Evidence map›Paper›PMID 28461461›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2017

High spatial correspondence at a columnar level between activation and resting state fMRI signals and local field potentials.

Zhaoyue Shi, Ruiqi Wu, Pai-Feng Yang, Feng Wang, Tung-Lin Wu, Arabinda Mishra, Li Min Chen, John C Gore

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.8field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

26 citing papers in PubMed, 40 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Zhaoyue ShiDepartment of Biomedical Engineering, Vanderbilt University, Nashville, TN 37235; zhaoyue.shi@vanderbilt.edu.
Ruiqi WuVanderbilt University Institute of Imaging Science, Vanderbilt University, Nashville, TN 37235.
Pai-Feng YangVanderbilt University Institute of Imaging Science, Vanderbilt University, Nashville, TN 37235.
Feng WangVanderbilt University Institute of Imaging Science, Vanderbilt University, Nashville, TN 37235.
Tung-Lin WuDepartment of Biomedical Engineering, Vanderbilt University, Nashville, TN 37235.
Arabinda MishraVanderbilt University Institute of Imaging Science, Vanderbilt University, Nashville, TN 37235.
Li Min ChenVanderbilt University Institute of Imaging Science, Vanderbilt University, Nashville, TN 37235.
John C GoreDepartment of Biomedical Engineering, Vanderbilt University, Nashville, TN 37235.
Vanderbilt University · US

Funding

Biophysical Basis of Functional Connectivity by MRIR01NS078680 · NINDS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Li Min Chen, John C Gore · 2012 to 2026
$7.6M
Research Project: Sensory and Multisensory Contributions to AutismU54HD083211 · NICHD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI DYKENS, ELISABETH MAY · 2015 to 2019
$7.1M
Representation of Nociception in SII and Thalamus of PrimatesR01NS069909 · NINDS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI CHEN, LI MIN · 2012 to 2016
$1.7M
CONTRAST MECHANISMS IN DIFFUSION WEIGHTED MRI OF BRAINR01NS034834 · NINDS · YALE UNIVERSITY · PI GORE, JOHN C · 1996 to 2008
$1.4M
NICHD NIH HHS U54 HD083211NINDS NIH HHS R01 NS034834NINDS NIH HHS R01 NS069909NINDS NIH HHS R01 NS078680
6 · The paper itself

Abstract

Although blood oxygenation level-dependent (BOLD) fMRI has been widely used to map brain responses to external stimuli and to delineate functional circuits at rest, the extent to which BOLD signals correlate spatially with underlying neuronal activity, the spatial relationships between stimulus-evoked BOLD activations and local correlations of BOLD signals in a resting state, and whether these spatial relationships vary across functionally distinct cortical areas are not known. To address these critical questions, we directly compared the spatial extents of stimulated activations and the local profiles of intervoxel resting state correlations for both high-resolution BOLD at 9.4 T and local field potentials (LFPs), using 98-channel microelectrode arrays, in functionally distinct primary somatosensory areas 3b and 1 in nonhuman primates. Anatomic images of LFP and BOLD were coregistered within 0.10 mm accuracy. We found that the point spread functions (PSFs) of BOLD and LFP responses were comparable in the stimulus condition, and both estimates of activations were slightly more spatially constrained than local correlations at rest. The magnitudes of stimulus responses in area 3b were stronger than those in area 1 and extended in a medial to lateral direction. In addition, the reproducibility and stability of stimulus-evoked activation locations within and across both modalities were robust. Our work suggests that the intrinsic resolution of BOLD is not a limiting feature in practice and approaches the intrinsic precision achievable by multielectrode electrophysiology.

Indexed as

AnimalsBrainBrain MappingImage Processing, Computer-AssistedMagnetic Resonance ImagingNeuronsNeurovascular CouplingReproducibility of ResultsRestSaimiriSomatosensory CortexBOLD fMRIlocal field potentialpoint spread functionprimary somatosensory cortexresting state correlations

Identifiers

PMID28461461
PMCPMC5441782
OpenAlexW2610173433

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.