TY - JOUR
T1 - Robust high spatio-temporal line-scanning fMRI in humans at 7T using multi-echo readouts, denoising and prospective motion correction
AU - Raimondo, Luisa
AU - Priovoulos, Nikos
AU - Passarinho, Catarina
AU - Heij, Jurjen
AU - Knapen, Tomas
AU - Dumoulin, Serge O.
AU - Siero, Jeroen C.W.
AU - van der Zwaag, Wietske
N1 - Funding Information:
This work was supported by Royal Netherlands Acadamy for Arts and Sciences (KNAW) research grant (2018, to S.O.D., W.Z, J.S.), a Netherlands Organization for Scientific Research (NWO) Vidi Grant (TTW VI.Vidi.198.016 to W.Z.), an NWO Vici (016.Vici.185.050 to S.O.D.) and an Ammodo KNAW Award (S.O.D.).
Publisher Copyright:
© 2022 The Authors
Copyright © 2022 The Authors. Published by Elsevier B.V. All rights reserved.
PY - 2023/1/15
Y1 - 2023/1/15
N2 - Background: Functional magnetic resonance imaging (fMRI), typically using blood oxygenation level-dependent (BOLD) contrast weighted imaging, allows the study of brain function with millimeter spatial resolution and temporal resolution of one to a few seconds. At a mesoscopic scale, neurons in the human brain are spatially organized in structures with dimensions of hundreds of micrometers, while they communicate at the millisecond timescale. For this reason, it is important to develop an fMRI method with simultaneous high spatial and temporal resolution. Line-scanning promises to reach this goal at the cost of volume coverage. New method: Here, we release a comprehensive update to human line-scanning fMRI. First, we investigated multi-echo line-scanning with five different protocols varying the number of echoes and readout bandwidth while keeping the TR constant. In these, we compared different echo combination approaches in terms of BOLD activation (sensitivity) and temporal signal-to-noise ratio. Second, we implemented an adaptation of NOise reduction with DIstribution Corrected principal component analysis (NORDIC) thermal noise removal for line-scanning fMRI data. Finally, we tested three image-based navigators for motion correction and investigated different ways of performing fMRI analysis on the timecourses which were influenced by the insertion of the navigators themselves. Results: The presented improvements are relatively straightforward to implement; multi-echo readout and NORDIC denoising together, significantly improve data quality in terms of tSNR and t-statistical values, while motion correction makes line-scanning fMRI more robust. Comparison with existing methods: Multi-echo acquisitions and denoising have previously been applied in 3D magnetic resonance imaging. Their combination and application to 1D line-scanning is novel. The current proposed method greatly outperforms the previous line-scanning acquisitions with single-echo acquisition, in terms of tSNR (4.0 for single-echo line-scanning and 36.2 for NORDIC-denoised multi-echo) and t-statistical values (3.8 for single-echo line-scanning and 25.1 for NORDIC-denoised multi-echo line-scanning). Conclusions: Line-scanning fMRI was advanced compared to its previous implementation in order to improve sensitivity and reliability. The improved line-scanning acquisition could be used, in the future, for neuroscientific and clinical applications.
AB - Background: Functional magnetic resonance imaging (fMRI), typically using blood oxygenation level-dependent (BOLD) contrast weighted imaging, allows the study of brain function with millimeter spatial resolution and temporal resolution of one to a few seconds. At a mesoscopic scale, neurons in the human brain are spatially organized in structures with dimensions of hundreds of micrometers, while they communicate at the millisecond timescale. For this reason, it is important to develop an fMRI method with simultaneous high spatial and temporal resolution. Line-scanning promises to reach this goal at the cost of volume coverage. New method: Here, we release a comprehensive update to human line-scanning fMRI. First, we investigated multi-echo line-scanning with five different protocols varying the number of echoes and readout bandwidth while keeping the TR constant. In these, we compared different echo combination approaches in terms of BOLD activation (sensitivity) and temporal signal-to-noise ratio. Second, we implemented an adaptation of NOise reduction with DIstribution Corrected principal component analysis (NORDIC) thermal noise removal for line-scanning fMRI data. Finally, we tested three image-based navigators for motion correction and investigated different ways of performing fMRI analysis on the timecourses which were influenced by the insertion of the navigators themselves. Results: The presented improvements are relatively straightforward to implement; multi-echo readout and NORDIC denoising together, significantly improve data quality in terms of tSNR and t-statistical values, while motion correction makes line-scanning fMRI more robust. Comparison with existing methods: Multi-echo acquisitions and denoising have previously been applied in 3D magnetic resonance imaging. Their combination and application to 1D line-scanning is novel. The current proposed method greatly outperforms the previous line-scanning acquisitions with single-echo acquisition, in terms of tSNR (4.0 for single-echo line-scanning and 36.2 for NORDIC-denoised multi-echo) and t-statistical values (3.8 for single-echo line-scanning and 25.1 for NORDIC-denoised multi-echo line-scanning). Conclusions: Line-scanning fMRI was advanced compared to its previous implementation in order to improve sensitivity and reliability. The improved line-scanning acquisition could be used, in the future, for neuroscientific and clinical applications.
KW - 7T
KW - BOLD fMRI
KW - Denoising
KW - Line-scanning
KW - Motion correction
KW - Multi-echo
KW - Reproducibility of Results
KW - Prospective Studies
KW - Echo-Planar Imaging/methods
KW - Brain Mapping/methods
KW - Humans
KW - Magnetic Resonance Imaging/methods
KW - Brain/diagnostic imaging
UR - http://www.scopus.com/inward/record.url?scp=85142704362&partnerID=8YFLogxK
U2 - 10.1016/j.jneumeth.2022.109746
DO - 10.1016/j.jneumeth.2022.109746
M3 - Article
C2 - 36403778
AN - SCOPUS:85142704362
SN - 0165-0270
VL - 384
SP - 1
EP - 12
JO - Journal of Neuroscience Methods
JF - Journal of Neuroscience Methods
M1 - 109746
ER -