Abstract

Phosphorus (31P) MRSI provides opportunities to monitor potential biomarkers. However, current applications of 31P MRS are generally restricted to relatively small volumes as small coils are used. Conventional surface coils require high energy adiabatic RF pulses to achieve flip angle homogeneity, leading to high specific absorption rates (SARs), and occupy space within the MRI bore. A birdcage coil behind the bore cover can potentially reduce the SAR constraints massively by use of conventional amplitude modulated pulses without sacrificing patient space. Here, we demonstrate that the integrated 31P birdcage coil setup with a high power RF amplifier at 7 T allows for low flip angle excitations with short repetition time (T R) for fast 3D chemical shift imaging (CSI) and 3D T 1‐weighted CSI as well as high flip angle multi‐refocusing pulses, enabling multi‐echo CSI that can measure metabolite T 2, over a large field of view in the body. B 1 + calibration showed a variation of only 30% in maximum B 1 in four volunteers. High signal‐to‐noise ratio (SNR) MRSI was obtained in the gluteal muscle using two fast in vivo 3D spectroscopic imaging protocols, with low and high flip angles, and with multi‐echo MRSI without exceeding SAR levels. In addition, full liver MRSI was achieved within SAR constraints. The integrated 31P body coil allowed for fast spectroscopic imaging and successful implementation of the multi‐echo method in the body at 7 T. Moreover, no additional enclosing hardware was needed for 31P excitation, paving the way to include larger subjects and more space for receiver arrays. The increase in possible number of RF excitations per scan time, due to the improved B 1 + homogeneity and low SAR, allows SNR to be exchanged for spatial resolution in CSI and/or T 1 weighting by simply manipulating T R and/or flip angle to detect and quantify ratios from different molecular species.

Highlights

  • Phosphorus (31P) MRSI provides opportunities to monitor tissue metabolism by measuring specific energy metabolites and phospholipid metabolites

  • All subjects fitted well in the 31P whole‐body coil setup, as this coil is integrated within the MRI scanner, behind the covers of the bore, providing sufficient space for the dipole transceivers and receive loops as shown in Figure 1A and 1B

  • The flip angle sweep acquired in four volunteers for B1+ calibration of the 31P whole‐body coil is shown in Figure 2; the average variation in maximum B1 between the volunteers was 30% using 23 kW as peak power

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Summary

Introduction

Phosphorus (31P) MRSI provides opportunities to monitor tissue metabolism by measuring specific energy metabolites and phospholipid metabolites. Phosphomonoesters (PMEs) and phosphodiesters (PDEs) allow assessment of phospholipid metabolism.[4,5,6] At ultra‐high field (>7 T), the increased signal‐to‐noise ratio (SNR) and increased spectral resolution facilitate the individual detection of PMEs (phosphocholine (PC), phosphoethanolamine (PE)) and PDEs (glycerophosphocholine (GPC), glycerophosphoethanolamine (GPE)).[7] Enhanced PME to PDE ratios (PC to GPC, PE to GPE) are indicative of proliferation and are often seen in tumor tissue[5,6,8,9,10,11,12,13] Changes in these ratios during (chemo)therapy are markers of therapy response and take place well before morphological changes can be observed.[14,15,16]

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