生成的偏差图对 AD 的疾病分期更敏感,与患者认知的相关性更好,并能生成更多具有统计意义的偏差脑区。
Normative Modeling using Multimodal Variational Autoencoders to Identify Abnormal Brain Volume Deviations in Alzheimer's Disease.
Normative modelling is a method for understanding the underlying heterogeneity within brain disorders like Alzheimer Disease (AD), by quantifying how each patient deviates from the expected normative pattern that has been learned from a healthy control distribution. Existing deep learning based normative models have been applied on only single modality Magnetic Resonance Imaging (MRI) neuroimaging data. However, these do not take into account the complementary information offered by multimodal M RI, which is essential for understanding a multifactorial disease like AD. To address this limitation, we propose a multi-modal variational autoencoder (mmVAE) based normative modelling framework that can capture the joint distribution between different modalities to identify abnormal brain volume deviations due to AD. Our multi-modal framework takes as input Freesurfer processed brain region volumes from T1-weighted (cortical and subcortical) and T2-weighed (hippocampal) scans of cognitively normal participants to learn the morphological characteristics of the healthy brain. The estimated normative model is then applied on AD patients to quantify the deviation in brain volumes and identify abnormal brain pattern deviations due to the progressive stages of AD. We compared our proposed mmVAE with a baseline unimodal VAE having a single encoder and decoder and the two modalities concatenated as unimodal input. Our experimental results show that deviation maps generated by mmVAE are more sensitive to disease staging within AD, have a better correlation with patient cognition and result in higher number of brain regions with statistically significant deviations compared to the unimodal baseline model.