DocumentCode :
3684906
Title :
Testing different ICA algorithms and connectivity analyses on MS patients
Author :
M Muthuraman;T Anjum;A Droby;V Fleischer;S Reitz;KG Mideksa;G Schmidt;F Zipp;S Groppa
Author_Institution :
Department of Neurology, Christian Albrechts University Kiel, 24105 Germany
fYear :
2015
Firstpage :
4314
Lastpage :
4317
Abstract :
Multiple sclerosis (MS) is a progressive neurological disorder that affects the central nervous system. Functional magnetic resonance imaging (fMRI) has been employed to track the course and disease progression in patients with MS. The two main aims of this study were to apply in a data-driven approach the independent component analysis (ICA) in the spatial domain to depict the active sources and to look at the effective connectivity between the identified spatial sources. Several ICA algorithms have been proposed for fMRI data analysis. In this study, we aimed to test two well characterized algorithms, namely, the fast ICA and the complex infomax algorithms, followed by two effective connectivity algorithms, namely, Granger causality (GC) and generalized partial directed coherence (GPDC), to illustrate the connections between the spatial sources in patients with MS. The results obtained from the ICA analyses showed the involvement of the default mode network sources. The connectivity analyses depicted significant changes between the two applied algorithms. The significance of this study was to demonstrate the robustness of the analyzed algorithms in patients with MS and to validate them before applying them on larger datasets of patients with MS.
Keywords :
"Algorithm design and analysis","Signal processing algorithms","Coherence","Magnetic resonance imaging","Robustness","Time series analysis","Multiple sclerosis"
Publisher :
ieee
Conference_Titel :
Engineering in Medicine and Biology Society (EMBC), 2015 37th Annual International Conference of the IEEE
ISSN :
1094-687X
Electronic_ISBN :
1558-4615
Type :
conf
DOI :
10.1109/EMBC.2015.7319349
Filename :
7319349
Link To Document :
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