Mechanisms underlying decoding at 7 T: ocular dominance columns, broad structures, and macroscopic blood vessels in V1 convey information on the stimulated eye
Open accessAbstract
Recent studies have demonstrated that multivariate machine learning algorithms applied to human functional MRI data can decode information segregated in cortical columns, despite the voxel size being large relative to the width of columns. The mechanism by which low spatial resolution imaging decodes information represented in a fine-scale organization is not clear. To investigate mechanisms underlying decoding signals we employed high-resolution gradient-echo BOLD functional MRI of visual area V1. We show that in addition to the fine-scale ocular dominance columns, coarse-scale structures extending over several millimeters also convey discriminative power for decoding the stimulated eye. Discriminative power is conveyed by both macroscopic blood vessels and gray matter regions. We hypothesize that gray-matter regions which drain into specific vessels may preferentially contain ocular-dominance columns biased towards one eye; the bias of a specific region thereby causing a functionally selective ocular-dominance response in the associated vessel. Our findings indicate that coarse-scale structures and macroscopic blood vessels contribute to decoding of the stimulated eye based on low-resolution multivariate data.
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This smoothing level improves inter-subject functional alignment, while retaining sensitivity to mesoscopic activity patterns that are consistent across individuals.
“This smoothing level improves inter-subject functional alignment, while retaining sensitivity to mesoscopic activity patterns that are consistent across individuals [97].”
From Distinct Brain Systems Mediate the Effects of Nociceptive Input and Self-Regulation on Pain (2015) · cites this paper as [97]
MVPA is more likely to reflect population codes across neurons and has greater sensitivity and specificity to particular types of mental events.
“MVPA is more likely to reflect population codes across neurons43,45,48, as they have demonstrably greater sensitivity and specificity to particular types of mental events17,31,32.”
From Separate neural representations for physical pain and social rejection (2014) · cites this paper as [48]
The smoothing level (8-mm FWHM Gaussian kernel) has been shown to improve inter-subject functional alignment while retaining sensitivity to mesoscopic activity patterns that are consistent across individuals.
“This smoothing level has been shown to improve inter-subject functional alignment, while retaining sensitivity to mesoscopic activity patterns that are consistent across individuals48,66.”
From Separate neural representations for physical pain and social rejection (2014) · cites this paper as [48]
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Cites
Distributed and overlapping representations of faces and objects in ventral temporal cortex
Haxby, J. V., Gobbini, M. I., Furey, M. L., Ishai, A., Schouten, J. L., & Pietrini, P. (2001) · Science · doi:10.1126/science.1063736 · Cited by 3,940 · see citing works
Information-based functional brain mapping
Kriegeskorte, N., Goebel, R., & Bandettini, P. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0600244103 · Cited by 2,113 · see citing works
Decoding the visual and subjective contents of the human brain
Kamitani, Y., & Tong, F. (2005) · Nature Neuroscience · doi:10.1038/nn1444 · Cited by 1,829 · see citing works
Decoding mental states from brain activity in humans
Haynes, J., & Rees, G. E. (2006) · Nature reviews. Neuroscience · doi:10.1038/nrn1931 · Cited by 1,804 · see citing works
Retinotopic organization in human visual cortex and the spatial precision of functional MRI
Engel, S. A. (1997) · Cerebral Cortex · doi:10.1093/cercor/7.2.181 · Cited by 1,606 · see citing works
Predicting the orientation of invisible stimuli from activity in human primary visual cortex
Haynes, J., & Rees, G. E. (2005) · Nature Neuroscience · doi:10.1038/nn1445 · Cited by 866 · see citing works
High-field fMRI unveils orientation columns in humans
