Literature DB >> 25797843

Capturing subject variability in fMRI data: A graph-theoretical analysis of GICA vs. IVA.

Jonathan Laney1, Kelly P Westlake2, Sai Ma3, Elizabeth Woytowicz2, Vince D Calhoun4, Tülay Adalı3.   

Abstract

BACKGROUND: Recent studies using simulated functional magnetic resonance imaging (fMRI) data show that independent vector analysis (IVA) is a superior solution for capturing spatial subject variability when compared with the widely used group independent component analysis (GICA). Retaining such variability is of fundamental importance for identifying spatially localized group differences in intrinsic brain networks. NEW
METHODS: Few studies on capturing subject variability and order selection have evaluated real fMRI data. Comparison of multivariate components generated by multiple algorithms is not straightforward. The main difficulties are finding concise methods to extract meaningful features and comparing multiple components despite lack of a ground truth. In this paper, we present a graph-theoretical (GT) approach to effectively compare the ability of multiple multivariate algorithms to capture subject variability for real fMRI data for effective group comparisons. The GT approach is applied to components generated from fMRI data, collected from individuals with stroke, before and after a rehabilitation intervention. COMPARISON WITH EXISTING
METHOD: IVA is compared with widely used GICA for the purpose of group discrimination in terms of GT features. In addition, masks are applied for motor related components generated by both algorithms.
CONCLUSIONS: Results show that IVA better captures subject variability producing more activated voxels and generating components with less mutual information in the spatial domain than Group ICA. IVA-generated components result in smaller p-values and clearer trends in GT features.
Copyright © 2015 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  GICA; Graph-theoretical analysis; IVA; Order selection; Stroke patient; fMRI

Mesh:

Year:  2015        PMID: 25797843      PMCID: PMC4961734          DOI: 10.1016/j.jneumeth.2015.03.019

Source DB:  PubMed          Journal:  J Neurosci Methods        ISSN: 0165-0270            Impact factor:   2.390


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