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In Vivo Magic Angle Magnetic Resonance Imaging for Cell Tracking in Equine Low-Field MRI

The magic angle effect increases the MRI signal of healthy tendon tissue and could be used for more detailed evaluation of tendon structure. Furthermore, it could support the discrimination of hypointense artefacts induced by contrast agents such as superparamagnetic iron oxide used for cell trackin...

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Autores principales: Horstmeier, Carolin, Ahrberg, Annette B., Berner, Dagmar, Burk, Janina, Gittel, Claudia, Hillmann, Aline, Offhaus, Julia, Brehm, Walter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6942896/
https://www.ncbi.nlm.nih.gov/pubmed/31933650
http://dx.doi.org/10.1155/2019/5670106
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author Horstmeier, Carolin
Ahrberg, Annette B.
Berner, Dagmar
Burk, Janina
Gittel, Claudia
Hillmann, Aline
Offhaus, Julia
Brehm, Walter
author_facet Horstmeier, Carolin
Ahrberg, Annette B.
Berner, Dagmar
Burk, Janina
Gittel, Claudia
Hillmann, Aline
Offhaus, Julia
Brehm, Walter
author_sort Horstmeier, Carolin
collection PubMed
description The magic angle effect increases the MRI signal of healthy tendon tissue and could be used for more detailed evaluation of tendon structure. Furthermore, it could support the discrimination of hypointense artefacts induced by contrast agents such as superparamagnetic iron oxide used for cell tracking. However, magic angle MRI of the equine superficial digital flexor tendon has not been accomplished in vivo in standing low-field MRI so far. The aim of this in vivo study was to evaluate the practicability of this magic angle technique and its benefit for tracking superparamagnetic iron oxide-labelled multipotent mesenchymal stromal cells. Six horses with induced tendinopathy in their forelimb superficial digital flexor tendons were injected locally either with superparamagnetic iron oxide-labelled multipotent mesenchymal stromal cells or serum. MRI included standard and magic angle image series in T1- and T2∗-weighted sequences performed at regular intervals. Image analysis comprised blinded evaluation and quantitative assessment of signal-to-noise ratio. The magic angle technique enhanced the tendon signal-to-noise ratio (P < 0.001). Hypointense artefacts were observable in the cell-injected superficial digital flexor tendons over 24 weeks and artefact signal-to-noise ratio differed significantly from tendon signal-to-noise ratio in the magic angle images (P < 0.001). Magic angle imaging of the equine superficial digital flexor tendon is feasible in standing low-field MRI. The current data demonstrate that the technique improves discrimination of superparamagnetic iron oxide-induced artefacts from the surrounding tendon tissue.
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spelling pubmed-69428962020-01-13 In Vivo Magic Angle Magnetic Resonance Imaging for Cell Tracking in Equine Low-Field MRI Horstmeier, Carolin Ahrberg, Annette B. Berner, Dagmar Burk, Janina Gittel, Claudia Hillmann, Aline Offhaus, Julia Brehm, Walter Stem Cells Int Research Article The magic angle effect increases the MRI signal of healthy tendon tissue and could be used for more detailed evaluation of tendon structure. Furthermore, it could support the discrimination of hypointense artefacts induced by contrast agents such as superparamagnetic iron oxide used for cell tracking. However, magic angle MRI of the equine superficial digital flexor tendon has not been accomplished in vivo in standing low-field MRI so far. The aim of this in vivo study was to evaluate the practicability of this magic angle technique and its benefit for tracking superparamagnetic iron oxide-labelled multipotent mesenchymal stromal cells. Six horses with induced tendinopathy in their forelimb superficial digital flexor tendons were injected locally either with superparamagnetic iron oxide-labelled multipotent mesenchymal stromal cells or serum. MRI included standard and magic angle image series in T1- and T2∗-weighted sequences performed at regular intervals. Image analysis comprised blinded evaluation and quantitative assessment of signal-to-noise ratio. The magic angle technique enhanced the tendon signal-to-noise ratio (P < 0.001). Hypointense artefacts were observable in the cell-injected superficial digital flexor tendons over 24 weeks and artefact signal-to-noise ratio differed significantly from tendon signal-to-noise ratio in the magic angle images (P < 0.001). Magic angle imaging of the equine superficial digital flexor tendon is feasible in standing low-field MRI. The current data demonstrate that the technique improves discrimination of superparamagnetic iron oxide-induced artefacts from the surrounding tendon tissue. Hindawi 2019-12-17 /pmc/articles/PMC6942896/ /pubmed/31933650 http://dx.doi.org/10.1155/2019/5670106 Text en Copyright © 2019 Carolin Horstmeier et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Horstmeier, Carolin
Ahrberg, Annette B.
Berner, Dagmar
Burk, Janina
Gittel, Claudia
Hillmann, Aline
Offhaus, Julia
Brehm, Walter
In Vivo Magic Angle Magnetic Resonance Imaging for Cell Tracking in Equine Low-Field MRI
title In Vivo Magic Angle Magnetic Resonance Imaging for Cell Tracking in Equine Low-Field MRI
title_full In Vivo Magic Angle Magnetic Resonance Imaging for Cell Tracking in Equine Low-Field MRI
title_fullStr In Vivo Magic Angle Magnetic Resonance Imaging for Cell Tracking in Equine Low-Field MRI
title_full_unstemmed In Vivo Magic Angle Magnetic Resonance Imaging for Cell Tracking in Equine Low-Field MRI
title_short In Vivo Magic Angle Magnetic Resonance Imaging for Cell Tracking in Equine Low-Field MRI
title_sort in vivo magic angle magnetic resonance imaging for cell tracking in equine low-field mri
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6942896/
https://www.ncbi.nlm.nih.gov/pubmed/31933650
http://dx.doi.org/10.1155/2019/5670106
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