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Considerations for ultrasound exposure during transcranial MR acoustic radiation force imaging

The aim of this study was to improve the sensitivity of magnetic resonance-acoustic radiation force imaging (MR-ARFI) to minimize pressures required to localize focused ultrasound (FUS) beams, and to establish safe FUS localization parameters for ongoing ultrasound neuromodulation experiments in liv...

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Autores principales: Phipps, M. Anthony, Jonathan, Sumeeth V., Yang, Pai-Feng, Chaplin, Vandiver, Chen, Li Min, Grissom, William A., Caskey, Charles F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6838326/
https://www.ncbi.nlm.nih.gov/pubmed/31700021
http://dx.doi.org/10.1038/s41598-019-52443-8
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author Phipps, M. Anthony
Jonathan, Sumeeth V.
Yang, Pai-Feng
Chaplin, Vandiver
Chen, Li Min
Grissom, William A.
Caskey, Charles F.
author_facet Phipps, M. Anthony
Jonathan, Sumeeth V.
Yang, Pai-Feng
Chaplin, Vandiver
Chen, Li Min
Grissom, William A.
Caskey, Charles F.
author_sort Phipps, M. Anthony
collection PubMed
description The aim of this study was to improve the sensitivity of magnetic resonance-acoustic radiation force imaging (MR-ARFI) to minimize pressures required to localize focused ultrasound (FUS) beams, and to establish safe FUS localization parameters for ongoing ultrasound neuromodulation experiments in living non-human primates. We developed an optical tracking method to ensure that the MR-ARFI motion-encoding gradients (MEGs) were aligned with a single-element FUS transducer and that the imaged slice was prescribed at the optically tracked location of the acoustic focus. This method was validated in phantoms, which showed that MR-ARFI-derived displacement sensitivity is maximized when the MR-ARFI MEGs were maximally aligned with the FUS propagation direction. The method was then applied in vivo to acquire displacement images in two healthy macaque monkeys (M fascicularis) which showed the FUS beam within the brain. Temperature images were acquired using MR thermometry to provide an estimate of in vivo brain temperature changes during MR-ARFI, and pressure and thermal simulations of the acoustic pulses were performed using the k-Wave package which showed no significant heating at the focus of the FUS beam. The methods presented here will benefit the multitude of transcranial FUS applications as well as future human applications.
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spelling pubmed-68383262019-11-14 Considerations for ultrasound exposure during transcranial MR acoustic radiation force imaging Phipps, M. Anthony Jonathan, Sumeeth V. Yang, Pai-Feng Chaplin, Vandiver Chen, Li Min Grissom, William A. Caskey, Charles F. Sci Rep Article The aim of this study was to improve the sensitivity of magnetic resonance-acoustic radiation force imaging (MR-ARFI) to minimize pressures required to localize focused ultrasound (FUS) beams, and to establish safe FUS localization parameters for ongoing ultrasound neuromodulation experiments in living non-human primates. We developed an optical tracking method to ensure that the MR-ARFI motion-encoding gradients (MEGs) were aligned with a single-element FUS transducer and that the imaged slice was prescribed at the optically tracked location of the acoustic focus. This method was validated in phantoms, which showed that MR-ARFI-derived displacement sensitivity is maximized when the MR-ARFI MEGs were maximally aligned with the FUS propagation direction. The method was then applied in vivo to acquire displacement images in two healthy macaque monkeys (M fascicularis) which showed the FUS beam within the brain. Temperature images were acquired using MR thermometry to provide an estimate of in vivo brain temperature changes during MR-ARFI, and pressure and thermal simulations of the acoustic pulses were performed using the k-Wave package which showed no significant heating at the focus of the FUS beam. The methods presented here will benefit the multitude of transcranial FUS applications as well as future human applications. Nature Publishing Group UK 2019-11-07 /pmc/articles/PMC6838326/ /pubmed/31700021 http://dx.doi.org/10.1038/s41598-019-52443-8 Text en © The Author(s) 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Phipps, M. Anthony
Jonathan, Sumeeth V.
Yang, Pai-Feng
Chaplin, Vandiver
Chen, Li Min
Grissom, William A.
Caskey, Charles F.
Considerations for ultrasound exposure during transcranial MR acoustic radiation force imaging
title Considerations for ultrasound exposure during transcranial MR acoustic radiation force imaging
title_full Considerations for ultrasound exposure during transcranial MR acoustic radiation force imaging
title_fullStr Considerations for ultrasound exposure during transcranial MR acoustic radiation force imaging
title_full_unstemmed Considerations for ultrasound exposure during transcranial MR acoustic radiation force imaging
title_short Considerations for ultrasound exposure during transcranial MR acoustic radiation force imaging
title_sort considerations for ultrasound exposure during transcranial mr acoustic radiation force imaging
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6838326/
https://www.ncbi.nlm.nih.gov/pubmed/31700021
http://dx.doi.org/10.1038/s41598-019-52443-8
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