TY - JOUR
T1 - Identification of MCI individuals using structural and functional connectivity networks
AU - Wee, Chong Yaw
AU - Yap, Pew Thian
AU - Zhang, Daoqiang
AU - Denny, Kevin
AU - Browndyke, Jeffrey N.
AU - Potter, Guy G.
AU - Welsh-Bohmer, Kathleen A.
AU - Wang, Lihong
AU - Shen, Dinggang
N1 - Funding Information:
This work was supported in part by NIH grants EB006733, EB008374, EB009634, MH088520, NIA L30-AG029001, P30 AG028377-02, K23-AG028982 , as well as a National Alliance for Research in Schizophrenia and Depression Young Investigator Award (LW).
PY - 2012/2/1
Y1 - 2012/2/1
N2 - Different imaging modalities provide essential complementary information that can be used to enhance our understanding of brain disorders. This study focuses on integrating multiple imaging modalities to identify individuals at risk for mild cognitive impairment (MCI). MCI, often an early stage of Alzheimer's disease (AD), is difficult to diagnose due to its very mild or insignificant symptoms of cognitive impairment. Recent emergence of brain network analysis has made characterization of neurological disorders at a whole-brain connectivity level possible, thus providing new avenues for brain diseases classification. Employing multiple-kernel Support Vector Machines (SVMs), we attempt to integrate information from diffusion tensor imaging (DTI) and resting-state functional magnetic resonance imaging (rs-fMRI) for improving classification performance. Our results indicate that the multimodality classification approach yields statistically significant improvement in accuracy over using each modality independently. The classification accuracy obtained by the proposed method is 96.3%, which is an increase of at least 7.4% from the single modality-based methods and the direct data fusion method. A cross-validation estimation of the generalization performance gives an area of 0.953 under the receiver operating characteristic (ROC) curve, indicating excellent diagnostic power. The multimodality classification approach hence allows more accurate early detection of brain abnormalities with greater sensitivity.
AB - Different imaging modalities provide essential complementary information that can be used to enhance our understanding of brain disorders. This study focuses on integrating multiple imaging modalities to identify individuals at risk for mild cognitive impairment (MCI). MCI, often an early stage of Alzheimer's disease (AD), is difficult to diagnose due to its very mild or insignificant symptoms of cognitive impairment. Recent emergence of brain network analysis has made characterization of neurological disorders at a whole-brain connectivity level possible, thus providing new avenues for brain diseases classification. Employing multiple-kernel Support Vector Machines (SVMs), we attempt to integrate information from diffusion tensor imaging (DTI) and resting-state functional magnetic resonance imaging (rs-fMRI) for improving classification performance. Our results indicate that the multimodality classification approach yields statistically significant improvement in accuracy over using each modality independently. The classification accuracy obtained by the proposed method is 96.3%, which is an increase of at least 7.4% from the single modality-based methods and the direct data fusion method. A cross-validation estimation of the generalization performance gives an area of 0.953 under the receiver operating characteristic (ROC) curve, indicating excellent diagnostic power. The multimodality classification approach hence allows more accurate early detection of brain abnormalities with greater sensitivity.
KW - Alzheimer's disease (AD)
KW - Brain network analysis multiple-kernel Support Vector Machines (SVMs)
KW - Diffusion tensor imaging (DTI)
KW - Mild cognitive impairment (MCI)
KW - Multimodality representation
KW - Resting-state functional magnetic resonance imaging (rs-fMRI)
UR - http://www.scopus.com/inward/record.url?scp=84855453290&partnerID=8YFLogxK
U2 - 10.1016/j.neuroimage.2011.10.015
DO - 10.1016/j.neuroimage.2011.10.015
M3 - Article
C2 - 22019883
AN - SCOPUS:84855453290
SN - 1053-8119
VL - 59
SP - 2045
EP - 2056
JO - NeuroImage
JF - NeuroImage
IS - 3
ER -