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      Analysis of fMRI data by blind separation into independent spatial components

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          Abstract

          Current analytical techniques applied to functional magnetic resonance imaging (fMRI) data require a priori knowledge or specific assumptions about the time courses of processes contributing to the measured signals. Here we describe a new method for analyzing fMRI data based on the independent component analysis (ICA) algorithm of Bell and Sejnowski ([1995]: Neural Comput 7:1129–1159). We decomposed eight fMRI data sets from 4 normal subjects performing Stroop color‐naming, the Brown and Peterson word/number task, and control tasks into spatially independent components. Each component consisted of voxel values at fixed three‐dimensional locations (a component “map”), and a unique associated time course of activation. Given data from 144 time points collected during a 6‐min trial, ICA extracted an equal number of spatially independent components. In all eight trials, ICA derived one and only one component with a time course closely matching the time course of 40‐sec alternations between experimental and control tasks. The regions of maximum activity in these consistently task‐related components generally overlapped active regions detected by standard correlational analysis, but included frontal regions not detected by correlation. Time courses of other ICA components were transiently task‐related, quasiperiodic, or slowly varying. By utilizing higher‐order statistics to enforce successively stricter criteria for spatial independence between component maps, both the ICA algorithm and a related fourth‐order decomposition technique (Comon [1994]: Signal Processing 36:11–20) were superior to principal component analysis (PCA) in determining the spatial and temporal extent of task‐related activation. For each subject, the time courses and active regions of the task‐related ICA components were consistent across trials and were robust to the addition of simulated noise. Simulated movement artifact and simulated task‐related activations added to actual fMRI data were clearly separated by the algorithm. ICA can be used to distinguish between nontask‐related signal components, movements, and other artifacts, as well as consistently or transiently task‐related fMRI activations, based on only weak assumptions about their spatial distributions and without a priori assumptions about their time courses. ICA appears to be a highly promising method for the analysis of fMRI data from normal and clinical populations, especially for uncovering unpredictable transient patterns of brain activity associated with performance of psychomotor tasks. Hum. Brain Mapping 6:160–188, 1998. © 1998 Wiley‐Liss, Inc.

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          Author and article information

          Contributors
          martin@salk.edu
          Journal
          Hum Brain Mapp
          Hum Brain Mapp
          10.1002/(ISSN)1097-0193
          HBM
          Human Brain Mapping
          John Wiley & Sons, Inc. (New York )
          1065-9471
          1097-0193
          07 December 1998
          1998
          : 6
          : 3 ( doiID: 10.1002/(SICI)1097-0193(1998)6:3<>1.0.CO;2-S )
          : 160-188
          Affiliations
          [ 1 ]Howard Hughes Medical Institute, Computational Neurobiology Laboratory, Salk Institute for Biological Studies, La Jolla, California 92186‐5800
          [ 2 ]Cognitive Psychophysiology Laboratory, Naval Health Research Center, San Diego, California 92186‐5122
          [ 3 ]Department of Neurosciences, School of Medicine, University of California at San Diego, La Jolla, California 92093
          [ 4 ]Department of Psychiatry, School of Medicine, University of California at San Diego, La Jolla, California 92093
          [ 5 ]Department of Biology, University of California at San Diego, La Jolla, California 92093
          Author notes
          [*] [* ]Computational Neurobiology Laboratory, Salk Institute for Biological Studies, 10010 North Torrey Pines Road, La Jolla, CA 92037‐1099
          Article
          PMC6873377 PMC6873377 6873377 HBM5
          10.1002/(SICI)1097-0193(1998)6:3<160::AID-HBM5>3.0.CO;2-1
          6873377
          9673671
          6e475d23-ef62-4017-aa7d-bfb5cc2d6cf7
          Copyright © 1998 Wiley‐Liss, Inc.
          History
          : 02 June 1997
          : 13 January 1998
          Page count
          Figures: 23, Tables: 0, References: 42, Pages: 29, Words: 14350
          Funding
          Funded by: Heart and Stroke Foundation of Ontario
          Funded by: Howard Hughes Medical Institute
          Funded by: U.S. Office of Naval Research
          Categories
          Article
          Custom metadata
          2.0
          1998
          Converter:WILEY_ML3GV2_TO_JATSPMC version:5.7.2 mode:remove_FC converted:15.11.2019

          higher‐order statistics,independent component analysis,functional magnetic resonance imaging

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