The DOI matches its Crossref record; 62 of the 64 references it cites were found in a registry or an index.
The impact of global signal regression on resting state correlations: Are anti-correlated networks introduced?
Open accessAbstract
Low-frequency fluctuations in fMRI signal have been used to map several consistent resting state networks in the brain. Using the posterior cingulate cortex as a seed region, functional connectivity analyses have found not only positive correlations in the default mode network but negative correlations in another resting state network related to attentional processes. The interpretation is that the human brain is intrinsically organized into dynamic, anti-correlated functional networks. Global variations of the BOLD signal are often considered nuisance effects and are commonly removed using a general linear model (GLM) technique. This global signal regression method has been shown to introduce negative activation measures in standard fMRI analyses. The topic of this paper is whether such a correction technique could be the cause of anti-correlated resting state networks in functional connectivity analyses. Here we show that, after global signal regression, correlation values to a seed voxel must sum to a negative value. Simulations also show that small phase differences between regions can lead to spurious negative correlation values. A combination breath holding and visual task demonstrates that the relative phase of global and local signals can affect connectivity measures and that, experimentally, global signal regression leads to bell-shaped correlation value distributions, centred on zero. Finally, analyses of negatively correlated networks in resting state data show that global signal regression is most likely the cause of anti-correlations. These results call into question the interpretation of negatively correlated regions in the brain when using global signal regression as an initial processing step.
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“Some physiological noises, such as cardiac and respiratory rates, can alias into the low-frequency domain of functional MRI signals (Strother, 2006;Murphy et al., 2009).”
From Identifying major depression using whole-brain functional connectivity: a multivariate pattern analysis (2012) · cites this paper as Murphy et al., 2009
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“The interpretation of negative correlations is especially controversial because they only become strongly evident after regressing out the global signal; therefore some argue that negative connections in functional data may be purely a statistical artifact (Murphy et al., 2009).”
From Characterizing heterogeneity in children with and without ADHD based on reward system connectivity (2015) · cites this paper as Murphy et al., 2009
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“Some experts have suggested that these techniques might introduce spurious negative correlations upon regressing out whole brain signals (Murphy et al, 2009;Van Dijk et al, 2009).”
From Understanding the Effects of Stimulant Medications on Cognition in Individuals with Attention-Deficit Hyperactivity Disorder: A Decade of Progress (2011) · cites this paper as Murphy et al, 2009
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“Though depression commonly co-occurs with PTSD in veteran populations (up to 80% by some estimations70)”
From Altered resting-state amygdala functional connectivity in men with posttraumatic stress disorder (2012) · cites this paper as [70]
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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
Co-Planar Stereotaxic Atlas of the Human Brain
Talairach, J., & Tournoux, P. (1988) · Medical Entomology and Zoology · Cited by 11,798
AFNI: Software for analysis and visualization of functional magnetic resonance neuroimages
Cox, R. W. (1996) · Computers and Biomedical Research · doi:10.1006/cbmr.1996.0014 · Cited by 10,913
Functional connectivity in the motor cortex of resting human brain using echo‐planar mri
Biswal, B., Zerrin Yetkin, F., Haughton, V. M., & Hyde, J. S. (1995) · Magnetic Resonance in Medicine · doi:10.1002/mrm.1910340409 · Cited by 9,812
The Brain's Default Network: Anatomy, Function, and Relevance to Disease
Buckner, R. L., Andrews‐Hanna, J. R., & Schacter, D. L. (2008) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1440.011 · Cited by 9,761
The human brain is intrinsically organized into dynamic, anticorrelated functional networks
Fox, M. D., Snyder, A. Z., Vincent, J. L., Corbetta, M., Van Essen, D. C., & Raichle, M. E. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0504136102 · Cited by 8,553
Co-planar stereotaxic atlas of the human brain
Laitinen, L. (1989) · Clinical Neurology and Neurosurgery · doi:10.1016/0303-8467(89)90128-5 · Cited by 7,565
Spontaneous fluctuations in brain activity observed with functional magnetic resonance imaging
Fox, M. D., & Raichle, M. E. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2201 · Cited by 6,700
Functional connectivity in the resting brain: a network analysis of the default mode hypothesis
Greicius, M. D., Krasnow, B., Reiss, A. L., & Menon, V. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0135058100 · Cited by 6,358
Consistent resting-state networks across healthy subjects
Damoiseaux, J. S., Rombouts, S. A. R. B., Barkhof, F., Scheltens, P., Stam, C. J., Smith, S. M., & Beckmann, C. F. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0601417103 · Cited by 4,326
Dynamic magnetic resonance imaging of human brain activity during primary sensory stimulation.
