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Reproducibility of human cardiac phosphorus MRS ((31)P‐MRS) at 7 T
PURPOSE: We test the reproducibility of human cardiac phosphorus MRS ((31)P‐MRS) at ultra‐high field strength (7 T) for the first time. The primary motivation of this work was to assess the reproducibility of a ‘rapid’ 6½ min (31)P three‐dimensional chemical shift imaging (3D‐CSI) sequence, which if...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6546607/ https://www.ncbi.nlm.nih.gov/pubmed/30924566 http://dx.doi.org/10.1002/nbm.4095 |
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author | Ellis, Jane Valkovič, Ladislav Purvis, Lucian A.B. Clarke, William T. Rodgers, Christopher T. |
author_facet | Ellis, Jane Valkovič, Ladislav Purvis, Lucian A.B. Clarke, William T. Rodgers, Christopher T. |
author_sort | Ellis, Jane |
collection | PubMed |
description | PURPOSE: We test the reproducibility of human cardiac phosphorus MRS ((31)P‐MRS) at ultra‐high field strength (7 T) for the first time. The primary motivation of this work was to assess the reproducibility of a ‘rapid’ 6½ min (31)P three‐dimensional chemical shift imaging (3D‐CSI) sequence, which if sufficiently reproducible would allow the study of stress‐response processes. We compare this with an established 28 min protocol, designed to record high‐quality spectra in a clinically feasible scan time. Finally, we use this opportunity to compare the effect of per‐subject B (0) shimming on data quality and reproducibility in the 6½ min protocol. METHODS: 10 healthy subjects were scanned on two occasions: one to test the 28 min 3D‐CSI protocol, and one to test the 6½ min protocol. Spectra were fitted using the OXSA MATLAB toolbox. The phosphocreatine to adenosine triphosphate concentration ratio (PCr/ATP) from each scan was analysed for intra‐ and intersubject variability. The impact of different strategies for voxel selection was assessed. RESULTS: There were no significant differences between repeated measurements in the same subject. For the 28 min protocol, PCr/ATP in the midseptal voxel across all scans was 1.91 ± 0.36 (mean ± intersubject SD). For the 6½ min protocol, PCr/ATP in the midseptal voxel was 1.76 ± 0.40. The coefficients of reproducibility (CRs) were 0.49 (28 min) and 0.67 (6½ min). Per‐subject B (0) shimming improved the fitted PCr/ATP precision (for 6½ min scans), but had negligible effect on the CR (0.67 versus 0.66). CONCLUSIONS: Both 7 T protocols show improved reproducibility compared with a previous 3 T study by Tyler et al. Our results will enable informed power calculations and protocol selection for future clinical research studies. |
format | Online Article Text |
id | pubmed-6546607 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-65466072019-06-03 Reproducibility of human cardiac phosphorus MRS ((31)P‐MRS) at 7 T Ellis, Jane Valkovič, Ladislav Purvis, Lucian A.B. Clarke, William T. Rodgers, Christopher T. NMR Biomed Research Articles PURPOSE: We test the reproducibility of human cardiac phosphorus MRS ((31)P‐MRS) at ultra‐high field strength (7 T) for the first time. The primary motivation of this work was to assess the reproducibility of a ‘rapid’ 6½ min (31)P three‐dimensional chemical shift imaging (3D‐CSI) sequence, which if sufficiently reproducible would allow the study of stress‐response processes. We compare this with an established 28 min protocol, designed to record high‐quality spectra in a clinically feasible scan time. Finally, we use this opportunity to compare the effect of per‐subject B (0) shimming on data quality and reproducibility in the 6½ min protocol. METHODS: 10 healthy subjects were scanned on two occasions: one to test the 28 min 3D‐CSI protocol, and one to test the 6½ min protocol. Spectra were fitted using the OXSA MATLAB toolbox. The phosphocreatine to adenosine triphosphate concentration ratio (PCr/ATP) from each scan was analysed for intra‐ and intersubject variability. The impact of different strategies for voxel selection was assessed. RESULTS: There were no significant differences between repeated measurements in the same subject. For the 28 min protocol, PCr/ATP in the midseptal voxel across all scans was 1.91 ± 0.36 (mean ± intersubject SD). For the 6½ min protocol, PCr/ATP in the midseptal voxel was 1.76 ± 0.40. The coefficients of reproducibility (CRs) were 0.49 (28 min) and 0.67 (6½ min). Per‐subject B (0) shimming improved the fitted PCr/ATP precision (for 6½ min scans), but had negligible effect on the CR (0.67 versus 0.66). CONCLUSIONS: Both 7 T protocols show improved reproducibility compared with a previous 3 T study by Tyler et al. Our results will enable informed power calculations and protocol selection for future clinical research studies. John Wiley and Sons Inc. 2019-03-29 2019-06 /pmc/articles/PMC6546607/ /pubmed/30924566 http://dx.doi.org/10.1002/nbm.4095 Text en © 2019 The Authors. NMR in Biomedicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Ellis, Jane Valkovič, Ladislav Purvis, Lucian A.B. Clarke, William T. Rodgers, Christopher T. Reproducibility of human cardiac phosphorus MRS ((31)P‐MRS) at 7 T |
title | Reproducibility of human cardiac phosphorus MRS ((31)P‐MRS) at 7 T |
title_full | Reproducibility of human cardiac phosphorus MRS ((31)P‐MRS) at 7 T |
title_fullStr | Reproducibility of human cardiac phosphorus MRS ((31)P‐MRS) at 7 T |
title_full_unstemmed | Reproducibility of human cardiac phosphorus MRS ((31)P‐MRS) at 7 T |
title_short | Reproducibility of human cardiac phosphorus MRS ((31)P‐MRS) at 7 T |
title_sort | reproducibility of human cardiac phosphorus mrs ((31)p‐mrs) at 7 t |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6546607/ https://www.ncbi.nlm.nih.gov/pubmed/30924566 http://dx.doi.org/10.1002/nbm.4095 |
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