Evidence map›Paper›PMID 24659952›Full record

ArticleFrontiers in neuroscience2014

BOLD fMRI signal characteristics of S1- and S2-SSFP at 7 Tesla.

Pål E Goa, Peter J Koopmans, Benedikt A Poser, Markus Barth, David G Norris

Abstract read
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Article in Frontiers in neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
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

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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

9 citing papers in PubMed.

  1. Article
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  4. Article
  5. Review
  6. Integrated SSFP for functional brain mapping at 7T with reduced susceptibility artifact.Journal of magnetic resonance (San Diego, Calif. : 1997) · 2017
    Article
  7. Article
  8. Review
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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

5 authors.

Pål E GoaMI-Lab, Department of Medical Imaging, St. Olavs University Hospital Trondheim, Norway ; Erwin L. Hahn Institute of Magnetic Resonance Imaging, University Duisburg-Essen Essen, Germany.
Peter J KoopmansErwin L. Hahn Institute of Magnetic Resonance Imaging, University Duisburg-Essen Essen, Germany ; Centre for Cognitive Neuroimaging, Donders Institute for Brain, Cognition and Behaviour, Radboud University Nijmegen Nijmegen, Netherlands.
Benedikt A PoserErwin L. Hahn Institute of Magnetic Resonance Imaging, University Duisburg-Essen Essen, Germany ; Centre for Cognitive Neuroimaging, Donders Institute for Brain, Cognition and Behaviour, Radboud University Nijmegen Nijmegen, Netherlands.
Markus BarthErwin L. Hahn Institute of Magnetic Resonance Imaging, University Duisburg-Essen Essen, Germany ; Centre for Cognitive Neuroimaging, Donders Institute for Brain, Cognition and Behaviour, Radboud University Nijmegen Nijmegen, Netherlands.
David G NorrisErwin L. Hahn Institute of Magnetic Resonance Imaging, University Duisburg-Essen Essen, Germany ; Centre for Cognitive Neuroimaging, Donders Institute for Brain, Cognition and Behaviour, Radboud University Nijmegen Nijmegen, Netherlands ; MIRA Institute for Biomedical Technology and Technical Medicine, University of Twente Enschede, Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectTo compare the BOLD fMRI signal characteristics at in the cortex and on the pial surface for a non-balanced steady-state free precession sequence (nb-SSFP) at 7 T. MATERIALS AND

methodsA multi-echo nb-SSFP sequence was used for high resolution fMRI at 7 T. Two S1 (S(+)) echoes at different echo times were acquired together with an S2 (S(-)) echo. The primary visual cortex (V1) was examined using a reversing checkerboard paradigm at an isotropic resolution of 0.75 mm, with 35 volumes acquired and a total scan time of 27 min.

resultsSignificant activation was observed in all subjects for all three acquired echoes. For the S1 signal at the longer TE, the activation induced signal change was about 4% in the cortex and 10% at the cortical surface, while for S2 the corresponding values were 3 and 5%.

conclusionFor both S1 and S2 data, the BOLD signal peaks at the pial surface. The large pial surface signal change in S2 may be caused by dynamic averaging around post-capillary vessels embedded within CSF. This is made possible by the long diffusion times of the pathways contributing to the S2 signal and the relatively high diffusion coefficient of CSF. The results indicate that S2-SSFP might not be a suited alternative to spin-echo for high-resolution fMRI at 7 T.

Indexed as

7TBOLDfMRIsteady-state free precessionvisual cortex

Identifiers

PMID24659952
PMCPMC3952481

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