Manifold Regularized Multitask Feature Learning for Multimodality Disease Classification

被引:131
作者
Jie, Biao [1 ,2 ]
Zhang, Daoqiang [1 ]
Cheng, Bo [1 ]
Shen, Dinggang [3 ,4 ,5 ]
机构
[1] Nanjing Univ Aeronaut & Astronaut, Dept Comp Sci & Engn, Nanjing 210016, Jiangsu, Peoples R China
[2] Anhui Normal Univ, Dept Comp Sci & Technol, Wuhu, Peoples R China
[3] Univ N Carolina, Dept Radiol, Chapel Hill, NC USA
[4] Univ N Carolina, BRIC, Chapel Hill, NC USA
[5] Korea Univ, Dept Brain & Cognit Engn, Seoul, South Korea
基金
中国国家自然科学基金; 美国国家卫生研究院;
关键词
manifold regularization; group-sparsity regularizer; multitask learning; feature selection; multimodality classification; Alzheimer's disease; MILD COGNITIVE IMPAIRMENT; EARLY ALZHEIMERS-DISEASE; FDG-PET; FRONTOTEMPORAL DEMENTIA; CSF BIOMARKERS; ATROPHY; MCI; SELECTION; MACHINE; MODEL;
D O I
10.1002/hbm.22642
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Multimodality based methods have shown great advantages in classification of Alzheimer's disease (AD) and its prodromal stage, that is, mild cognitive impairment (MCI). Recently, multitask feature selection methods are typically used for joint selection of common features across multiple modalities. However, one disadvantage of existing multimodality based methods is that they ignore the useful data distribution information in each modality, which is essential for subsequent classification. Accordingly, in this paper we propose a manifold regularized multitask feature learning method to preserve both the intrinsic relatedness among multiple modalities of data and the data distribution information in each modality. Specifically, we denote the feature learning on each modality as a single task, and use group-sparsity regularizer to capture the intrinsic relatedness among multiple tasks (i.e., modalities) and jointly select the common features from multiple tasks. Furthermore, we introduce a new manifold-based Laplacian regularizer to preserve the data distribution information from each task. Finally, we use the multikernel support vector machine method to fuse multimodality data for eventual classification. Conversely, we also extend our method to the semisupervised setting, where only partial data are labeled. We evaluate our method using the baseline magnetic resonance imaging (MRI), fluorodeoxyglucose positron emission tomography (FDG-PET), and cerebrospinal fluid (CSF) data of subjects from AD neuroimaging initiative database. The experimental results demonstrate that our proposed method can not only achieve improved classification performance, but also help to discover the disease-related brain regions useful for disease diagnosis. Hum Brain Mapp 36:489-507, 2015. (c) 2014 Wiley Periodicals, Inc.
引用
收藏
页码:489 / 507
页数:19
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