2D sodium MRI of the human calf using half‐sinc excitation pulses and compressed sensing

Author:

Baker Rebecca R.1ORCID,Muthurangu Vivek1,Rega Marilena2,Montalt‐Tordera Javier1,Rot Samuel34,Solanky Bhavana S.3,Gandini Wheeler‐Kingshott Claudia A. M.356,Walsh Stephen B.7,Steeden Jennifer A.1ORCID

Affiliation:

1. UCL Centre for Translational Cardiovascular Imaging University College London London UK

2. Institute of Nuclear Medicine University College Hospital London UK

3. NMR Research Unit, Queen Square MS Centre, Department of Neuroinflammation, UCL Queen Square Institute of Neurology, Faculty of Brain Sciences University College London London UK

4. Department of Medical Physics and Biomedical Engineering University College London London UK

5. Department of Brain and Behavioral Sciences University of Pavia Pavia Italy

6. Digital Neuroscience Research Unit IRCCS Mondino Foundation Pavia Italy

7. Department of Renal Medicine University College London London UK

Abstract

AbstractPurposeSodium MRI can be used to quantify tissue sodium concentration (TSC) in vivo; however, UTE sequences are required to capture the rapidly decaying signal. 2D MRI enables high in‐plane resolution but typically has long TEs. Half‐sinc excitation may enable UTE; however, twice as many readouts are necessary. Scan time can be minimized by reducing the number of signal averages (NSAs), but at a cost to SNR. We propose using compressed sensing (CS) to accelerate 2D half‐sinc acquisitions while maintaining SNR and TSC.MethodsEx vivo and in vivo TSC were compared between 2D spiral sequences with full‐sinc (TE = 0.73 ms, scan time ≈ 5 min) and half‐sinc excitation (TE = 0.23 ms, scan time ≈ 10 min), with 150 NSAs. Ex vivo, these were compared to a reference 3D sequence (TE = 0.22 ms, scan time ≈ 24 min). To investigate shortening 2D scan times, half‐sinc data was retrospectively reconstructed with fewer NSAs, comparing a nonuniform fast Fourier transform to CS. Resultant TSC and image quality were compared to reference 150 NSAs nonuniform fast Fourier transform images.ResultsTSC was significantly higher from half‐sinc than from full‐sinc acquisitions, ex vivo and in vivo. Ex vivo, half‐sinc data more closely matched the reference 3D sequence, indicating improved accuracy. In silico modeling confirmed this was due to shorter TEs minimizing bias caused by relaxation differences between phantoms and tissue. CS was successfully applied to in vivo, half‐sinc data, maintaining TSC and image quality (estimated SNR, edge sharpness, and qualitative metrics) with ≥50 NSAs.Conclusion2D sodium MRI with half‐sinc excitation and CS was validated, enabling TSC quantification with 2.25 × 2.25 mm2 resolution and scan times of ≤5 mins.

Funder

Ataxia UK

Engineering and Physical Sciences Research Council

Horizon 2020 Framework Programme

Kidney Research UK

Medical Research Council Canada

Rosetrees Trust

University College London Hospitals Biomedical Research Centre

UK Research and Innovation

Wings for Life

Publisher

Wiley

Subject

Radiology, Nuclear Medicine and imaging

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