The Influence of Radio-Frequency Transmit Field Inhomogeneities on the Accuracy of G-ratio Weighted Imaging

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The Influence of Radio-Frequency Transmit Field Inhomogeneities on the Accuracy of G-ratio Weighted Imaging. / Emmenegger, Tim M.; David, Gergely; Ashtarayeh, Mohammad; Fritz, Francisco J.; Ellerbrock, Isabel; Helms, Gunther; Balteau, Evelyne; Freund, Patrick; Mohammadi, Siawoosh.

in: FRONT NEUROSCI-SWITZ, Jahrgang 15, Nr. 1, 674719, 05.07.2021.

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@article{db13c41c7f9a4977aae1a01007f756fd,
title = "The Influence of Radio-Frequency Transmit Field Inhomogeneities on the Accuracy of G-ratio Weighted Imaging",
abstract = "G-ratio weighted imaging is a non-invasive, in-vivo MRI-based technique that aims at estimating an aggregated measure of relative myelination of axons across the entire brain white matter. The MR g-ratio and its constituents (axonal and myelin volume fraction) are more specific to the tissue microstructure than conventional MRI metrics targeting either the myelin or axonal compartment. To calculate the MR g-ratio, an MRI-based myelin-mapping technique is combined with an axon-sensitive MR technique (such as diffusion MRI). Correction for radio-frequency transmit (B1+) field inhomogeneities is crucial for myelin mapping techniques such as magnetization transfer saturation. Here we assessed the effect of B1+ correction on g-ratio weighted imaging. To this end, the B1+ field was measured and the B1+ corrected MR g-ratio was used as the reference in a Bland-Altman analysis. We found a substantial bias (≈-89%) and error (≈37%) relative to the dynamic range of g-ratio values in the white matter if the B1+ correction was not applied. Moreover, we tested the efficiency of a data-driven B1+ correction approach that was applied retrospectively without additional reference measurements. We found that it reduced the bias and error in the MR g-ratio by a factor of three. The data-driven correction is readily available in the open-source hMRI toolbox (www.hmri.info) which is embedded in the statistical parameter mapping (SPM) framework.",
author = "Emmenegger, {Tim M.} and Gergely David and Mohammad Ashtarayeh and Fritz, {Francisco J.} and Isabel Ellerbrock and Gunther Helms and Evelyne Balteau and Patrick Freund and Siawoosh Mohammadi",
note = "Copyright {\textcopyright} 2021 Emmenegger, David, Ashtarayeh, Fritz, Ellerbrock, Helms, Balteau, Freund and Mohammadi.",
year = "2021",
month = jul,
day = "5",
doi = "10.3389/fnins.2021.674719",
language = "English",
volume = "15",
journal = "FRONT NEUROSCI-SWITZ",
issn = "1662-453X",
publisher = "Frontiers Media S. A.",
number = "1",

}

RIS

TY - JOUR

T1 - The Influence of Radio-Frequency Transmit Field Inhomogeneities on the Accuracy of G-ratio Weighted Imaging

AU - Emmenegger, Tim M.

AU - David, Gergely

AU - Ashtarayeh, Mohammad

AU - Fritz, Francisco J.

AU - Ellerbrock, Isabel

AU - Helms, Gunther

AU - Balteau, Evelyne

AU - Freund, Patrick

AU - Mohammadi, Siawoosh

N1 - Copyright © 2021 Emmenegger, David, Ashtarayeh, Fritz, Ellerbrock, Helms, Balteau, Freund and Mohammadi.

PY - 2021/7/5

Y1 - 2021/7/5

N2 - G-ratio weighted imaging is a non-invasive, in-vivo MRI-based technique that aims at estimating an aggregated measure of relative myelination of axons across the entire brain white matter. The MR g-ratio and its constituents (axonal and myelin volume fraction) are more specific to the tissue microstructure than conventional MRI metrics targeting either the myelin or axonal compartment. To calculate the MR g-ratio, an MRI-based myelin-mapping technique is combined with an axon-sensitive MR technique (such as diffusion MRI). Correction for radio-frequency transmit (B1+) field inhomogeneities is crucial for myelin mapping techniques such as magnetization transfer saturation. Here we assessed the effect of B1+ correction on g-ratio weighted imaging. To this end, the B1+ field was measured and the B1+ corrected MR g-ratio was used as the reference in a Bland-Altman analysis. We found a substantial bias (≈-89%) and error (≈37%) relative to the dynamic range of g-ratio values in the white matter if the B1+ correction was not applied. Moreover, we tested the efficiency of a data-driven B1+ correction approach that was applied retrospectively without additional reference measurements. We found that it reduced the bias and error in the MR g-ratio by a factor of three. The data-driven correction is readily available in the open-source hMRI toolbox (www.hmri.info) which is embedded in the statistical parameter mapping (SPM) framework.

AB - G-ratio weighted imaging is a non-invasive, in-vivo MRI-based technique that aims at estimating an aggregated measure of relative myelination of axons across the entire brain white matter. The MR g-ratio and its constituents (axonal and myelin volume fraction) are more specific to the tissue microstructure than conventional MRI metrics targeting either the myelin or axonal compartment. To calculate the MR g-ratio, an MRI-based myelin-mapping technique is combined with an axon-sensitive MR technique (such as diffusion MRI). Correction for radio-frequency transmit (B1+) field inhomogeneities is crucial for myelin mapping techniques such as magnetization transfer saturation. Here we assessed the effect of B1+ correction on g-ratio weighted imaging. To this end, the B1+ field was measured and the B1+ corrected MR g-ratio was used as the reference in a Bland-Altman analysis. We found a substantial bias (≈-89%) and error (≈37%) relative to the dynamic range of g-ratio values in the white matter if the B1+ correction was not applied. Moreover, we tested the efficiency of a data-driven B1+ correction approach that was applied retrospectively without additional reference measurements. We found that it reduced the bias and error in the MR g-ratio by a factor of three. The data-driven correction is readily available in the open-source hMRI toolbox (www.hmri.info) which is embedded in the statistical parameter mapping (SPM) framework.

U2 - 10.3389/fnins.2021.674719

DO - 10.3389/fnins.2021.674719

M3 - SCORING: Journal article

C2 - 34290579

VL - 15

JO - FRONT NEUROSCI-SWITZ

JF - FRONT NEUROSCI-SWITZ

SN - 1662-453X

IS - 1

M1 - 674719

ER -