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Repeatability of Rapid Human Cardiac Phosphorus MRSI ( 31 P ‐ MRSI ) Using Concentric Ring Trajectory Readouts at 7 T

Abstract:
Purpose: PCr/ATP ratio is determined at 7 T typically using Fourier‐transform based magnetic resonance spectroscopic imaging sequences (FT‐MRSI). These sequences require acquisition times longer than desirable for inclusion in cardiac clinical trials. Concentric ring trajectory (CRT‐MRSI) has been described as an accelerated alternative k‐space sampling method. In this work we aim to establish the inter‐ and intra‐session repeatability of three different CRT protocols and compare their voxel‐based PCr/ATP ratios to compartment‐based PCr/ATP values extracted with spectroscopy using a linear algebraic model (SLAM) method. Methods: Seven healthy volunteers were scanned twice on two different days. Each time a 6.5‐min 3D FT‐MRSI acquisition with 10 × 10 × 10 resolution was followed by a 2.5‐min CRT‐MRSI with matched resolution, a 1.5‐min CRT‐MRSI with matched resolution, and a 6.9‐min CRT‐MRSI with 12 × 12 × 12 resolution. Spectra from a mid‐septal voxel and the cardiac compartment were fitted with the OXSA toolbox. PCr/ATP ratio was quantified for inter‐ and intra‐session repeatability analysis. Results: Paired repeated measurements were not significantly different within subjects. Good inter‐ and intra‐session agreement was observed between FT‐MRSI and each CRT‐MRSI protocol. CRT‐MRSI protocols all had larger coefficients of repeatability (CoR) than FT‐MRSI. CRT‐SLAM‐based PCr/ATP values had lower CoR than voxel‐based data except for 2.5‐min CRT‐SLAM, and high‐resolution CRT‐SLAM had lower inter‐session CoR compared to FT‐MRSI (1.42 vs. 2.21). Conclusion: We established the repeatability of CRT‐MRSI‐based PCr/ATP values and showed higher SNR and lower CoR for CRT‐SLAM. Our findings allow shorter 31P MRS acquisition times and the use of more advanced energetics‐probing techniques in clinical studies.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1002/mrm.70220

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Institution:
University of Oxford
Division:
MSD
Department:
Radcliffe Department of Medicine
Sub department:
RDM-Strategic
Role:
Author
ORCID:
0000-0002-1361-4349
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Institution:
University of Oxford
Role:
Author
ORCID:
0000-0001-7159-7025
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Role:
Author
ORCID:
0000-0002-3857-0119
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Role:
Author
ORCID:
0000-0003-1235-7595


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Funder identifier:
https://ror.org/04txyc737
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Funder identifier:
https://ror.org/037nx0e70
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Funder identifier:
https://ror.org/05m8dr349
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Funder identifier:
https://ror.org/029chgv08


Publisher:
Wiley
Journal:
Magnetic Resonance in Medicine More from this journal
Publication date:
2025-12-08
Acceptance date:
2025-11-28
DOI:
EISSN:
1522-2594
ISSN:
0740-3194


Language:
English
Keywords:
Pubs id:
2350430
UUID:
uuid_3602baa7-03c2-456d-b745-cab53c13b84b
Local pid:
pubs:2350430
Source identifiers:
3547579
Deposit date:
2025-12-09
ARK identifier:
This ORA record was generated from metadata provided by an external service. It has not been edited by the ORA Team.

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