Yacoub, E. S., Harel, N., & Uǧurbil, K. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0804110105 · Cited by 564 · see citing works
Self-citationImaging brain function in humans at 7 Tesla
Yacoub, E., Shmuel, A., Pfeuffer, J., Van De Moortele, P., Adriany, G., Andersen, P., Vaughan, J. T., Merkle, H., Ugurbil, K., & Hu, X. (2001) · Magnetic Resonance in Medicine · doi:10.1002/mrm.1080 · Cited by 448 · see citing works
Self-citationMenon, R. S., Ogawa, S., Tank, D. W., & Uǧurbil, K. (1993) · Magnetic Resonance in Medicine · doi:10.1002/mrm.1910300317 · Cited by 412 · see citing works
Human Ocular Dominance Columns as Revealed by High-Field Functional Magnetic Resonance Imaging
Cheng, K., Waggoner, R. A., & Tanaka, K. (2001) · Neuron · doi:10.1016/s0896-6273(01)00477-9 · Cited by 383 · see citing works
An oblique effect in human primary visual cortex
Furmanski, C. S., & Engel, S. A. (2000) · Nature Neuroscience · doi:10.1038/75702 · Cited by 370 · see citing works
Duong, T. Q., Yacoub, E. S., Adriany, G., Hu, X. P., Uǧurbil, K., & Kim, S. (2003) · Magnetic Resonance in Medicine · doi:10.1002/mrm.10472 · Cited by 361 · see citing works
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Kamitani, Y., & Tong, F. (2006) · Current Biology · doi:10.1016/j.cub.2006.04.003 · Cited by 353 · see citing works
Spin‐echo fMRI in humans using high spatial resolutions and high magnetic fields
Yacoub, E. S., Duong, T. Q., de Moortele, P. V., Lindquist, M. A., Adriany, G., Kim, S., Uǧurbil, K., & Hu, X. P. (2003) · Magnetic Resonance in Medicine · doi:10.1002/mrm.10433 · Cited by 308 · see citing works
Self-citationYacoub, E. S., Shmuel, A., Logothetis, N. K., & Uǧurbil, K. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.05.020 · Cited by 305 · see citing works
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Shmuel, A., Yacoub, E., Chaimow, D., Logothetis, N. K., & Ugurbil, K. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2006.12.030 · Cited by 294 · see citing works
Self-citationAgainst hyperacuity in brain reading: Spatial smoothing does not hurt multivariate fMRI analyses?
Op de Beeck, H. P. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2009.02.047 · Cited by 275 · see citing works
Potential pitfalls of functional MRI using conventional gradient‐recalled echo techniques
Kim, S., Hendrich, K. S., Hu, X. P., Merkle, H., & Uǧurbil, K. (1994) · NMR in Biomedicine · doi:10.1002/nbm.1940070111 · Cited by 224 · see citing works
The Radial Bias: A Different Slant on Visual Orientation Sensitivity in Human and Nonhuman Primates
Sasaki, Y., Rajimehr, R., Kim, B. W., Ekstrom, L. B., Vanduffel, W., & Tootell, R. B. H. (2006) · Neuron · doi:10.1016/j.neuron.2006.07.021 · Cited by 195 · see citing works
Quantifying the spatial resolution of the gradient echo and spin echo BOLD response at 3 Tesla
Parkes, L. M., Schwarzbach, J. V., Bouts, A. A., Deckers, R., Pullens, P., Kerskens, C., & Norris, D. G. (2005) · Magnetic Resonance in Medicine · doi:10.1002/mrm.20712 · Cited by 187 · see citing works
Migration and synaptogenesis of cone photoreceptors in the developing mouse retina
Rich, K. A., Zhan, Y., & Blanks, J. C. (1997) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19971110)388:1 · Cited by 156 · see citing works
Brief visual stimulation allows mapping of ocular dominance in visual cortex using fMRI
Goodyear, B. G., & Menon, R. S. (2001) · Human Brain Mapping · doi:10.1002/hbm.1053 · Cited by 142 · see citing works
Arrangement of Ocular Dominance Columns in Human Visual Cortex
Horton, J. C. (1990) · Archives of Ophthalmology · doi:10.1001/archopht.1990.01070090127054 · Cited by 125 · see citing works
The effect of large veins on spatial localization with GE BOLD at 3 T: Displacement, not blurring
Olman, C. A., Inati, S., & Heeger, D. J. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2006.08.045 · Cited by 109 · see citing works
Quantifying the intra‐ and extravascular contributions to spin‐echo fMRI at 3 T
Jochimsen, T. H., Norris, D. G., Mildner, T., & Möller, H. E. (2004) · Magnetic Resonance in Medicine · doi:10.1002/mrm.20221 · Cited by 71 · see citing works
Origin of "decoding" signals in the visual cortex: gray matter or macroscopic blood vessels?
