Semi-blind ICA of fMRI: a method for utilizing hypothesis-derived time courses in a spatial ICA analysis
Abstract
Independent component analysis (ICA) is a data-driven approach utilizing high-order statistical moments to find maximally independent sources that has found fruitful application in functional magnetic resonance imaging (fMRI). Being a blind source separation technique, ICA does not require any explicit constraints upon the fMRI time courses. However, for some fMRI data analysis applications, such as for the analysis of an event-related paradigm, it would be useful to flexibly incorporate paradigm information into the ICA analysis. In this paper, we present an approach for constrained or semi-blind ICA (sbICA) analysis of event-related fMRI data by imposing regularization on certain estimated time courses using the paradigm information. We demonstrate the performance of our approach using both simulations and fMRI data from a three-stimulus auditory oddball paradigm. Simulation results suggest that (1) a regression approach slightly outperforms ICA when prior information is accurate and ICA outperforms the general linear model (GLM)-based approach when prior information is not completely accurate, (2) prior information improves the robustness of ICA in the presence of noise, and (3) ICA analysis using prior information with temporal constraints can outperform a regression approach when the prior information is not completely accurate. Using fMRI data, we compare a regression-based conjunction analysis of target and novel stimuli, both of which elicit an orienting response, to an sbICA approach utilizing both the target and novel stimuli to constrain the ICA time courses. Results show similar positive associations for both GLM and sbICA, but sbICA detects additional negative associates consistent with regions implicated in a default mode of brain activity. This suggests that task-related default mode decreases have a more "complex" signal that benefits from a flexible modeling approach. Compared with a traditional GLM approach, the sbICA approach provides a flexible way to analyze fMRI data that reduces the assumptions placed upon the hemodynamic response of the brain. The advantages and limitations of our technique are discussed in detail in the manuscript to provide guidelines to the reader for developing useful applications. The use of prior time course information in a spatial ICA analysis, which combines elements of both a regression approach and a blind ICA approach, may prove to be a useful tool for fMRI analysis.
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Only trials in which the participant responded correctly were modeled, and this had only a small quantitative impact on the reported findings.
“In order to further reduce within scan variability in neural activity, only trials in which the participant responded correctly (hit and correct rejection) were modeled, with onset time-locked to the beginning of each trial (Calhoun et al., 2005; Demir et al., 2014; Hammer et al., 2015; Puschmann et al., 2013). This had only a small quantitative impact on the reported findings.”
From Functional neuroimaging of visuospatial working memory tasks enables accurate detection of attention deficit and hyperactivity disorder (2015) · cites this paper as Calhoun et al., 2005
Cites
A default mode of brain function
Raichle, M. E., MacLeod, A. M., Snyder, A. Z., Powers, W. J., Gusnard, D. A., & Shulman, G. L. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.98.2.676 · Cited by 12,190 · see citing works
An Information-Maximization Approach to Blind Separation and Blind Deconvolution
Bell, A. J., & Sejnowski, T. J. (1995) · Neural Computation · doi:10.1162/neco.1995.7.6.1129 · Cited by 8,986 · see citing works
Thresholding of statistical maps in functional neuroimaging using the false discovery rate
Genovese, C. R., Lazar, N. A., & Nichols, T. (2002) · NeuroImage · doi:10.1006/nimg.2001.1037 · Cited by 4,923 · see citing works
Spatial registration and normalization of images
Friston, K. J., Ashburner, J., Frith, C., Poline, J.-B., Heather, J. D., & Frackowiak, R. S. J. (1995) · Human Brain Mapping · doi:10.1002/hbm.460030303 · Cited by 3,744 · see citing works
A method for making group inferences from functional MRI data using independent component analysis
Calhoun, V. D., Adali, T., Pearlson, G. D., & Pekar, J. J. (2001) · Human Brain Mapping · doi:10.1002/hbm.1048 · Cited by 2,994 · see citing works
Self-citationAnalysis of fMRI Time-Series Revisited
Friston, K. J., Holmes, A. P., Poline, J., Grasby, P. M., Williams, S., Frackowiak, R. S. J., & Turner, R. (1995) · NeuroImage · doi:10.1006/nimg.1995.1007 · Cited by 2,504 · see citing works
Analysis of fMRI Time-Series Revisited—Again
Worsley, K. J., & Friston, K. J. (1995) · NeuroImage · doi:10.1006/nimg.1995.1023 · Cited by 2,198 · see citing works
A New Learning Algorithm for Blind Signal Separation
Амари, Ш.-И., Cichocki, A. S., & Yang, H. H. (1995) · Cited by 1,904 · see citing works
Cognitive Conjunction: A New Approach to Brain Activation Experiments
Price, C. J., & Friston, K. J. (1997) · NeuroImage · doi:10.1006/nimg.1997.0269 · Cited by 839 · see citing works
Calhoun, V. D., Adalı, T., Pearlson, G. D., & Pekar, J. J. (2001) · Human Brain Mapping · doi:10.1002/hbm.1024 · Cited by 697 · see citing works
Self-citationInfomax and maximum likelihood for blind source separation
Cardoso, J.-F. (1997) · IEEE Signal Processing Letters · doi:10.1109/97.566704 · Cited by 681 · see citing works
Kiehl, K. A., Laurens, K. R., Duty, T., Forster, B. B., & Liddle, P. F. (2001) · Psychophysiology · doi:10.1111/1469-8986.3810133 · Cited by 397 · see citing works
Self-citationWhat is the best similarity measure for motion correction in fMRI time series?
