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Improved reproducibility of diffusion MRI of the human brain with a four‐way blip‐up and down phase‐encoding acquisition approach
PURPOSE: To assess the effects of blip‐up and ‐down echo planar imaging (EPI) acquisition designs, with different choices of phase‐encoding directions (PEDs) on the reproducibility of diffusion MRI (dMRI)‐derived metrics in the human brain. METHODS: Diffusion MRI data in seven subjects were acquired...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7898925/ https://www.ncbi.nlm.nih.gov/pubmed/33331068 http://dx.doi.org/10.1002/mrm.28624 |
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author | Irfanoglu, M. Okan Sadeghi, Neda Sarlls, Joelle Pierpaoli, Carlo |
author_facet | Irfanoglu, M. Okan Sadeghi, Neda Sarlls, Joelle Pierpaoli, Carlo |
author_sort | Irfanoglu, M. Okan |
collection | PubMed |
description | PURPOSE: To assess the effects of blip‐up and ‐down echo planar imaging (EPI) acquisition designs, with different choices of phase‐encoding directions (PEDs) on the reproducibility of diffusion MRI (dMRI)‐derived metrics in the human brain. METHODS: Diffusion MRI data in seven subjects were acquired five times, each with five different protocols. The base design included 64 diffusion directions acquired with anterior‐posterior (AP) PED, the first and second protocols added reverse phase‐encoded [Formula: see text] posterior‐anterior (PA) PED images. The third one included 32 directions all with PED acquisitions with opposite polarity (AP and PA). The fourth protocol, also with 32 unique directions used four PEDs (AP, PA, right‐left (RL), and left‐right (LR)). The scan time was virtually identical for all protocols. The variability of diffusion MRI metrics for each subject and each protocol was computed across the different sessions. RESULTS: The highest reproducibility for all dMRI metrics was obtained with protocol four (AP/PA‐RL/LR, ie, four‐way PED). Protocols that used only [Formula: see text] for distortion correction, which are the most widely used designs, had the lowest reproducibility. CONCLUSIONS: An acquisition design with four PEDs, including all DWIs in addition to [Formula: see text] images should be used to achieve high reproducibility in diffusion MRI studies. |
format | Online Article Text |
id | pubmed-7898925 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-78989252021-03-03 Improved reproducibility of diffusion MRI of the human brain with a four‐way blip‐up and down phase‐encoding acquisition approach Irfanoglu, M. Okan Sadeghi, Neda Sarlls, Joelle Pierpaoli, Carlo Magn Reson Med Full Papers—Imaging Methodology PURPOSE: To assess the effects of blip‐up and ‐down echo planar imaging (EPI) acquisition designs, with different choices of phase‐encoding directions (PEDs) on the reproducibility of diffusion MRI (dMRI)‐derived metrics in the human brain. METHODS: Diffusion MRI data in seven subjects were acquired five times, each with five different protocols. The base design included 64 diffusion directions acquired with anterior‐posterior (AP) PED, the first and second protocols added reverse phase‐encoded [Formula: see text] posterior‐anterior (PA) PED images. The third one included 32 directions all with PED acquisitions with opposite polarity (AP and PA). The fourth protocol, also with 32 unique directions used four PEDs (AP, PA, right‐left (RL), and left‐right (LR)). The scan time was virtually identical for all protocols. The variability of diffusion MRI metrics for each subject and each protocol was computed across the different sessions. RESULTS: The highest reproducibility for all dMRI metrics was obtained with protocol four (AP/PA‐RL/LR, ie, four‐way PED). Protocols that used only [Formula: see text] for distortion correction, which are the most widely used designs, had the lowest reproducibility. CONCLUSIONS: An acquisition design with four PEDs, including all DWIs in addition to [Formula: see text] images should be used to achieve high reproducibility in diffusion MRI studies. John Wiley and Sons Inc. 2020-12-16 2021-05 /pmc/articles/PMC7898925/ /pubmed/33331068 http://dx.doi.org/10.1002/mrm.28624 Text en Published 2020. This article is a U.S. Government work and is in the public domain in the USA. Magnetic Resonance in Medicine published by Wiley Periodicals LLC 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-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Full Papers—Imaging Methodology Irfanoglu, M. Okan Sadeghi, Neda Sarlls, Joelle Pierpaoli, Carlo Improved reproducibility of diffusion MRI of the human brain with a four‐way blip‐up and down phase‐encoding acquisition approach |
title | Improved reproducibility of diffusion MRI of the human brain with a four‐way blip‐up and down phase‐encoding acquisition approach |
title_full | Improved reproducibility of diffusion MRI of the human brain with a four‐way blip‐up and down phase‐encoding acquisition approach |
title_fullStr | Improved reproducibility of diffusion MRI of the human brain with a four‐way blip‐up and down phase‐encoding acquisition approach |
title_full_unstemmed | Improved reproducibility of diffusion MRI of the human brain with a four‐way blip‐up and down phase‐encoding acquisition approach |
title_short | Improved reproducibility of diffusion MRI of the human brain with a four‐way blip‐up and down phase‐encoding acquisition approach |
title_sort | improved reproducibility of diffusion mri of the human brain with a four‐way blip‐up and down phase‐encoding acquisition approach |
topic | Full Papers—Imaging Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7898925/ https://www.ncbi.nlm.nih.gov/pubmed/33331068 http://dx.doi.org/10.1002/mrm.28624 |
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