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Cerebrospinal fluid–suppressed T(2)‐weighted MR imaging at 7 T for human brain

PURPOSE: T(2)‐weighted lesional imaging is most commonly performed using inversion recovery turbo spin echoes. At 7 T, however, this acquisition is limited for specific absorption rate and resolution. This work describes and implements a method to generate CSF‐suppressed T(2)‐weighted imaging. METHO...

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Autores principales: Pan, Jullie W., Moon, Chan Hong, Hetherington, Hoby P.
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/PMC6590483/
https://www.ncbi.nlm.nih.gov/pubmed/30450583
http://dx.doi.org/10.1002/mrm.27598
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author Pan, Jullie W.
Moon, Chan Hong
Hetherington, Hoby P.
author_facet Pan, Jullie W.
Moon, Chan Hong
Hetherington, Hoby P.
author_sort Pan, Jullie W.
collection PubMed
description PURPOSE: T(2)‐weighted lesional imaging is most commonly performed using inversion recovery turbo spin echoes. At 7 T, however, this acquisition is limited for specific absorption rate and resolution. This work describes and implements a method to generate CSF‐suppressed T(2)‐weighted imaging. METHODS: The strategy uses a driven equilibrium spin‐echo preparation within an inversion recovery with multiple 3D gradient‐echo imaging blocks. Images are combined using the self‐normalization approach, which achieves CSF suppression through optimized timing of individual blocks and minimizes sources of variation due to coil receptivity, T(2) (*), and proton density. Simulations of the magnetization‐prepared fluid‐attenuated inversion recovery gradient‐echo (MPFLAGRE) method over T(1) and T(2) relaxation values are performed, and in vivo demonstrations using an 8 [Formula: see text] 2 transceiver array in healthy controls are shown. RESULTS: The specific absorption rate of the calculated MPFLAGRE sequence is 11.1 ± 0.5 W (n = 5 volunteers), which is 74 ± 2% of the US Food and Drug Administration guidelines. This method acquires both contrasts for CSF suppression with detection of long T(2) components and T(2)‐weighted imaging in a single acquisition. In healthy controls, the former contrast generates increased signal in the cortical rim and ependyma. A comparison is shown with a conventional 3D SPACE fluid‐attenuated inversion recovery acquisition, and sensitivity to pathology is demonstrated in an epilepsy patient. CONCLUSION: As applied with the 8 [Formula: see text] 2 transceiver, the MPFLAGRE sequence generates both whole‐brain contrast suitable for lesional and T(2)‐weighted imaging at 7 T in fewer than 10 minutes within the US Food and Drug Administration's specific absorption rate guidelines.
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spelling pubmed-65904832019-07-08 Cerebrospinal fluid–suppressed T(2)‐weighted MR imaging at 7 T for human brain Pan, Jullie W. Moon, Chan Hong Hetherington, Hoby P. Magn Reson Med Full Papers—Imaging Methodology PURPOSE: T(2)‐weighted lesional imaging is most commonly performed using inversion recovery turbo spin echoes. At 7 T, however, this acquisition is limited for specific absorption rate and resolution. This work describes and implements a method to generate CSF‐suppressed T(2)‐weighted imaging. METHODS: The strategy uses a driven equilibrium spin‐echo preparation within an inversion recovery with multiple 3D gradient‐echo imaging blocks. Images are combined using the self‐normalization approach, which achieves CSF suppression through optimized timing of individual blocks and minimizes sources of variation due to coil receptivity, T(2) (*), and proton density. Simulations of the magnetization‐prepared fluid‐attenuated inversion recovery gradient‐echo (MPFLAGRE) method over T(1) and T(2) relaxation values are performed, and in vivo demonstrations using an 8 [Formula: see text] 2 transceiver array in healthy controls are shown. RESULTS: The specific absorption rate of the calculated MPFLAGRE sequence is 11.1 ± 0.5 W (n = 5 volunteers), which is 74 ± 2% of the US Food and Drug Administration guidelines. This method acquires both contrasts for CSF suppression with detection of long T(2) components and T(2)‐weighted imaging in a single acquisition. In healthy controls, the former contrast generates increased signal in the cortical rim and ependyma. A comparison is shown with a conventional 3D SPACE fluid‐attenuated inversion recovery acquisition, and sensitivity to pathology is demonstrated in an epilepsy patient. CONCLUSION: As applied with the 8 [Formula: see text] 2 transceiver, the MPFLAGRE sequence generates both whole‐brain contrast suitable for lesional and T(2)‐weighted imaging at 7 T in fewer than 10 minutes within the US Food and Drug Administration's specific absorption rate guidelines. John Wiley and Sons Inc. 2018-11-19 2019-05 /pmc/articles/PMC6590483/ /pubmed/30450583 http://dx.doi.org/10.1002/mrm.27598 Text en © 2018 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—Imaging Methodology
Pan, Jullie W.
Moon, Chan Hong
Hetherington, Hoby P.
Cerebrospinal fluid–suppressed T(2)‐weighted MR imaging at 7 T for human brain
title Cerebrospinal fluid–suppressed T(2)‐weighted MR imaging at 7 T for human brain
title_full Cerebrospinal fluid–suppressed T(2)‐weighted MR imaging at 7 T for human brain
title_fullStr Cerebrospinal fluid–suppressed T(2)‐weighted MR imaging at 7 T for human brain
title_full_unstemmed Cerebrospinal fluid–suppressed T(2)‐weighted MR imaging at 7 T for human brain
title_short Cerebrospinal fluid–suppressed T(2)‐weighted MR imaging at 7 T for human brain
title_sort cerebrospinal fluid–suppressed t(2)‐weighted mr imaging at 7 t for human brain
topic Full Papers—Imaging Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6590483/
https://www.ncbi.nlm.nih.gov/pubmed/30450583
http://dx.doi.org/10.1002/mrm.27598
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