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A Parametric Manipulation of Factors Affecting Task-induced Deactivation in Functional Neuroimaging
Abstract
Task-induced deactivation (TID) refers to a regional decrease in blood flow during an active task relative to a “resting” or “passive” baseline. We tested the hypothesis that TID results from a reallocation of processing resources by parametrically manipulating task difficulty within three factors: target discriminability, stimulus presentation rate, and short-term memory load. Subjects performed an auditory target detection task during functional magnetic resonance imaging (fMRI), responding to a single target tone or, in the short-term memory load conditions, to target sequences. Seven task conditions (a common version and two additional levels for each of the three factors) were each alternated with “rest” in a block design. Analysis of covariance identified brain regions in which TID occurred. Analyses of variance identified seven regions (left anterior cingulate/superior frontal gyrus, left middle frontal gyrus, right anterior cingulate gyrus, left and right posterior cingulate gyrus, left posterior parieto-occipital cortex, and right precuneus) in which TID magnitude varied across task levels within a factor. Follow-up tests indicated that for each of the three factors, TID magnitude increased with task difficulty. These results suggest that TID represents reallocation of processing resources from areas in which TID occurs to areas involved in task performance. Short-term memory load and stimulus rate also predict suppression of spontaneous thought, and many of the brain areas showing TID have been linked with semantic processing, supporting claims that TID may be due in part to suspension of spontaneous semantic processes that occur during “rest” (Binder et al., 1999). The concept that the typical “resting state” is actually a condition characterized by rich cognitive activity has important implications for the design and analysis of neuroimaging studies.
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“Furthermore, these drivers may suppress off-task and self-focused attention, buffering learners from these obstacles to optimal performance (McKiernan, Kaufman, Kucera-Thompson, & Binder, 2003).”
From Optimizing performance through intrinsic motivation and attention for learning: The OPTIMAL theory of motor learning (2016) · cites this paper as McKiernan, Kaufman, Kucera-Thompson, & Binder, 2003
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Cites
The assessment and analysis of handedness: The Edinburgh inventory
Oldfield, R. C. (1971) · Neuropsychologia · doi:10.1016/0028-3932(71)90067-4 · Cited by 35,900
James, W. (1891) · Personality Culture Society · doi:10.1037/11059-000 · Cited by 25,876
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
Brain magnetic resonance imaging with contrast dependent on blood oxygenation.
Ogawa, S., Lee, T. M., Kay, A. R., & Tank, D. W. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.24.9868 · Cited by 6,483
Beaton, A. E., & Keppel, G. (1975) · American Educational Research Journal · doi:10.2307/1162588 · Cited by 5,857
Imaging Cognition II: An Empirical Review of 275 PET and fMRI Studies
Cabeza, R., & Nyberg, L. (2000) · Journal of Cognitive Neuroscience · doi:10.1162/08989290051137585 · Cited by 3,598
Emotion, Decision Making and the Orbitofrontal Cortex
Bechara, A. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.3.295 · Cited by 3,589
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
Research works printed but not linked: 3
- 10.2466/pms.1966.23.2.399 · DOI · Paper page
- Ingvar D. H., 1985, Human Neurobiology, 4, 127
- McGuire P. K., 1996, NeuroReport, 7, 2095
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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
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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
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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
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Spreng, R. N., Mar, R. A., & Kim, A. S. N. (2009) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2008.21029 · Cited by 2,143
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Uddin, L. Q., Clare Kelly, A. M., Biswal, B. B., Xavier Castellanos, F., & Milham, M. P. (2009) · Human Brain Mapping · doi:10.1002/hbm.20531 · Cited by 1,135
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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
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Pizzagalli, D. A. (2011) · Neuropsychopharmacology · doi:10.1038/npp.2010.166 · Cited by 945
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Utevsky, A. V., Smith, D. V., & Huettel, S. A. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.4227-13.2014 · Cited by 925
