Unified SPM–ICA for fMRI analysis

A widely used tool for functional magnetic resonance imaging (fMRI) data analysis, statistical parametric mapping (SPM), is based on the general linear model (GLM). SPM therefore requires a priori knowledge or specific assumptions about the time courses contributing to signal changes. In contradistinction, independent component analysis (ICA) is a data-driven method based on the assumption that the causes of responses are statistically independent. Here we describe a unified method, which combines ICA, temporal ICA (tICA), and SPM for analyzing fMRI data. tICA was applied to fMRI datasets to disclose independent components, whose number was determined by the Bayesian information criterion (BIC). The resulting components were used to construct the design matrix of a GLM. Parameters were estimated and regionally-specific statistical inferences were made about activations in the usual way. The sensitivity and specificity were evaluated using Monte Carlo simulations. The receiver operating characteristic (ROC) curves indicated that the unified SPM-ICA method had a better performance. Moreover, SPM-ICA was applied to fMRI datasets from twelve normal subjects performing left and right hand movements. The areas identified corresponded to motor (premotor, sensorimotor areas and SMA) areas and were consistently task related. Part of the frontal lobe, parietal cortex, and cingulate gyrus also showed transiently task-related responses. The unified method requires less supervision than the conventional SPM and enables classical inference about the expression of independent components. Our results also suggest that the method has a higher sensitivity than SPM analyses.

[1]  Lars Kai Hansen,et al.  The Quantitative Evaluation of Functional Neuroimaging Experiments: The NPAIRS Data Analysis Framework , 2000, NeuroImage.

[2]  J. Rissanen A UNIVERSAL PRIOR FOR INTEGERS AND ESTIMATION BY MINIMUM DESCRIPTION LENGTH , 1983 .

[3]  Mark W. Woolrich,et al.  Fully Bayesian spatio-temporal modeling of FMRI data , 2004, IEEE Transactions on Medical Imaging.

[4]  B. Biswal,et al.  Blind source separation of multiple signal sources of fMRI data sets using independent component analysis. , 1999, Journal of computer assisted tomography.

[5]  Dewen Hu,et al.  A novel method for spatio-temporal pattern analysis of brain fMRI data , 2005, Science in China Series F: Information Sciences.

[6]  Ying Zheng,et al.  Increased Oxygen Consumption Following Activation of Brain: Theoretical Footnotes Using Spectroscopic Data from Barrel Cortex , 2001, NeuroImage.

[7]  John G. Neuhoff,et al.  Spatiotemporal Pattern of Neural Processing in the Human Auditory Cortex , 2002, Science.

[8]  W G Tatton,et al.  Contributions of the mesial frontal cortex to the premovement potentials associated with intermittent hand movements in humans , 1996, Human brain mapping.

[9]  S Makeig,et al.  Spatially independent activity patterns in functional MRI data during the stroop color-naming task. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[10]  Baxter P Rogers,et al.  Power spectrum ranked independent component analysis of a periodic fMRI complex motor paradigm , 2003, Human brain mapping.

[11]  James V. Stone Blind Source Separation Using Temporal Predictability , 2001, Neural Computation.

[12]  R. Turner,et al.  Characterizing Evoked Hemodynamics with fMRI , 1995, NeuroImage.

[13]  Markus Svensén,et al.  ICA of fMRI Group Study Data , 2002, NeuroImage.

[14]  G. Curio,et al.  Dipole source localization and fMRI of simultaneously recorded data applied to somatosensory categorization , 2003, NeuroImage.

[15]  J. Hanley,et al.  The meaning and use of the area under a receiver operating characteristic (ROC) curve. , 1982, Radiology.

[16]  R. Freeman,et al.  Single-Neuron Activity and Tissue Oxygenation in the Cerebral Cortex , 2003, Science.

[17]  Dewen Hu,et al.  An Evaluation of Linear Model Analysis Techniques for Processing Images of Microcirculation Activity , 1998, NeuroImage.

[18]  A. Villringer,et al.  No Evidence for Early Decrease in Blood Oxygenation in Rat Whisker Cortex in Response to Functional Activation , 2001, NeuroImage.

