Supervised Discriminative Group Sparse Representation for Mild Cognitive Impairment Diagnosis.

Journal Article (Journal Article)

Research on an early detection of Mild Cognitive Impairment (MCI), a prodromal stage of Alzheimer's Disease (AD), with resting-state functional Magnetic Resonance Imaging (rs-fMRI) has been of great interest for the last decade. Witnessed by recent studies, functional connectivity is a useful concept in extracting brain network features and finding biomarkers for brain disease diagnosis. However, it still remains challenging for the estimation of functional connectivity from rs-fMRI due to the inevitable high dimensional problem. In order to tackle this problem, we utilize a group sparse representation along with a structural equation model. Unlike the conventional group sparse representation method that does not explicitly consider class-label information, which can help enhance the diagnostic performance, in this paper, we propose a novel supervised discriminative group sparse representation method by penalizing a large within-class variance and a small between-class variance of connectivity coefficients. Thanks to the newly devised penalization terms, we can learn connectivity coefficients that are similar within the same class and distinct between classes, thus helping enhance the diagnostic accuracy. The proposed method also allows the learned common network structure to preserve the network specific and label-related characteristics. In our experiments on the rs-fMRI data of 37 subjects (12 MCI; 25 healthy normal control) with a cross-validation technique, we demonstrated the validity and effectiveness of the proposed method, showing the diagnostic accuracy of 89.19 % and the sensitivity of 0.9167.

Full Text

Duke Authors

Cited Authors

  • Suk, H-I; Wee, C-Y; Lee, S-W; Shen, D

Published Date

  • July 2015

Published In

Volume / Issue

  • 13 / 3

Start / End Page

  • 277 - 295

PubMed ID

  • 25501275

Pubmed Central ID

  • PMC4469635

Electronic International Standard Serial Number (EISSN)

  • 1559-0089

Digital Object Identifier (DOI)

  • 10.1007/s12021-014-9241-6


  • eng

Conference Location

  • United States