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Individualized arterial spin labeling background suppression by rapid T1 mapping during acquisition

OBJECTIVE: Arterial spin labeling blood perfusion signal relies on the difference between a label and a control image. Background suppression pulses are commonly used to improve the contrast, yet these are based on estimates of tissue relaxation times. The aim of this study is to improve the perfusi...

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Autores principales: Lindner, T., Guerreiro, H., Austein, F., Fiehler, J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9213266/
https://www.ncbi.nlm.nih.gov/pubmed/35118530
http://dx.doi.org/10.1007/s00330-022-08550-8
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author Lindner, T.
Guerreiro, H.
Austein, F.
Fiehler, J.
author_facet Lindner, T.
Guerreiro, H.
Austein, F.
Fiehler, J.
author_sort Lindner, T.
collection PubMed
description OBJECTIVE: Arterial spin labeling blood perfusion signal relies on the difference between a label and a control image. Background suppression pulses are commonly used to improve the contrast, yet these are based on estimates of tissue relaxation times. The aim of this study is to improve the perfusion contrast by individualizing the timing of these background suppression pulses by means of T1 mapping. METHODS: The optimized timing of the background suppression pulses is obtained by rapid T1 mapping employing the variable flip angle technique. Ten healthy volunteers were included in this study. To compare the results, visual grading and the Wilcoxon signed-rank test was used comparing three categories of image quality. RESULTS: The readers confirmed that the images of the proposed method generally show a higher signal-to-background ratio and cortical structures are better visible. Noise was mostly comparable to the standard method. Relative blood flow was statistically significant higher in the modified method. CONCLUSION: The individually optimized background suppression pulses improve the image appearance and allow for a better visualization of cortical structures. The proposed technique however prolongs scan time, which can be seen as negative result, yet needs to be further evaluated. KEY POINTS: • Background suppression timing in ASL can vary. • Both the label and control condition can be modified for T1 mapping. • Adapting the pulse timing improves the signal-to-background ratio.
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spelling pubmed-92132662022-06-23 Individualized arterial spin labeling background suppression by rapid T1 mapping during acquisition Lindner, T. Guerreiro, H. Austein, F. Fiehler, J. Eur Radiol Magnetic Resonance OBJECTIVE: Arterial spin labeling blood perfusion signal relies on the difference between a label and a control image. Background suppression pulses are commonly used to improve the contrast, yet these are based on estimates of tissue relaxation times. The aim of this study is to improve the perfusion contrast by individualizing the timing of these background suppression pulses by means of T1 mapping. METHODS: The optimized timing of the background suppression pulses is obtained by rapid T1 mapping employing the variable flip angle technique. Ten healthy volunteers were included in this study. To compare the results, visual grading and the Wilcoxon signed-rank test was used comparing three categories of image quality. RESULTS: The readers confirmed that the images of the proposed method generally show a higher signal-to-background ratio and cortical structures are better visible. Noise was mostly comparable to the standard method. Relative blood flow was statistically significant higher in the modified method. CONCLUSION: The individually optimized background suppression pulses improve the image appearance and allow for a better visualization of cortical structures. The proposed technique however prolongs scan time, which can be seen as negative result, yet needs to be further evaluated. KEY POINTS: • Background suppression timing in ASL can vary. • Both the label and control condition can be modified for T1 mapping. • Adapting the pulse timing improves the signal-to-background ratio. Springer Berlin Heidelberg 2022-02-04 2022 /pmc/articles/PMC9213266/ /pubmed/35118530 http://dx.doi.org/10.1007/s00330-022-08550-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Magnetic Resonance
Lindner, T.
Guerreiro, H.
Austein, F.
Fiehler, J.
Individualized arterial spin labeling background suppression by rapid T1 mapping during acquisition
title Individualized arterial spin labeling background suppression by rapid T1 mapping during acquisition
title_full Individualized arterial spin labeling background suppression by rapid T1 mapping during acquisition
title_fullStr Individualized arterial spin labeling background suppression by rapid T1 mapping during acquisition
title_full_unstemmed Individualized arterial spin labeling background suppression by rapid T1 mapping during acquisition
title_short Individualized arterial spin labeling background suppression by rapid T1 mapping during acquisition
title_sort individualized arterial spin labeling background suppression by rapid t1 mapping during acquisition
topic Magnetic Resonance
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9213266/
https://www.ncbi.nlm.nih.gov/pubmed/35118530
http://dx.doi.org/10.1007/s00330-022-08550-8
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