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Non-Enhanced T1-Weighted Liver Vessel Imaging at 7 Tesla

OBJECTIVES: Aim of the study was to assess the feasibility and to compare three non-enhanced T1-weighted (w) sequences for liver vessel imaging at 7 Tesla (T). MATERIAL AND METHODS: 12 healthy volunteers were examined on a 7 T whole-body MR-system. The following non-enhanced sequences were acquired:...

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Autores principales: Fischer, Anja, Kraff, Oliver, Maderwald, Stefan, Beiderwellen, Karsten, Ladd, Mark E., Forsting, Michael, Lauenstein, Thomas C., Umutlu, Lale
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4041637/
https://www.ncbi.nlm.nih.gov/pubmed/24887206
http://dx.doi.org/10.1371/journal.pone.0097465
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author Fischer, Anja
Kraff, Oliver
Maderwald, Stefan
Beiderwellen, Karsten
Ladd, Mark E.
Forsting, Michael
Lauenstein, Thomas C.
Umutlu, Lale
author_facet Fischer, Anja
Kraff, Oliver
Maderwald, Stefan
Beiderwellen, Karsten
Ladd, Mark E.
Forsting, Michael
Lauenstein, Thomas C.
Umutlu, Lale
author_sort Fischer, Anja
collection PubMed
description OBJECTIVES: Aim of the study was to assess the feasibility and to compare three non-enhanced T1-weighted (w) sequences for liver vessel imaging at 7 Tesla (T). MATERIAL AND METHODS: 12 healthy volunteers were examined on a 7 T whole-body MR-system. The following non-enhanced sequences were acquired: T1w 2D FLASH, T1w 3D FLASH and Time of flight (TOF)-MRA. Qualitative image analysis was performed by two radiologists including over all image quality as well as vessel delineation of the liver arteries, liver veins and portal vein and the presence of artifacts using a five-point scale (5 = excellent vessel delineation to 1 = non-diagnostic). Contrast ratios (CR), SNR und CNR of the above named vessels in correlation to adjacent liver tissue were calculated for quantitative assessment. For statistical analysis, a Wilcoxon Rank Test was applied. RESULTS: All three sequences provided a homogenous hyperintense delineation of the assessed liver vessels. Qualitative image analysis demonstrated the superiority of TOF-MRA, providing best overall image quality (TOF 4.17, 2D FLASH 3.42, 3D FLASH 3.46; p<0.01) as well as highest image quality values for all analyzed liver vessel segments. TOF-MRA was least impaired by B(1) inhomogeneity (4.13) and susceptibility artifacts (4.63) out of all three sequences (p<0.01). Quantitative image analysis confirmed the superiority of TOF MRA showing significant higher CR values for all liver vessels (e.g. right hepatic artery TOF 0.47, 2D FLASH 0.09, 3D FLASH 0.11 with p = 0.02 and 0.01, respectively). Providing the lowest standard deviation in noise, TOF showed highest values for SNR and CNR. CONCLUSIONS: Non-enhanced T1w imaging in general and TOF MRA in particular, appear to be promising techniques for high quality non-enhanced liver vessel assessment at 7 T.
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spelling pubmed-40416372014-06-09 Non-Enhanced T1-Weighted Liver Vessel Imaging at 7 Tesla Fischer, Anja Kraff, Oliver Maderwald, Stefan Beiderwellen, Karsten Ladd, Mark E. Forsting, Michael Lauenstein, Thomas C. Umutlu, Lale PLoS One Research Article OBJECTIVES: Aim of the study was to assess the feasibility and to compare three non-enhanced T1-weighted (w) sequences for liver vessel imaging at 7 Tesla (T). MATERIAL AND METHODS: 12 healthy volunteers were examined on a 7 T whole-body MR-system. The following non-enhanced sequences were acquired: T1w 2D FLASH, T1w 3D FLASH and Time of flight (TOF)-MRA. Qualitative image analysis was performed by two radiologists including over all image quality as well as vessel delineation of the liver arteries, liver veins and portal vein and the presence of artifacts using a five-point scale (5 = excellent vessel delineation to 1 = non-diagnostic). Contrast ratios (CR), SNR und CNR of the above named vessels in correlation to adjacent liver tissue were calculated for quantitative assessment. For statistical analysis, a Wilcoxon Rank Test was applied. RESULTS: All three sequences provided a homogenous hyperintense delineation of the assessed liver vessels. Qualitative image analysis demonstrated the superiority of TOF-MRA, providing best overall image quality (TOF 4.17, 2D FLASH 3.42, 3D FLASH 3.46; p<0.01) as well as highest image quality values for all analyzed liver vessel segments. TOF-MRA was least impaired by B(1) inhomogeneity (4.13) and susceptibility artifacts (4.63) out of all three sequences (p<0.01). Quantitative image analysis confirmed the superiority of TOF MRA showing significant higher CR values for all liver vessels (e.g. right hepatic artery TOF 0.47, 2D FLASH 0.09, 3D FLASH 0.11 with p = 0.02 and 0.01, respectively). Providing the lowest standard deviation in noise, TOF showed highest values for SNR and CNR. CONCLUSIONS: Non-enhanced T1w imaging in general and TOF MRA in particular, appear to be promising techniques for high quality non-enhanced liver vessel assessment at 7 T. Public Library of Science 2014-06-02 /pmc/articles/PMC4041637/ /pubmed/24887206 http://dx.doi.org/10.1371/journal.pone.0097465 Text en © 2014 Fischer et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Fischer, Anja
Kraff, Oliver
Maderwald, Stefan
Beiderwellen, Karsten
Ladd, Mark E.
Forsting, Michael
Lauenstein, Thomas C.
Umutlu, Lale
Non-Enhanced T1-Weighted Liver Vessel Imaging at 7 Tesla
title Non-Enhanced T1-Weighted Liver Vessel Imaging at 7 Tesla
title_full Non-Enhanced T1-Weighted Liver Vessel Imaging at 7 Tesla
title_fullStr Non-Enhanced T1-Weighted Liver Vessel Imaging at 7 Tesla
title_full_unstemmed Non-Enhanced T1-Weighted Liver Vessel Imaging at 7 Tesla
title_short Non-Enhanced T1-Weighted Liver Vessel Imaging at 7 Tesla
title_sort non-enhanced t1-weighted liver vessel imaging at 7 tesla
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4041637/
https://www.ncbi.nlm.nih.gov/pubmed/24887206
http://dx.doi.org/10.1371/journal.pone.0097465
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