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Gradient‐echo and spin‐echo blood oxygenation level–dependent functional MRI at ultrahigh fields of 9.4 and 15.2 Tesla

PURPOSE: Sensitivity and specificity of blood oxygenation level–dependent (BOLD) functional MRI (fMRI) is sensitive to magnetic field strength and acquisition methods. We have investigated gradient‐echo (GE)‐ and spin‐echo (SE)‐BOLD fMRI at ultrahigh fields of 9.4 and 15.2  Tesla. METHODS: BOLD fMRI...

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Autores principales: Han, SoHyun, Son, Jeong Pyo, Cho, HyungJoon, Park, Jang‐Yeon, Kim, Seong‐Gi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6585650/
https://www.ncbi.nlm.nih.gov/pubmed/30183108
http://dx.doi.org/10.1002/mrm.27457
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author Han, SoHyun
Son, Jeong Pyo
Cho, HyungJoon
Park, Jang‐Yeon
Kim, Seong‐Gi
author_facet Han, SoHyun
Son, Jeong Pyo
Cho, HyungJoon
Park, Jang‐Yeon
Kim, Seong‐Gi
author_sort Han, SoHyun
collection PubMed
description PURPOSE: Sensitivity and specificity of blood oxygenation level–dependent (BOLD) functional MRI (fMRI) is sensitive to magnetic field strength and acquisition methods. We have investigated gradient‐echo (GE)‐ and spin‐echo (SE)‐BOLD fMRI at ultrahigh fields of 9.4 and 15.2  Tesla. METHODS: BOLD fMRI experiments responding to forepaw stimulation were performed with 3 echo times (TE) at each echo type and B (0) in α‐chloralose–anesthetized rats. The contralateral forelimb somatosensory region was selected for quantitative analyses. RESULTS: At 9.4 T and 15.2 T, average baseline T (2) (*) (n = 9) was 26.6 and 17.1 msec, whereas baseline T (2 )value (n = 9) was 35.7 and 24.5 msec, respectively. Averaged stimulation‐induced ΔR (2) (*) was –1.72 s(–1) at 9.4 T and –3.09 s(–1) at 15.2 T, whereas ΔR (2) was –1.19 s(–1) at 9.4 T and –1.97 s(–1) at 15.2 T. At the optimal TE of tissue T (2) (*) or T (2), BOLD percent changes were slightly higher at 15.2 T than at 9.4 T (GE: 7.4% versus 6.4% and SE: 5.7% versus 5.4%). The ΔR (2) (*) and ΔR (2) ratio of 15.2 T to 9.4 T was 1.8 and 1.66, respectively. The ratio of the macrovessel‐containing superficial to microvessel‐dominant parenchymal BOLD signal was 1.73 to 1.76 for GE‐BOLD versus 1.13 to 1.19 for SE‐BOLD, indicating that the SE‐BOLD contrast is less sensitive to macrovessels than GE‐BOLD. CONCLUSION: SE‐BOLD fMRI improves spatial specificity to microvessels compared to GE‐BOLD at both fields. BOLD sensitivity is similar at the both fields and can be improved at ultrahigh fields only for thermal‐noise–dominant ultrahigh‐resolution fMRI.
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spelling pubmed-65856502019-06-27 Gradient‐echo and spin‐echo blood oxygenation level–dependent functional MRI at ultrahigh fields of 9.4 and 15.2 Tesla Han, SoHyun Son, Jeong Pyo Cho, HyungJoon Park, Jang‐Yeon Kim, Seong‐Gi Magn Reson Med Full Papers—Biophysics and Basic Biomedical Research PURPOSE: Sensitivity and specificity of blood oxygenation level–dependent (BOLD) functional MRI (fMRI) is sensitive to magnetic field strength and acquisition methods. We have investigated gradient‐echo (GE)‐ and spin‐echo (SE)‐BOLD fMRI at ultrahigh fields of 9.4 and 15.2  Tesla. METHODS: BOLD fMRI experiments responding to forepaw stimulation were performed with 3 echo times (TE) at each echo type and B (0) in α‐chloralose–anesthetized rats. The contralateral forelimb somatosensory region was selected for quantitative analyses. RESULTS: At 9.4 T and 15.2 T, average baseline T (2) (*) (n = 9) was 26.6 and 17.1 msec, whereas baseline T (2 )value (n = 9) was 35.7 and 24.5 msec, respectively. Averaged stimulation‐induced ΔR (2) (*) was –1.72 s(–1) at 9.4 T and –3.09 s(–1) at 15.2 T, whereas ΔR (2) was –1.19 s(–1) at 9.4 T and –1.97 s(–1) at 15.2 T. At the optimal TE of tissue T (2) (*) or T (2), BOLD percent changes were slightly higher at 15.2 T than at 9.4 T (GE: 7.4% versus 6.4% and SE: 5.7% versus 5.4%). The ΔR (2) (*) and ΔR (2) ratio of 15.2 T to 9.4 T was 1.8 and 1.66, respectively. The ratio of the macrovessel‐containing superficial to microvessel‐dominant parenchymal BOLD signal was 1.73 to 1.76 for GE‐BOLD versus 1.13 to 1.19 for SE‐BOLD, indicating that the SE‐BOLD contrast is less sensitive to macrovessels than GE‐BOLD. CONCLUSION: SE‐BOLD fMRI improves spatial specificity to microvessels compared to GE‐BOLD at both fields. BOLD sensitivity is similar at the both fields and can be improved at ultrahigh fields only for thermal‐noise–dominant ultrahigh‐resolution fMRI. John Wiley and Sons Inc. 2018-09-05 2019-02 /pmc/articles/PMC6585650/ /pubmed/30183108 http://dx.doi.org/10.1002/mrm.27457 Text en © 2019 The Authors. Magnetic Resonance in Medicine published by Wiley Periodicals, Inc. on behalf of International Society for Magnetic Resonance in Medicine This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Full Papers—Biophysics and Basic Biomedical Research
Han, SoHyun
Son, Jeong Pyo
Cho, HyungJoon
Park, Jang‐Yeon
Kim, Seong‐Gi
Gradient‐echo and spin‐echo blood oxygenation level–dependent functional MRI at ultrahigh fields of 9.4 and 15.2 Tesla
title Gradient‐echo and spin‐echo blood oxygenation level–dependent functional MRI at ultrahigh fields of 9.4 and 15.2 Tesla
title_full Gradient‐echo and spin‐echo blood oxygenation level–dependent functional MRI at ultrahigh fields of 9.4 and 15.2 Tesla
title_fullStr Gradient‐echo and spin‐echo blood oxygenation level–dependent functional MRI at ultrahigh fields of 9.4 and 15.2 Tesla
title_full_unstemmed Gradient‐echo and spin‐echo blood oxygenation level–dependent functional MRI at ultrahigh fields of 9.4 and 15.2 Tesla
title_short Gradient‐echo and spin‐echo blood oxygenation level–dependent functional MRI at ultrahigh fields of 9.4 and 15.2 Tesla
title_sort gradient‐echo and spin‐echo blood oxygenation level–dependent functional mri at ultrahigh fields of 9.4 and 15.2 tesla
topic Full Papers—Biophysics and Basic Biomedical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6585650/
https://www.ncbi.nlm.nih.gov/pubmed/30183108
http://dx.doi.org/10.1002/mrm.27457
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