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A Parametric Manipulation of Factors Affecting Task-induced Deactivation in Functional Neuroimaging

McKiernan, Kristen A., Kaufman, Jacqueline N., Kucera-Thompson, Jane, Binder, Jeffrey R.·2003·Journal of Cognitive Neuroscience

DOI 10.1162/089892903321593117

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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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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
The Principles of Psychology
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
Book Reviews: Keppel, Geoffrey. Design and Analysis: A Researcher’s Handbook . Englewood Cliffs, N. J.: Prentice Hall, 1973. 658 + xiii pp. $13.95
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

Show all 56 references

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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Authors: McKiernan, K. A., Kaufman, J. N., Kucera-Thompson, J., & Binder, J. R.
Affiliations: Medical College of Wisconsin (US)
ORCID: Kaufman, Jacqueline N.
Binder, Jeffrey R.
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
DOI: 10.1162/089892903321593117
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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A Parametric Manipulation of Factors Affecting Task-induced Deactivation in Functional Neuroimaging

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