Cited by 684Functional Brain Connectivity StudiesMind wandering and attentionNeural dynamics and brain function

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Default-Mode Activity during a Passive Sensory Task: Uncoupled from Deactivation but Impacting Activation

Greicius, Michael D., Menon, Vinod·2004·Journal of Cognitive Neuroscience

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Abstract

Deactivation refers to increased neural activity during low-demand tasks or rest compared with high-demand tasks. Several groups have reported that a particular set of brain regions, including the posterior cingulate cortex and the medial prefrontal cortex, among others, is consistently deactivated. Taken together, these typically deactivated brain regions appear to constitute a default-mode network of brain activity that predominates in the absence of a demanding external task. Examining a passive, block-design sensory task with a standard deactivation analysis (rest epochs vs. stimulus epochs), we demonstrate that the default-mode network is undetectable in one run and only partially detectable in a second run. Using independent component analysis, however, we were able to detect the full default-mode network in both runs and to demonstrate that, in the majority of subjects, it persisted across both rest and stimulus epochs, uncoupled from the task waveform, and so mostly undetectable as deactivation. We also replicate an earlier finding that the default-mode network includes the hippocampus suggesting that episodic memory is incorporated in default-mode cognitive processing. Furthermore, we show that the more a subject's default-mode activity was correlated with the rest epochs (and “deactivated” during stimulus epochs), the greater that subject's activation to the visual and auditory stimuli. We conclude that activity in the default-mode network may persist through both experimental and rest epochs if the experiment is not sufficiently challenging. Time-series analysis of default-mode activity provides a measure of the degree to which a task engages a subject and whether it is sufficient to interrupt the processes—presumably cognitive, internally generated, and involving episodic memory—mediated by the default-mode network.

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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
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
Self-citation
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
Default-mode network activity distinguishes Alzheimer’s disease from healthy aging: evidence from functional MRI
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
Self-citation
Searching for a baseline: Functional imaging and the resting human brain
Gusnard, D. A., & Raichle, M. E. (2001) · Nature Reviews Neuroscience · doi:10.1038/35094500 · Cited by 3,371
Medial prefrontal cortex and self-referential mental activity: Relation to a default mode of brain function
Gusnard, D. A., Akbudak, E., Shulman, G. L., & Raichle, M. E. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.071043098 · Cited by 2,997
Probabilistic Independent Component Analysis for Functional Magnetic Resonance Imaging
Beckmann, C. F., & Smith, S. M. (2004) · IEEE Transactions on Medical Imaging · doi:10.1109/tmi.2003.822821 · Cited by 2,707
Common blood flow changes across visual tasks: II. Decreases in cerebral cortex
Shulman, G. L., Fiez, J. A., Corbetta, M., Buckner, R. L., Miezin, F. M., Raichle, M. E., & Petersen, S. E. (1997) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.1997.9.5.648 · Cited by 1,890
Intersubject synchronization of cortical activity during natural vision
Hasson, U., Nir, Y., Levy, I., Fuhrmann, G., & Malach, R. (2004) · Science · doi:10.1126/science.1089506 · Cited by 1,839
Frequencies contributing to functional connectivity in the cerebral cortex in "resting-state" data.
Cordes, D., Haughton, V. M., Arfanakis, K., Carew, J. D., Turski, P. A., Moritz, C. H., Quigley, M., & Meyerand, M. E. (2001) · PubMed Central · Cited by 1,402

Show all 28 references

Research works printed but not linked: 3

Cordes D., 2001, AJNR American Journal of Neuroradiology, 22, 1326
McGuire P. K., 1996, NeuroReport, 7, 2095
Quigley M. A., 2002, AJNR American Journal of Neuroradiology, 23, 49

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Hansen, N. L., Lauritzen, M., Mortensen, E. L., Osler, M., Avlund, K., Fagerlund, B., & Rostrup, E. (2014) · Human Brain Mapping · doi:10.1002/hbm.22489 · Cited by 48
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Chen, Y., Yang, W., Long, J., Zhang, Y., Feng, J., Li, Y., & Huang, B. (2015) · PLoS ONE · doi:10.1371/journal.pone.0124153 · Cited by 50
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Meltzer, J. A., Negishi, M., & Constable, R. T. (2007) · Human Brain Mapping · doi:10.1002/hbm.20391 · Cited by 48
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Authors: Greicius, M. D., & Menon, V.
Affiliations: Stanford Medicine (US)
ORCID: Greicius, Michael D.
Menon, Vinod
Venue: Journal of Cognitive Neuroscience
Publisher: MIT Press - Journals
Published: 2004-11-01
Volume: 16
Issue: 9
Pages: 1484-1492
ISSN: 0898-929X (ISSN-L)
1530-8898
DOI: 10.1162/0898929042568532
OpenAlex: W2069444194
Cited by: 684
References: 28
Citations by year: 2026: 4 · 2025: 3 · 2024: 21 · 2023: 10 · 2022: 18 · 2021: 31 · 2020: 27 · 2019: 33 · 2018: 21 · 2017: 42 · 2016: 45 · 2015: 40 · 2014: 42 · 2013: 54 · 2012: 46
FWCI: 12.16
Type: journal article
Language: en
Open access: closed
Locations: Journal of Cognitive Neuroscience (publishedVersion)
PubMed (publishedVersion)
Funders: Eunice Kennedy Shriver National Institute of Child Health and Human Development (K25HD040761, HD40761)
Topics: Life Sciences › Neuroscience › Cognitive Neuroscience › Functional Brain Connectivity Studies
Life Sciences › Neuroscience › Cognitive Neuroscience › Mind wandering and attention
Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
Keywords: default mode network, deactivation, posterior cingulate cortex, medial prefrontal cortex, hippocampus, episodic memory, task engagement, independent component analysis, resting-state brain activity
MeSH terms: Arousal, Auditory Cortex, Brain, Brain Mapping, Electrophysiology, Factor Analysis, Statistical, Hippocampus, Humans, Magnetic Resonance Imaging, Mental Processes, Models, Neurological, Neural Inhibition, Neural Pathways, Perception, Reference Values, Rest, Sensation, Sensory Thresholds, Signal Processing, Computer-Assisted, Visual Cortex, Principal Component Analysis

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Default-Mode Activity during a Passive Sensory Task: Uncoupled from Deactivation but Impacting Activation

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