Kwong, K. K., Belliveau, J. W., Chesler, D. A., Goldberg, I. E., Weisskoff, R. M., Poncelet, B. P., Kennedy, D. N., Hoppel, B. E., Cohen, M. S., & Turner, R. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.12.5675 · Cited by 4,212
Greicius, M. D., Srivastava, G., Reiss, A. L., & Menon, V. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0308627101 · Cited by 3,684
Wandering minds: the default network and stimulus-independent thought
Mason, M. F., Norton, M. I., Van Horn, J. D., Wegner, D. M., Grafton, S. T., & Macrae, C. N. (2007) · Science · doi:10.1126/science.1131295 · Cited by 2,792
Functional connectivity in single and multislice echoplanar imaging using resting-state fluctuations
Lowe, M. J., Mock, B. J., & Sorenson, J. A. (1998) · NeuroImage · doi:10.1006/nimg.1997.0315 · Cited by 1,394
Fransson, P. (2005) · Human Brain Mapping · doi:10.1002/hbm.20113 · Cited by 1,388
Birn, R. M., Diamond, J. B., Smith, M. A., & Bandettini, P. A. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2006.02.048 · Cited by 1,381
Self-citationCompetition between functional brain networks mediates behavioral variability
Kelly, A. M. C., Uddin, L. Q., Biswal, B. B., Castellanos, F. X., & Milham, M. P. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2007.08.008 · Cited by 1,287
The Variability of Human, BOLD Hemodynamic Responses
Aguirre, G. K., Zarahn, E., & D’Esposito, M. (1998) · NeuroImage · doi:10.1006/nimg.1998.0369 · Cited by 1,251
fMRI resting state networks define distinct modes of long-distance interactions in the human brain
De Luca, M., Beckmann, C. F., De Stefano, N., Matthews, P. M., & Smith, S. M. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2005.08.035 · Cited by 1,241
Aberrant “Default Mode” Functional Connectivity in Schizophrenia
Garrity, A. G., Pearlson, G. D., McKiernan, K., Lloyd, D., Kiehl, K. A., & Calhoun, V. D. (2007) · American Journal of Psychiatry · doi:10.1176/ajp.2007.164.3.450 · Cited by 1,114
Just, M. A., Cherkassky, V. L., Keller, T. A., Kana, R. K., & Minshew, N. J. (2007) · Cerebral Cortex · doi:10.1093/cercor/bhl006 · Cited by 1,081
Handwerker, D. A., Ollinger, J. M., & D’Esposito, M. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2003.11.029 · Cited by 993
Self-citationCoherent spontaneous activity identifies a hippocampal-parietal memory network
Vincent, J. L., Snyder, A. Z., Fox, M. D., Shannon, B. J., Andrews, J. R., Raichle, M. E., & Buckner, R. L. (2006) · Journal of Neurophysiology · doi:10.1152/jn.00048.2006 · Cited by 959 · cited 1×
“This is compatible with the previous suggestion that global signal regression causes correlation strengths to be distributed around zero (Buckner et al., 2008; Vincent et al., 2006), although the equations do not provide any information about the resulting distribution.”
Sonuga-Barke, E. J. S., & Castellanos, F. X. (2007) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2007.02.005 · Cited by 890
The Relationship between Global and Local Changes in PET Scans
Friston, K. J., Frith, C., Liddle, P. F., Dolan, R. J., Lammertsma, A. A., & Frackowiak, R. S. J. (1990) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.1990.88 · Cited by 858
Parametric Analysis of fMRI Data Using Linear Systems Methods
Cohen, M. S. (1997) · NeuroImage · doi:10.1006/nimg.1997.0278 · Cited by 723
Empirical Analyses of BOLD fMRI Statistics
Zarahn, E., Aguirre, G. K., & D’Esposito, M. (1997) · NeuroImage · doi:10.1006/nimg.1997.0263 · Cited by 695
Wise, R. G., Ide, K., Poulin, M. J., & Tracey, I. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2003.11.025 · Cited by 664
Fox, M. D., Snyder, A. Z., Zacks, J. M., & Raichle, M. E. (2006) · Nature Neuroscience · doi:10.1038/nn1616 · Cited by 660
Shmueli, K., van Gelderen, P., de Zwart, J. A., Horovitz, S. G., Fukunaga, M., Jansma, J. M., & Duyn, J. H. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.07.037 · Cited by 546
Failing to deactivate: Resting functional abnormalities in autism
Kennedy, D. P., Redcay, E., & Courchesne, E. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0600674103 · Cited by 543
Fox, P. T., Mintun, M. A., Reiman, E. M., & Raichle, M. E. (1988) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.1988.111 · Cited by 498
Empirical Analyses of BOLD fMRI Statistics
Aguirre, G. K., Zarahn, E., & D’Esposito, M. (1997) · NeuroImage · doi:10.1006/nimg.1997.0264 · Cited by 474
Retrospective estimation and correction of physiological fluctuation in functional MRI
Hu, X. P., Le, T. H., Parrish, T. B., & Erhard, P. (1995) · Magnetic Resonance in Medicine · doi:10.1002/mrm.1910340211 · Cited by 474
Independent component analysis of functional MRI: what is signal and what is noise?
