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author:

Tong, Tong (Tong, Tong.) [1] | Gray, Katherine (Gray, Katherine.) [2] | Gao, Qinquan (Gao, Qinquan.) [3] | Chen, Liang (Chen, Liang.) [4] | Rueckert, Daniel (Rueckert, Daniel.) [5]

Indexed by:

EI

Abstract:

Accurate diagnosis of Alzheimer's disease (AD) and its prodromal stage mild cognitive impairment (MCI) is of great interest to patients and clinicians. Recent studies have demonstrated that multiple neuroimaging and biological measures contain complementary information for diagnosis and prognosis. Classification methods are needed to combine these multiple biomarkers to provide an accurate diagnosis. State-of-the-art approaches calculate a mixed kernel or a similarity matrix by linearly combining kernels or similarities from multiple modalities. However, the complementary information from multi-modal data are not necessarily linearly related. In addition, this linear combination is also sensitive to the weights assigned to each modality. In this paper, we present a multi-modality classification framework to efficiently exploit the complementarity in the multi-modal data. First, pairwise similarity is calculated for each modality individually using the features including regional MRI volumes, voxel-based FDG-PET signal intensities, CSF biomarker measures, and categorical genetic information. Similarities from multiple modalities are then combined in a nonlinear graph fusion process, which generates a unified graph for final classification. Based on the unified graphs, we achieved classification area under curve (AUC) of receiver-operator characteristic of 98.1% between AD subjects and normal controls (NC), 82.4% between MCI subjects and NC and 77.9% in a three-way classification, which are significantly better than those using single-modality biomarkers and those based on state-of-the-art linear combination approaches. © 2016 Elsevier Ltd

Keyword:

Biomarkers Computer aided diagnosis Genes Learning systems Modal analysis Neurodegenerative diseases Neuroimaging

Community:

  • [ 1 ] [Tong, Tong]Biomedical Image Analysis Group, Department of Computing, Imperial College London, 180 Queen's Gate, London; SW7 2AZ, United Kingdom
  • [ 2 ] [Tong, Tong]Laboratory for Computational Neuroimaging, Athinoula A. Martinos Center for Biomedical Imaging, MGH/Harvard Medical School, Charlestown, United States
  • [ 3 ] [Gray, Katherine]Biomedical Image Analysis Group, Department of Computing, Imperial College London, 180 Queen's Gate, London; SW7 2AZ, United Kingdom
  • [ 4 ] [Gao, Qinquan]Fujian Province Key Lab of Medical Instrument & Pharmaceutical Technology, Fuzhou University, Fuzhou, China
  • [ 5 ] [Chen, Liang]Biomedical Image Analysis Group, Department of Computing, Imperial College London, 180 Queen's Gate, London; SW7 2AZ, United Kingdom
  • [ 6 ] [Rueckert, Daniel]Biomedical Image Analysis Group, Department of Computing, Imperial College London, 180 Queen's Gate, London; SW7 2AZ, United Kingdom

Reprint 's Address:

  • [gao, qinquan]fujian province key lab of medical instrument & pharmaceutical technology, fuzhou university, fuzhou, china

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Source :

Pattern Recognition

ISSN: 0031-3203

Year: 2017

Volume: 63

Page: 171-181

3 . 9 6 2

JCR@2017

7 . 5 0 0

JCR@2023

ESI HC Threshold:177

JCR Journal Grade:1

CAS Journal Grade:2

Cited Count:

WoS CC Cited Count: 0

SCOPUS Cited Count: 185

ESI Highly Cited Papers on the List: 0 Unfold All

WanFang Cited Count:

Chinese Cited Count:

30 Days PV: 0

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