Freire, L., Roche, A., & Mangin, J. (2002) · IEEE Transactions on Medical Imaging · doi:10.1109/tmi.2002.1009383 · Cited by 353 · see citing works
Calhoun, V. D., Adalı, T., McGinty, V. B., Pekar, J. J., Watson, T. D., & Pearlson, G. D. (2001) · NeuroImage · doi:10.1006/nimg.2001.0921 · Cited by 305 · see citing works
Self-citationMotion Correction Algorithms May Create Spurious Brain Activations in the Absence of Subject Motion
Freire, L., & Mangin, J. (2001) · NeuroImage · doi:10.1006/nimg.2001.0869 · Cited by 305 · see citing works
Different activation dynamics in multiple neural systems during simulated driving
Calhoun, V. D., Pekar, J. J., McGinty, V. B., Adalı, T., Watson, T. D., & Pearlson, G. D. (2002) · Human Brain Mapping · doi:10.1002/hbm.10032 · Cited by 274 · see citing works
Self-citationBiswal, B. B., & Ulmer, J. L. (1999) · Journal of Computer Assisted Tomography · doi:10.1097/00004728-199903000-00016 · Cited by 255 · see citing works
Event-related fMRI of auditory and visual oddball tasks
Stevens, A. A., Skudlarski, P., Gatenby, J. C., & Gore, J. C. (2000) · Magnetic Resonance Imaging · doi:10.1016/s0730-725x(00)00128-4 · Cited by 234 · see citing works
Single-Trial Variability in Event-Related BOLD Signals
Duann, J., Jung, T., Kuo, W., Yeh, T., Makeig, S., Hsieh, J., & B, T. J. S. A. (2002) · NeuroImage · doi:10.1006/nimg.2001.1049 · Cited by 215 · see citing works
Spatiotemporal Pattern of Neural Processing in the Human Auditory Cortex
Seifritz, E., Esposito, F., Hennel, F., Mustovic, H., Neuhoff, J. G., Bilecen, D., Tedeschi, G., Scheffler, K., & Salle, F. D. (2002) · Science · doi:10.1126/science.1074355 · Cited by 213 · see citing works
Kiehl, K. A., & Liddle, P. F. (2001) · Schizophrenia Research · doi:10.1016/s0920-9964(00)00117-1 · Cited by 213 · see citing works
Self-citationCalhoun, V. D., Stevens, M. C. G., Pearlson, G. D., & Kiehl, K. A. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2003.12.029 · Cited by 210 · see citing works
Self-citationStone, J. V., Porrill, J., Porter, N. R., & Wilkinson, I. D. (2002) · NeuroImage · doi:10.1006/nimg.2001.0986 · Cited by 182 · see citing works
McKeown, M. J. (2000) · NeuroImage · doi:10.1006/nimg.1999.0518 · Cited by 175 · see citing works
Svensén, M., Kruggel, F., & Benali, H. (2002) · NeuroImage · doi:10.1006/nimg.2002.1122 · Cited by 134 · see citing works
A Bayesian approach to source separationPreprint
Knuth, K. H. (2002) · arXiv (Cornell University) · doi:10.48550/arxiv.physics/0205032 · Cited by 104 · see citing works
Calhoun, V. D., Adalı, T., Pekar, J. J., & Pearlson, G. D. (2003) · NeuroImage · doi:10.1016/s1053-8119(03)00411-7 · Cited by 83 · see citing works
Self-citationIndependent Component Analysis Applied to fMRI Data: A Generative Model for Validating Results
Calhoun, V. D., Pearlson, G. D., & Adali, T. (2004) · The Journal of VLSI Signal Processing Systems for Signal Image and Video Technology · doi:10.1023/b:vlsi.0000027491.81326.7a · Cited by 74 · see citing works
Self-citationDifferent activation dynamics in multiple neural systems during simulated driving
Calhoun, V. D., Pekar, J. J., McGinty, V. B., Adalı, T., Watson, T. D., & Pearlson, G. D. (2002) · Human Brain Mapping · doi:10.1002/hbm.10066 · Cited by 60 · see citing works
Self-citationMultivariate Bayesian Statistics
Rowe, D. B. (2002) · Chapman & Hall/CRC eBooks · doi:10.1201/9781420035261 · Cited by 58 · see citing works
Eliminating indeterminacy in ICA
Lu, W., & Rajapakse, J. C. (2003) · Neurocomputing · doi:10.1016/s0925-2312(01)00710-x · Cited by 51 · see citing works
Suzuki, K., Kiryu, T., & Nakada, T. (2001) · Human Brain Mapping · doi:10.1002/hbm.1061 · Cited by 51 · see citing works
GROUP ICA OF FUNCTIONAL MRI DATA: SEPARABILITY, STATIONARITY, AND INFERENCE
Calhoun, V. D., Adalı, T., Pearlson, G. D., & Pekar, J. J. (2001) · Cited by 48 · see citing works