Shmuel, A., Raddatz, G., Chaimow, D., et al. (2007) · MPG.PuRe (Max Planck Society) · Cited by 2 · see citing works
Self-citationChaimow, D., Logothetis, N., Raddatz, G., et al. (2008) · MPG.PuRe (Max Planck Society) · Cited by 1 · see citing works
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Research works printed but not linked: 1
- Gardner JL, Sun P, Tanaka K, Heeger DJ, Cheng K. (2006) Classification analysis with high spatial resolution fMRI reveals large draining veins with orientation specific responses. Proceedings of the Society for Neuroscience meeting, Atlanta.
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Tong, F., & Pratte, M. S. (2012) · Annual Review of Psychology · doi:10.1146/annurev-psych-120710-100412 · Cited by 375 · see citing works
Mathematical framework for large-scale brain network modeling in The Virtual Brain
Sanz-Leon, P., Knock, S. A., Spiegler, A., & Jirsa, V. K. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.01.002 · Cited by 356 · see citing works
Separate neural representations for physical pain and social rejection
Woo, C.-W., Koban, L., Kross, E., Lindquist, M. A., Banich, M. T., Ruzic, L., Andrews-Hanna, J. R., & Wager, T. D. (2014) · Nature Communications · doi:10.1038/ncomms6380 · Cited by 310 · see citing works
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- Authors
- Shmuel, A., Chaimow, D., Raddatz, G., Ugurbil, K., & Yacoub, E.
- Affiliations
- Montreal Neurological Institute and Hospital (CA)
- Max Planck Society (DE)
- University of Minnesota (US)
- Corresponding author
- Shmuel, Amir
- Venue
- NeuroImage
- Publisher
- Elsevier BV
- Published
- 2010-02
- Volume
- 49
- Issue
- 3
- Pages
- 1957-1964
- ISSN
- 1053-8119 (ISSN-L)
- PMC
- PMC8485895
- OpenAlex
- W1980209472
- Cited by
- 111
- References
- 27
- Citations by year
- 2026: 3 · 2025: 3 · 2024: 3 · 2023: 3 · 2022: 7 · 2021: 3 · 2020: 3 · 2019: 5 · 2018: 3 · 2017: 12 · 2016: 8 · 2015: 11 · 2014: 6 · 2013: 4 · 2012: 12
- FWCI
- 5.99
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Locations
- NeuroImage (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Max Planck Institute for Plasma Physics (submittedVersion)
- MPG.PuRe (Max Planck Society) (submittedVersion)
- Funders
- Natural Sciences and Engineering Research Council of Canada
- Canada Research Chairs
- Max-Planck-Gesellschaft
- National Institutes of Health (P30 NS057091, P41 RR08079, R01-EB000331, R01-MH070800)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
- 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
- ocular dominance columns, visual area V1, high-resolution fMRI, multivariate decoding, low spatial resolution
- MeSH terms
- Algorithms, Brain Mapping, Cerebrovascular Circulation, Humans, Image Interpretation, Computer-Assisted, Magnetic Resonance Imaging, Photic Stimulation, Visual Cortex, Visual Pathways, Visual Perception, Dominance, Ocular
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