TY - JOUR
T1 - A novel matrix-similarity based loss function for joint regression and classification in AD diagnosis
AU - Zhu, Xiaofeng
AU - Suk, Heung Il
AU - Shen, Dinggang
N1 - Funding Information:
Many thanks for the constructive advice from Feng Liu, Guan Yu, and Kim-Han Thung. This study was supported by National Institutes of Health ( EB006733 , EB008374 , EB009634 , AG041721 , AG042599 , and MH100217 ). Xiaofeng Zhu was partly supported by the National Natural Science Foundation of China under grant 61263035 .
PY - 2014/10/15
Y1 - 2014/10/15
N2 - Recent studies on AD/MCI diagnosis have shown that the tasks of identifying brain disease and predicting clinical scores are highly related to each other. Furthermore, it has been shown that feature selection with a manifold learning or a sparse model can handle the problems of high feature dimensionality and small sample size. However, the tasks of clinical score regression and clinical label classification were often conducted separately in the previous studies. Regarding the feature selection, to our best knowledge, most of the previous work considered a loss function defined as an element-wise difference between the target values and the predicted ones. In this paper, we consider the problems of joint regression and classification for AD/MCI diagnosis and propose a novel matrix-similarity based loss function that uses high-level information inherent in the target response matrix and imposes the information to be preserved in the predicted response matrix. The newly devised loss function is combined with a group lasso method for joint feature selection across tasks, i.e., predictions of clinical scores and a class label. In order to validate the effectiveness of the proposed method, we conducted experiments on the Alzheimer's Disease Neuroimaging Initiative (ADNI) dataset, and showed that the newly devised loss function helped enhance the performances of both clinical score prediction and disease status identification, outperforming the state-of-the-art methods.
AB - Recent studies on AD/MCI diagnosis have shown that the tasks of identifying brain disease and predicting clinical scores are highly related to each other. Furthermore, it has been shown that feature selection with a manifold learning or a sparse model can handle the problems of high feature dimensionality and small sample size. However, the tasks of clinical score regression and clinical label classification were often conducted separately in the previous studies. Regarding the feature selection, to our best knowledge, most of the previous work considered a loss function defined as an element-wise difference between the target values and the predicted ones. In this paper, we consider the problems of joint regression and classification for AD/MCI diagnosis and propose a novel matrix-similarity based loss function that uses high-level information inherent in the target response matrix and imposes the information to be preserved in the predicted response matrix. The newly devised loss function is combined with a group lasso method for joint feature selection across tasks, i.e., predictions of clinical scores and a class label. In order to validate the effectiveness of the proposed method, we conducted experiments on the Alzheimer's Disease Neuroimaging Initiative (ADNI) dataset, and showed that the newly devised loss function helped enhance the performances of both clinical score prediction and disease status identification, outperforming the state-of-the-art methods.
KW - Alzheimer's disease (AD)
KW - Feature selection
KW - Joint sparse learning
KW - Manifold learning
KW - Mild Cognitive Impairment (MCI) conversion
UR - http://www.scopus.com/inward/record.url?scp=84903899707&partnerID=8YFLogxK
U2 - 10.1016/j.neuroimage.2014.05.078
DO - 10.1016/j.neuroimage.2014.05.078
M3 - Article
C2 - 24911377
AN - SCOPUS:84903899707
SN - 1053-8119
VL - 100
SP - 91
EP - 105
JO - NeuroImage
JF - NeuroImage
ER -