Manifold regularized multitask feature learning for multimodality disease classification

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 modali...

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Bibliographic Details
Published inHuman brain mapping Vol. 36; no. 2; pp. 489 - 507
Main Authors Jie, Biao, Zhang, Daoqiang, Cheng, Bo, Shen, Dinggang
Format Journal Article
LanguageEnglish
Published United States Blackwell Publishing Ltd 01.02.2015
John Wiley & Sons, Inc
John Wiley and Sons Inc
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Summary: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. © 2014 Wiley Periodicals, Inc.
Bibliography:istex:DE2C348E4671A776D1A8B4EFCF1ED5255616E230
the NUAA Fundamental Research Funds - No. NE2013105
National Institutes of Health Grant - No. U01 AG024904
NIH grants - No. EB006733; No. EB008374; No. EB009634; No. AG041721
ArticleID:HBM22642
ark:/67375/WNG-2JS5QJMN-F
National Natural Science Foundation of China - No. 61422204; No. 61473149
the Jiangsu Natural Science Foundation for Distinguished Young Scholar - No. BK20130034
the Specialized Research Fund for the Doctoral Program of Higher Education - No. 20123218110009
the National Institute on Aging; the National Institute of Biomedical Imaging and Bioengineering; Abbott; AstraZeneca AB; Bayer Schering Pharma AG; Bristol-Myers Squibb; Eisai Global Clinical Development; Elan Corporation; Genentech; GE Healthcare; GlaxoSmithKline; Innogenetics; Johnson and Johnson; Eli Lilly and Co.; Medpace, Inc.; Merck and Co., Inc.; Novartis AG, Pfizer Inc; F. Hoffman-La Roche; Schering-Plough; Synarc, Inc.; as well as non-profit partners the Alzheimer's Association and Alzheimer's Drug Discovery Foundation, with participation from the U.S. Food and Drug Administration; Foundation for the National Institutes of Health (www.fnih.org) (ADNI)
As such, the investigators within the ADNI contributed to the design and implementation of ADNI and/or provided data but did not participate in analysis or writing of this report. A complete listing of ADNI investigators can be found at
www.loni.ucla.edu/ADNI/Collaboration/ADNI_Authorship_list.pdf
Data used in preparation of this article were obtained from the Alzheimer's Disease Neuroimaging Initiative (ADNI) database
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www.loni.ucla.edu/ADNI
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Data used in preparation of this article were obtained from the Alzheimer's Disease Neuroimaging Initiative (ADNI) database (http://www.loni.ucla.edu/ADNI). As such, the investigators within the ADNI contributed to the design and implementation of ADNI and/or provided data but did not participate in analysis or writing of this report. A complete listing of ADNI investigators can be found at: http://www.loni.ucla.edu/ADNI/Collaboration/ADNI_Authorship_list.pdf.
ISSN:1065-9471
1097-0193
1097-0193
DOI:10.1002/hbm.22642