Self-citationHabituation and sensitization of the orienting response following bilateral anterior cingulotomy
Cohen, R. A., Kaplan, R. F., Meadows, M., & Wilkinson, H. A. (1994) · Neuropsychologia · doi:10.1016/0028-3932(94)90148-1 · Cited by 46 · see citing works
Nakada, T., Suzuki, K., Fujii, Y., Matsuzawa, H., & Kwee, I. L. (2000) · Neuroscience Research · doi:10.1016/s0168-0102(00)00122-x · Cited by 34 · see citing works
Sparse imaging of the auditory oddball task with functional MRI
Müller, B. W., Stude, P., Nebel, K., Wiese, H., Ladd, M. E., Forsting, M., & Jueptner, M. (2003) · Neuroreport · doi:10.1097/00001756-200308260-00011 · Cited by 31 · see citing works
Flexible Bayesian Independent Component Analysis for Blind Source Separation
Choudrey, R., & Roberts, S. J. (2001) · Cited by 28 · see citing works
Exploratory motion analysis in fMRI using ICA
Bannister, P. R., Beckmann, C. F., & Jenkinson, M. (2001) · NeuroImage · doi:10.1016/s1053-8119(01)91412-0 · Cited by 6 · see citing works
Flagged first, then by citations
Cited by
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Murphy, K., Birn, R. M., Handwerker, D. A., Jones, T. B., & Bandettini, P. A. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2008.09.036 · Cited by 2,387 · see citing works
Network homogeneity reveals decreased integrity of default-mode network in ADHD
Uddin, L. Q., Kelly, A. M. C., Biswal, B. B., Margulies, D. S., Shehzad, Z., Shaw, D., Ghaffari, M., Rotrosen, J., Adler, L. A., Castellanos, F. X., et al. (2008) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2007.11.031 · Cited by 452 · see citing works
Čeko, M., Shir, Y., Ouellet, J. A., Ware, M. A., Stone, L. S., & Seminowicz, D. A. (2015) · Human Brain Mapping · doi:10.1002/hbm.22757 · Cited by 171 · see citing works
Sensory-motor brain network connectivity for speech comprehension
Londei, A., D'Ausilio, A., Basso, D., Sestieri, C., Gratta, C. D., Romani, G., & Belardinelli, M. O. (2010) · Human Brain Mapping · doi:10.1002/hbm.20888 · Cited by 90 · see citing works
Hammer, R., Cooke, G. E., Stein, M. A., & Booth, J. R. (2015) · NeuroImage: Clinical · doi:10.1016/j.nicl.2015.08.015 · Cited by 25 · see citing works
Hammer, R., Tennekoon, M., Cooke, G. E., Gayda, J., Stein, M. A., & Booth, J. R. (2015) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2015.06.002 · Cited by 21 · see citing works
- Authors
- Calhoun, V. D., Adali, T., Stevens, M. C., Kiehl, K. A., & Pekar, J. J.
- Affiliations
- Johns Hopkins University (US)
- Yale University (US)
- Kennedy Krieger Institute (US)
- Corresponding author
- Calhoun, V.D.
- Venue
- NeuroImage
- Publisher
- Elsevier BV
- Published
- 2005-04
- Volume
- 25
- Issue
- 2
- Pages
- 527-538
- ISSN
- 1053-8119 (ISSN-L)
- OpenAlex
- W2064464200
- Cited by
- 159
- References
- 39
- Citations by year
- 2025: 6 · 2024: 5 · 2023: 3 · 2022: 3 · 2021: 5 · 2020: 3 · 2019: 6 · 2018: 4 · 2017: 13 · 2016: 7 · 2015: 8 · 2014: 10 · 2013: 13 · 2012: 8
- FWCI
- 15.29
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- NeuroImage (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health
- National Institute of Biomedical Imaging and Bioengineering (R01EB000840)
- Topics
- Physical Sciences › Computer Science › Signal Processing › Blind Source Separation Techniques
- Life Sciences › Neuroscience › Cognitive Neuroscience › Functional Brain Connectivity Studies
- Physical Sciences › Mathematics › Computational Mathematics › Tensor decomposition and applications
- Keywords
- independent component analysis, functional MRI, event-related fMRI, auditory oddball paradigm, regularization, default mode network, hemodynamic response, conjunction analysis, orienting response
- MeSH terms
- Auditory Perception, Brain, Humans, Magnetic Resonance Imaging, Time, Principal Component Analysis
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