Department of Electrical and Computer Engineering, Sungkyunkwan University, Suwon, Korea; Center for Neuroscience Imaging Research, Institute for Basic Science, Suwon, Korea.
Department of Neurology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea; Neuroscience Center, Samsung Medical Center, Seoul, Korea.
Med Image Anal. 2022 Apr;77:102378. doi: 10.1016/j.media.2022.102378. Epub 2022 Jan 29.
Neuroimaging genetics is a powerful approach to jointly explore genetic features with rich brain imaging phenotypes for neurodegenerative diseases. Conventional imaging genetics approaches based on canonical correlation analysis cannot accommodate multimodal inputs effectively and have limited interpretability. We propose a novel imaging genetics approach based on non-negative matrix factorization (NMF). By leveraging the parsimonious property known as topic modeling in multi-view NMF, we add sparsity constraints and prior information to identify a sparse set of biologically related features across modalities. Thus, our approach incorporates prior knowledge and improves multimodal integration capabilities and interpretability. We applied our algorithm to simulated and real imaging genetics datasets of Parkinson's disease (PD) for performance evaluation. Our algorithm could identify important associated features mapped to interpretable distinct topics more robustly than other methods. It revealed promising features of single-nucleotide polymorphisms and brain regions related to a subset of PD-related clinical scores in a few topics using a real imaging genetic dataset. The proposed imaging genetics approach can reveal novel associations between genetic and neuroimaging features to improve understanding of various neurodegenerative diseases.
神经影像学遗传学是一种强大的方法,可以联合探索神经退行性疾病的遗传特征和丰富的大脑影像表型。基于典型相关分析的传统影像遗传学方法不能有效地适应多模态输入,并且解释能力有限。我们提出了一种基于非负矩阵分解 (NMF) 的新的影像遗传学方法。通过利用多视图 NMF 中称为主题建模的简约特性,我们添加了稀疏约束和先验信息,以识别模态之间具有生物学相关性的稀疏特征集。因此,我们的方法结合了先验知识,提高了多模态集成能力和可解释性。我们将我们的算法应用于帕金森病 (PD) 的模拟和真实影像遗传学数据集进行性能评估。与其他方法相比,我们的算法能够更稳健地识别映射到可解释的不同主题的重要相关特征。它使用真实的影像遗传学数据集在少数几个主题中揭示了与 PD 相关的临床评分子集相关的单核苷酸多态性和大脑区域的有前途的特征。所提出的影像遗传学方法可以揭示遗传和神经影像学特征之间的新关联,从而提高对各种神经退行性疾病的理解。