TY - JOUR
T1 - Enriched white matter connectivity networks for accurate identification of MCI patients
AU - Wee, Chong Yaw
AU - Yap, Pew Thian
AU - Li, Wenbin
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:
The authors wish to thank the anonymous reviewers for their valuable comments. This work was supported in part by NIH grants EB006733 , EB008760 , MH076970 , EB009634 , NIA L30-AG029001 , P30 AG028377-02 , K23-AG028982 , as well as a National Alliance for Research in Schizophrenia and Depression Young Investigator Award (LW), a Science and Technology Commission of Shanghai Municipality grant (STCSM; Grant No. 08411951200 ), National Basic Research Program of China (973 Program, Grant No. 2010CB732505 ).
PY - 2011/2/1
Y1 - 2011/2/1
N2 - Mild cognitive impairment (MCI), often a prodromal phase of Alzheimer's disease (AD), is frequently considered to be a good target for early diagnosis and therapeutic interventions of AD. Recent emergence of reliable network characterization techniques has made it possible to understand neurological disorders at a whole-brain connectivity level. Accordingly, we propose an effective network-based multivariate classification algorithm, using a collection of measures derived from white matter (WM) connectivity networks, to accurately identify MCI patients from normal controls. An enriched description of WM connections, utilizing six physiological parameters, i.e., fiber count, fractional anisotropy (FA), mean diffusivity (MD), and principal diffusivities(Λ1, Λ2, and Λ3), results in six connectivity networks for each subject to account for the connection topology and the biophysical properties of the connections. Upon parcellating the brain into 90 regions-of-interest (ROIs), these properties can be quantified for each pair of regions with common traversing fibers. For building an MCI classifier, clustering coefficient of each ROI in relation to the remaining ROIs is extracted as feature for classification. These features are then ranked according to their Pearson correlation with respect to the clinical labels, and are further sieved to select the most discriminant subset of features using an SVM-based feature selection algorithm. Finally, support vector machines (SVMs) are trained using the selected subset of features. Classification accuracy was evaluated via leave-one-out cross-validation to ensure generalization of performance. The classification accuracy given by our enriched description of WM connections is 88.9%, which is an increase of at least 14.8% from that using simple WM connectivity description with any single physiological parameter. A cross-validation estimation of the generalization performance shows an area of 0.929 under the receiver operating characteristic (ROC) curve, indicating excellent diagnostic power. It was also found, based on the selected features, that portions of the prefrontal cortex, orbitofrontal cortex, parietal lobe and insula regions provided the most discriminant features for classification, in line with results reported in previous studies. Our MCI classification framework, especially the enriched description of WM connections, allows accurate early detection of brain abnormalities, which is of paramount importance for treatment management of potential AD patients.
AB - Mild cognitive impairment (MCI), often a prodromal phase of Alzheimer's disease (AD), is frequently considered to be a good target for early diagnosis and therapeutic interventions of AD. Recent emergence of reliable network characterization techniques has made it possible to understand neurological disorders at a whole-brain connectivity level. Accordingly, we propose an effective network-based multivariate classification algorithm, using a collection of measures derived from white matter (WM) connectivity networks, to accurately identify MCI patients from normal controls. An enriched description of WM connections, utilizing six physiological parameters, i.e., fiber count, fractional anisotropy (FA), mean diffusivity (MD), and principal diffusivities(Λ1, Λ2, and Λ3), results in six connectivity networks for each subject to account for the connection topology and the biophysical properties of the connections. Upon parcellating the brain into 90 regions-of-interest (ROIs), these properties can be quantified for each pair of regions with common traversing fibers. For building an MCI classifier, clustering coefficient of each ROI in relation to the remaining ROIs is extracted as feature for classification. These features are then ranked according to their Pearson correlation with respect to the clinical labels, and are further sieved to select the most discriminant subset of features using an SVM-based feature selection algorithm. Finally, support vector machines (SVMs) are trained using the selected subset of features. Classification accuracy was evaluated via leave-one-out cross-validation to ensure generalization of performance. The classification accuracy given by our enriched description of WM connections is 88.9%, which is an increase of at least 14.8% from that using simple WM connectivity description with any single physiological parameter. A cross-validation estimation of the generalization performance shows an area of 0.929 under the receiver operating characteristic (ROC) curve, indicating excellent diagnostic power. It was also found, based on the selected features, that portions of the prefrontal cortex, orbitofrontal cortex, parietal lobe and insula regions provided the most discriminant features for classification, in line with results reported in previous studies. Our MCI classification framework, especially the enriched description of WM connections, allows accurate early detection of brain abnormalities, which is of paramount importance for treatment management of potential AD patients.
KW - Alzheimer's disease (AD)
KW - Connectivity network
KW - Enriched connectivity
KW - Mild cognitive impairment (MCI)
KW - Support vector machines (SVMs)
KW - White matter (WM)
UR - http://www.scopus.com/inward/record.url?scp=78650237923&partnerID=8YFLogxK
U2 - 10.1016/j.neuroimage.2010.10.026
DO - 10.1016/j.neuroimage.2010.10.026
M3 - Article
C2 - 20970508
AN - SCOPUS:78650237923
SN - 1053-8119
VL - 54
SP - 1812
EP - 1822
JO - NeuroImage
JF - NeuroImage
IS - 3
ER -