McKeown, M. J., Hansen, L. K., & Sejnowsk, T. J. (2003) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2003.09.012 · Cited by 421
Non-white noise in fMRI: Does modelling have an impact?
Lund, T. E., Madsen, K. H., Sidaros, K., Luo, W., & Nichols, T. E. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2005.07.005 · Cited by 414
A method for removal of global effects from fMRI time series
Macey, P. M., Macey, K. E., Kumar, R., & Harper, R. M. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2003.12.042 · Cited by 407
Independent component analysis of nondeterministic fMRI signal sources
Kiviniemi, V. J., Kantola, J.-H., Jauhiainen, J., Hyvärinen, A., & Tervonen, O. A. (2003) · NeuroImage · doi:10.1016/s1053-8119(03)00097-1 · Cited by 381
Fox, P. T., & Mintun, M. A. (1989) · PubMed · Cited by 335
Top-down modulation of early sensory cortex
Shulman, G. L. (1997) · Cerebral Cortex · doi:10.1093/cercor/7.3.193 · Cited by 328
Birn, R. M., Murphy, K., & Bandettini, P. A. (2008) · Human Brain Mapping · doi:10.1002/hbm.20577 · Cited by 283
Self-citationThe Inferential Impact of Global Signal Covariates in Functional Neuroimaging Analyses
Aguirre, G. K., Zarahn, E., & D’Esposito, M. (1998) · NeuroImage · doi:10.1006/nimg.1998.0367 · Cited by 225
CORSICA: correction of structured noise in fMRI by automatic identification of ICA components
Perlbarg, V., Bellec, P., Anton, J., Pélégrini‐Issac, M., Doyon, J., & Benali, H. (2006) · Magnetic Resonance Imaging · doi:10.1016/j.mri.2006.09.042 · Cited by 201
Data-driven clustering reveals a fundamental subdivision of the human cortex into two global systems
Golland, Y., Golland, P., Bentin, S., & Malach, R. (2008) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2007.10.003 · Cited by 190
Removal of Confounding Effects of Global Signal in Functional MRI Analyses
Desjardins, A. E., Kiehl, K. A., & Liddle, P. F. (2001) · NeuroImage · doi:10.1006/nimg.2000.0719 · Cited by 186
Analysis and use of FMRI response delays
Saad, Z. S., ROPELLA, K. M., Cox, R. W., & DeYoe, E. A. (2001) · Human Brain Mapping · doi:10.1002/hbm.1026 · Cited by 175
Calhoun, V. D., Adali, T., Stevens, M. C., Kiehl, K. A., & Pekar, J. J. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2004.12.012 · Cited by 159
Isolating physiologic noise sources with independently determined spatial measures
Beall, E. B., & Lowe, M. J. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.07.004 · Cited by 157
Default mode network as revealed with multiple methods for resting-state functional MRI analysis
Long, X., Zuo, X., Kiviniemi, V. J., Yang, Y., Zou, Q., Zhu, C.-Z., Jiang, T., Yang, H., Gong, Q., Wang, L. Y., et al. (2008) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2008.03.021 · Cited by 156
Ramsay, S. C., Murphy, K., Shea, S. A., Friston, K. J., Lammertsma, A. A., Clark, J. C., Adams, L. M., Guz, A., & Frackowiak, R. S. J. (1993) · The Journal of Physiology · doi:10.1113/jphysiol.1993.sp019913 · Cited by 133
Self-citationHow to Estimate Global Activity Independent of Changes in Local Activity
Andersson, J. (1997) · NeuroImage · doi:10.1006/nimg.1997.0302 · Cited by 110
Strother, S. C., Anderson, J. R., Schaper, K. A., Sidtis, J. J., Liow, J., Woods, R. P., & Rottenberg, D. A. (1995) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.1995.94 · Cited by 100
Functional MRI of Human Brain during Breath Holding by BOLD and FAIR Techniques
Li, T., Kastrup, A., Takahashi, A., & Moseley, M. E. (1999) · NeuroImage · doi:10.1006/nimg.1998.0399 · Cited by 93
Simulation of the Effects of Global Normalization Procedures in Functional MRI
Gavrilescu, M. C., Shaw, M. E., Stuart, G. W., Eckersley, P., Svalbe, I., & Egan, G. F. (2002) · NeuroImage · doi:10.1006/nimg.2002.1226 · Cited by 78
IMPACT: Image‐based physiological artifacts estimation and correction technique for functional MRI
Chuang, K., & Chen, J. (2001) · Magnetic Resonance in Medicine · doi:10.1002/mrm.1197 · Cited by 72
Junghöfer, M., Schupp, H. T., Stark, R. M., & Vaitl, D. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2004.12.011 · Cited by 70
Arndt, S. V., Cizadlo, T., OʼLeary, D. S., Gold, S. M., & Andreasen, N. C. (1996) · NeuroImage · doi:10.1006/nimg.1996.0019 · Cited by 66
Comparison of methods for detecting nondeterministic BOLD fluctuation in fMRI
Kiviniemi, V. J., Kantola, J.-H., Jauhiainen, J., & Tervonen, O. A. (2004) · Magnetic Resonance Imaging · doi:10.1016/j.mri.2003.09.007 · Cited by 64
A Global Estimator Unbiased by Local Changes
Andersson, J., Ashburner, J., & Friston, K. J. (2001) · NeuroImage · doi:10.1006/nimg.2001.0763 · Cited by 33
Glover (2000) · doi:10.1002/1522-2594(200007)44:1
Flagged first, then by citations
2 of the 64 references couldn’t be matched to a known paper.
