Multi-modal multi-task learning for joint prediction of multiple regression and classification variables in Alzheimer's disease

被引:527
作者
Zhang, Daoqiang [1 ,2 ,3 ]
Shen, Dinggang [1 ,2 ]
机构
[1] Univ N Carolina, Dept Radiol, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, BRIC, Chapel Hill, NC 27599 USA
[3] Nanjing Univ Aeronaut & Astronaut, Dept Comp Sci & Engn, Nanjing 210016, Jiangsu, Peoples R China
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
Alzheimer's disease (AD); Multi-modal multi-task (M3T) learning; Multi-task feature selection; Multi-modality; MCI conversion; MMSE; ADAS-Cog; MILD COGNITIVE IMPAIRMENT; CSF BIOMARKERS; FDG-PET; BASE-LINE; ATROPHY; MRI; DEMENTIA; DECLINE; VOLUME; MCI;
D O I
10.1016/j.neuroimage.2011.09.069
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Many machine learning and pattern classification methods have been applied to the diagnosis of Alzheimer's disease (AD) and its prodromal stage, i.e., mild cognitive impairment (MCI). Recently, rather than predicting categorical variables as in classification, several pattern regression methods have also been used to estimate continuous clinical variables from brain images. However, most existing regression methods focus on estimating multiple clinical variables separately and thus cannot utilize the intrinsic useful correlation information among different clinical variables. On the other hand, in those regression methods, only a single modality of data (usually only the structural MRI) is often used, without considering the complementary information that can be provided by different modalities. In this paper, we propose a general methodology, namely multimodal multi-task (M3T) learning, to jointly predict multiple variables from multi-modal data. Here, the variables include not only the clinical variables used for regression but also the categorical variable used for classification, with different tasks corresponding to prediction of different variables. Specifically, our method contains two key components, i.e., (1) a multi-task feature selection which selects the common subset of relevant features for multiple variables from each modality, and (2) a multi-modal support vector machine which fuses the above-selected features from all modalities to predict multiple (regression and classification) variables. To validate our method, we perform two sets of experiments on ADNI baseline MRI, FDG-PET, and cerebrospinal fluid (CSF) data from 45 AD patients, 91 MCI patients, and 50 healthy controls (HC). In the first set of experiments, we estimate two clinical variables such as Mini Mental State Examination (MMSE) and Alzheimer's Disease Assessment Scale-Cognitive Subscale (ADAS-Cog), as well as one categorical variable (with value of 'AD', 'MCI' or 'HC'), from the baseline MRI, FDG-PET, and CSF data. In the second set of experiments, we predict the 2-year changes of MMSE and ADAS-Cog scores and also the conversion of MCI to AD from the baseline MRI, FDG-PET, and CSF data. The results on both sets of experiments demonstrate that our proposed M3T learning scheme can achieve better performance on both regression and classification tasks than the conventional learning methods. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:895 / 907
页数:13
相关论文
共 55 条
[41]   Magnetic resonance image tissue classification using a partial volume model [J].
Shattuck, DW ;
Sandor-Leahy, SR ;
Schaper, KA ;
Rottenberg, DA ;
Leahy, RM .
NEUROIMAGE, 2001, 13 (05) :856-876
[42]   Cerebrospinal Fluid Biomarker Signature in Alzheimer's Disease Neuroimaging Initiative Subjects [J].
Shaw, Leslie M. ;
Vanderstichele, Hugo ;
Knapik-Czajka, Malgorzata ;
Clark, Christopher M. ;
Aisen, Paul S. ;
Petersen, Ronald C. ;
Blennow, Kaj ;
Soares, Holly ;
Simon, Adam ;
Lewczuk, Piotr ;
Dean, Robert ;
Siemers, Eric ;
Potter, William ;
Lee, Virginia M. -Y. ;
Trojanowski, John Q. .
ANNALS OF NEUROLOGY, 2009, 65 (04) :403-413
[43]   HAMMER: Hierarchical attribute matching mechanism for elastic registration [J].
Shen, DG ;
Davatzikos, C .
IEEE TRANSACTIONS ON MEDICAL IMAGING, 2002, 21 (11) :1421-1439
[44]   A nonparametric method for automatic correction of intensity nonuniformity in MRI data [J].
Sled, JG ;
Zijdenbos, AP ;
Evans, AC .
IEEE TRANSACTIONS ON MEDICAL IMAGING, 1998, 17 (01) :87-97
[45]   Fast robust automated brain extraction [J].
Smith, SM .
HUMAN BRAIN MAPPING, 2002, 17 (03) :143-155
[46]   Predicting clinical scores from magnetic resonance scans in Alzheimer's disease [J].
Stonnington, Cynthia M. ;
Chu, Carlton ;
Kloeppel, Stefan ;
Jack, Clifford R., Jr. ;
Ashburner, John ;
Frackowiak, Richard S. J. .
NEUROIMAGE, 2010, 51 (04) :1405-1413
[48]   MRI and CSF biomarkers in normal, MCI, and AD subjects Predicting future clinical change [J].
Vemuri, P. ;
Wiste, H. J. ;
Weigand, S. D. ;
Shaw, L. M. ;
Trojanowski, J. Q. ;
Weiner, M. W. ;
Knopman, D. S. ;
Petersen, R. C. ;
Jack, C. R. .
NEUROLOGY, 2009, 73 (04) :294-301
[49]  
Visser PJ, 2002, J NEUROL NEUROSUR PS, V72, P491
[50]   Combining MR Imaging, Positron-Emission Tomography, and CSF Biomarkers in the Diagnosis and Prognosis of Alzheimer Disease [J].
Walhovd, K. B. ;
Fjell, A. M. ;
Brewer, J. ;
McEvoy, L. K. ;
Fennema-Notestine, C. ;
Hagler, D. J., Jr. ;
Jennings, R. G. ;
Karow, D. ;
Dale, A. M. .
AMERICAN JOURNAL OF NEURORADIOLOGY, 2010, 31 (02) :347-354