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Lustig, C., Snyder, A. Z., Bhakta, M., O'Brien, K. C., McAvoy, M., Raichle, M. E., Morris, J. C., & Buckner, R. L. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2235925100 · Cited by 720
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Fukunaga, M., Horovitz, S. G., van Gelderen, P., de Zwart, J. A., Jansma, J. M., Ikonomidou, V. N., Chu, R., Deckers, R. H. R., Leopold, D. A., & Duyn, J. H. (2006) · Magnetic Resonance Imaging · doi:10.1016/j.mri.2006.04.018 · Cited by 375
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Northoff, G., Walter, M., Schulte, R. F., Beck, J., Dydak, U., Henning, A., Boeker, H., Grimm, S., & Boesiger, P. (2007) · Nature Neuroscience · doi:10.1038/nn2001 · Cited by 359
Grimm, S., Boesiger, P., Beck, J., Schuepbach, D., Bermpohl, F., Walter, M., Ernst, J., Hell, D., Boeker, H., & Northoff, G. (2009) · Neuropsychopharmacology · doi:10.1038/npp.2008.81 · Cited by 350
Spreng, R. N., Wojtowicz, M. A., & Grady, C. L. (2010) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2010.01.009 · Cited by 383
Golland, Y., Bentin, S., Gelbard, H., Benjamini, Y., Heller, R., Nir, Y., Hasson, U., & Malach, R. (2007) · Cerebral Cortex · doi:10.1093/cercor/bhk030 · Cited by 337
Grady, C. L., Sarraf, S., Saverino, C., & Campbell, K. L. (2016) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2016.02.020 · Cited by 357
Calhoun, V. D., Maciejewski, P. K., Pearlson, G. D., & Kiehl, K. A. (2007) · Human Brain Mapping · doi:10.1002/hbm.20463 · Cited by 351
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Satpute, A. B., & Lieberman, M. D. (2006) · Brain Research · doi:10.1016/j.brainres.2006.01.005 · Cited by 347
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Binder, J. R., McKiernan, K. A., Parsons, M. E., Westbury, C. F., Possing, E. T., Kaufman, J. N., & Buchanan, L. (2003) · Journal of Cognitive Neuroscience · doi:10.1162/089892903321593108 · Cited by 344
Self-citationSadaghiani, S., Hesselmann, G., & Kleinschmidt, A. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.2592-09.2009 · Cited by 325
Grady, C. L., Protzner, A. B., Kovacevic, N., Strother, S. C., Afshin‐Pour, B., Wojtowicz, M., Anderson, J. A. E., Churchill, N. W., & McIntosh, A. R. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhp207 · Cited by 352
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Singh, K. D., & Fawcett, I. P. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.01.051 · Cited by 312
Bush, G., & Shin, L. M. (2006) · Nature Protocols · doi:10.1038/nprot.2006.48 · Cited by 309
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Minzenberg, M., Fan, J., New, A. S., Tang, C. Y., & Siever, L. J. (2007) · Psychiatry Research Neuroimaging · doi:10.1016/j.pscychresns.2007.03.006 · Cited by 314
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Martin, U., Keller, J., Hoenig, K., Waller, C., & Grön, G. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.08.019 · Cited by 352
Age Differences in Deactivation: A Link to Cognitive Control?
Persson, J., Lustig, C., Nelson, J. K., & Reuter‐Lorenz, P. A. (2007) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2007.19.6.1021 · Cited by 329
Reading normal and degraded words: Contribution of the dorsal and ventral visual pathways.
Cohen, L., Dehaene, S., Vinckier, F., Jobert, A., & Montavont, A. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2007.11.036 · Cited by 303
Multiple neuronal networks mediate sustained attention
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Metadata
- Authors
- McKiernan, K. A., Kaufman, J. N., Kucera-Thompson, J., & Binder, J. R.
- Affiliations
- Medical College of Wisconsin (US)
- Venue
- Journal of Cognitive Neuroscience
- Publisher
- MIT Press
- Published
- 2003-04-01
- Volume
- 15
- Issue
- 3
- Pages
- 394-408
- ISSN
- 0898-929X (ISSN-L)
- 1530-8898
- OpenAlex
- W2169605136
- Cited by
- 1,080
- References
- 56
- Citations by year
- 2026: 12 · 2025: 15 · 2024: 19 · 2023: 20 · 2022: 29 · 2021: 41 · 2020: 42 · 2019: 47 · 2018: 33 · 2017: 39 · 2016: 62 · 2015: 44 · 2014: 77 · 2013: 82 · 2012: 76
- FWCI
- 14.96
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Cognitive Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute of Mental Health (P01MH051358, P0 MH51358)
- National Institute of Neurological Disorders and Stroke (R01NS033576)
- National Center for Research Resources (M01RR000058)
- 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 and Behavioral Psychology Studies
- Keywords
- task-induced deactivation, resting state, task difficulty, stimulus presentation rate, auditory target detection, posterior cingulate cortex, precuneus, anterior cingulate cortex, semantic processing
- MeSH terms
- Acoustic Stimulation, Adult, Auditory Perception, Brain, Brain Mapping, Cerebrovascular Circulation, Female, Humans, Magnetic Resonance Imaging, Male, Memory, Short-Term, Mental Processes, Middle Aged
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