Research works printed but not linked: 2
- Fox, M.D., Zhang, D., Snyder, A.Z., Raichle, M.E., 2008. Global signal regression and anticorrelations in resting state fMRI data. Proc. HBM, 575 W-AM.
- Weissenbacher, A., Lanzenberger, R., Moser, E., Windischberger, C., 2008. Increasing specificity of resting-state fMRI-data using multiple regression analysis. Proc. HBM, TH-AM.
Cited by
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The organization of the human cerebellum estimated by intrinsic functional connectivity
Buckner, R. L., Krienen, F. M., Castellanos, A., Diaz, J. C., & Yeo, B. T. T. (2011) · Journal of Neurophysiology · doi:10.1152/jn.00339.2011 · Cited by 7,304
The minimal preprocessing pipelines for the Human Connectome Project
Glasser, M. F., Sotiropoulos, S. N., Wilson, J. A., Coalson, T. S., Fischl, B., Andersson, J. L., Xu, J., Jbabdi, S., Webster, M., Polimeni, J. R., et al. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.04.127 · Cited by 5,253
Conn : A Functional Connectivity Toolbox for Correlated and Anticorrelated Brain Networks
Whitfield-Gabrieli, S., & Nieto-Castanon, A. (2012) · Brain Connectivity · doi:10.1089/brain.2012.0073 · Cited by 4,885
Methods to detect, characterize, and remove motion artifact in resting state fMRI
Power, J. D., Mitra, A., Laumann, T. O., Snyder, A. Z., Schlaggar, B. L., & Petersen, S. E. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2013.08.048 · Cited by 3,748
DPARSF: a MATLAB toolbox for “pipeline” data analysis of resting-state fMRI
Yan (2010) · Frontiers in System Neuroscience · doi:10.3389/fnsys.2010.00013 · Cited by 3,475
Metadata
- Authors
- Murphy, K., Birn, R. M., Handwerker, D. A., Jones, T. B., & Bandettini, P. A.
- Affiliations
- National Institutes of Health (US)
- Corresponding author
- Bandettini, Peter A.
- Venue
- NeuroImage
- Publisher
- Elsevier BV
- Published
- 2009-02
- Volume
- 44
- Issue
- 3
- Pages
- 893-905
- ISSN
- 1053-8119 (ISSN-L)
- PMC
- PMC2750906
- OpenAlex
- W2169787465
- Cited by
- 2,387
- References
- 64
- Citations by year
- 2026: 118 · 2025: 104 · 2024: 109 · 2023: 78 · 2022: 121 · 2021: 133 · 2020: 173 · 2019: 157 · 2018: 166 · 2017: 204 · 2016: 187 · 2015: 188 · 2014: 181 · 2013: 168 · 2012: 114
- FWCI
- 31.87
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- NeuroImage (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health
- National Institute of Mental Health (Z01MH002783)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Functional Brain Connectivity Studies
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Advanced MRI Techniques and Applications
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Advanced Neuroimaging Techniques and Applications
- Keywords
- global signal regression, resting-state functional connectivity, default mode network, attentional networks, posterior cingulate cortex, phase difference, breath-holding, visual task, seed-based correlation analysis
- MeSH terms
- Biological Clocks, Brain, Computer Simulation, Humans, Magnetic Resonance Imaging, Male, Models, Neurological, Nerve Net, Regression Analysis, Rest, Statistics as Topic, Young Adult
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