[19]  Olivier Faugeras,et al.  Dynamical components analysis of fMRI data through kernel PCA , 2003, NeuroImage.

[20]  Karl J. Friston,et al.  Statistical parametric maps in functional imaging: A general linear approach , 1994 .

[21]  Y. Selen,et al.  Model-order selection: a review of information criterion rules , 2004, IEEE Signal Processing Magazine.

[22]  J. Pekar,et al.  A method for making group inferences from functional MRI data using independent component analysis , 2001, Human brain mapping.

[23]  John E. W. Mayhew,et al.  A Measured Look at Neuronal Oxygen Consumption , 2003, Science.

[24]  S Makeig,et al.  Analysis of fMRI data by blind separation into independent spatial components , 1998, Human brain mapping.

[25]  V D Calhoun,et al.  Spatial and temporal independent component analysis of functional MRI data containing a pair of task‐related waveforms , 2001, Human brain mapping.

[26]  James V. Stone,et al.  Spatiotemporal Independent Component Analysis of Event-Related fMRI Data Using Skewed Probability Density Functions , 2002, NeuroImage.

[27]  M. McKeown Detection of Consistently Task-Related Activations in fMRI Data with Hybrid Independent Component Analysis , 2000, NeuroImage.

[28]  T. Sejnowski,et al.  Single-Trial Variability in Event-Related BOLD Signals , 2002, NeuroImage.

[29]  Riitta Hari,et al.  Activation of human mesial cortex during somatosensory target detection task , 1996, Brain Research.

[30]  R. Turner,et al.  Event-Related fMRI: Characterizing Differential Responses , 1998, NeuroImage.

[31]  R Baumgartner,et al.  Quantification of intensity variations in functional MR images using rotated principal components. , 1996, Physics in medicine and biology.

[32]  E. Oja,et al.  Independent Component Analysis , 2013 .

[33]  I. J. Myung,et al.  When a good fit can be bad , 2002, Trends in Cognitive Sciences.

[34]  Tzyy-Ping Jung,et al.  Imaging brain dynamics using independent component analysis , 2001, Proc. IEEE.

[35]  M. D’Esposito,et al.  Empirical Analyses of BOLD fMRI Statistics , 1997, NeuroImage.

[36]  Karl J. Friston,et al.  Analysis of functional MRI time‐series , 1994, Human Brain Mapping.

[37]  Mark S. Cohen,et al.  Parametric Analysis of fMRI Data Using Linear Systems Methods , 1997, NeuroImage.

[38]  S Makeig,et al.  Blind separation of auditory event-related brain responses into independent components. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[39]  Claus Svarer,et al.  Cluster analysis of activity‐time series in motor learning , 2002, Human brain mapping.

[40]  Wilkin Chau,et al.  An Empirical Comparison of SPM Preprocessing Parameters to the Analysis of fMRI Data , 2002, NeuroImage.

[41]  A. Grinvald,et al.  Non-invasive visualization of cortical columns by fMRI , 2000, Nature Neuroscience.

[42]  V. Mountcastle,et al.  Posterior parietal association cortex of the monkey: command functions for operations within extrapersonal space. , 1975, Journal of neurophysiology.

[43]  Karl J. Friston,et al.  Analysis of fMRI Time-Series Revisited , 1995, NeuroImage.

[44]  V. Haughton,et al.  Whole-brain functional MR imaging activation from a finger-tapping task examined with independent component analysis. , 2000, AJNR. American journal of neuroradiology.

[45]  Motoaki Sugiura,et al.  Brain Activation during the Fist-Edge-Palm Test: A Functional MRI Study , 2002, NeuroImage.

[46]  H. Akaike A new look at the statistical model identification , 1974 .

[47]  Ying Zheng,et al.  Spectroscopic Analysis of Changes in Remitted Illumination: The Response to Increased Neural Activity in Brain , 1999, NeuroImage.

[48]  R. Adler,et al.  The Geometry of Random Fields , 1982 .

[49]  S. Ruan,et al.  A multistep Unsupervised Fuzzy Clustering Analysis of fMRI time series , 2000, Human brain mapping.