Dataset Information

Suppression of skeletal muscle signal using a crusher coil: A human cardiac (31) p-MR spectroscopy study at 7 tesla.

ABSTRACT:

Purpose

The translation of sophisticated phosphorus MR spectroscopy ((31)P-MRS) protocols to 7 Tesla (T) is particularly challenged by the issue of radiofrequency (RF) heating. Legal limits on RF heating make it hard to reliably suppress signals from skeletal muscle that can contaminate human cardiac (31)P spectra at 7T. We introduce the first surface-spoiling crusher coil for human cardiac (31)P-MRS at 7T.

Methods

A planar crusher coil design was optimized with simulations and its performance was validated in phantoms. Crusher gradient pulses (100 ?s) were then applied during human cardiac (31)P-MRS at 7T.

Results

In a phantom, residual signals were 50 ± 10% with BISTRO (B1 -insensitive train to obliterate signal), and 34 ± 8% with the crusher coil. In vivo, residual signals in skeletal muscle were 49 ± 4% using BISTRO, and 24 ± 5% using the crusher coil. Meanwhile, in the interventricular septum, spectral quality and metabolite quantification did not differ significantly between BISTRO (phosphocreatine/adenosine triphosphate [PCr/ATP]?= 2.1 ± 0.4) and the crusher coil (PCr/ATP = 1.8 ± 0.4). However, the specific absorption rate (SAR) decreased from 96 ± 1% of the limit (BISTRO) to 16 ± 1% (crusher coil).

Conclusion

A crusher coil is an SAR-efficient alternative for selectively suppressing skeletal muscle during cardiac (31)P-MRS at 7T. A crusher coil allows the use of sequence modules that would have been SAR-prohibitive, without compromising skeletal muscle suppression.

SUBMITTER: Schaller B

PROVIDER: S-EPMC4762536 | biostudies-literature | 2016 Mar

REPOSITORIES: biostudies-literature

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Publications

Suppression of skeletal muscle signal using a crusher coil: A human cardiac (31) p-MR spectroscopy study at 7 tesla.

Schaller Benoit B Clarke William T WT Neubauer Stefan S Robson Matthew D MD Rodgers Christopher T CT

Magnetic resonance in medicine 20150428 3

<h4>Purpose</h4>The translation of sophisticated phosphorus MR spectroscopy ((31)P-MRS) protocols to 7 Tesla (T) is particularly challenged by the issue of radiofrequency (RF) heating. Legal limits on RF heating make it hard to reliably suppress signals from skeletal muscle that can contaminate human cardiac (31)P spectra at 7T. We introduce the first surface-spoiling crusher coil for human cardiac (31)P-MRS at 7T.<h4>Methods</h4>A planar crusher coil design was optimized with simulations and it ...[more]

PMID: 25924813

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Project description:PurposePhosphorus (31 P) metabolites are emerging liver disease biomarkers. Of particular interest are phosphomonoester and phosphodiester (PDE) "peaks" that comprise multiple overlapping resonances in 31 P spectra. This study investigates the effect of improved spectral resolution at 7 Tesla (T) on quantifying hepatic metabolites in cirrhosis.MethodsFive volunteers were scanned to determine metabolite T1 s. Ten volunteers and 11 patients with liver cirrhosis were scanned at 7T. Liver spectra were acquired in 28 min using a 16-channel 31 P array and 3D chemical shift imaging. Concentrations were calculated using γ-adenosine-triphosphate (γ-ATP) = 2.65 mmol/L wet tissue.ResultsT1 means ± standard deviations: phosphatidylcholine 1.05 ± 0.28 s, nicotinamide-adenine-dinucleotide (NAD+ ) 2.0 ± 1.0 s, uridine-diphosphoglucose (UDPG) 3.3 ± 1.4 s. Concentrations in healthy volunteers: α-ATP 2.74 ± 0.11 mmol/L wet tissue, inorganic phosphate 2.23 ± 0.20 mmol/L wet tissue, glycerophosphocholine 2.34 ± 0.46 mmol/L wet tissue, glycerophosphoethanolamine 1.50 ± 0.28 mmol/L wet tissue, phosphocholine 1.06 ± 0.16 mmol/L wet tissue, phosphoethanolamine 0.77 ± 0.14 mmol/L wet tissue, NAD+ 2.37 ± 0.14 mmol/L wet tissue, UDPG 2.00 ± 0.22 mmol/L wet tissue, phosphatidylcholine 1.38 ± 0.31 mmol/L wet tissue. Inorganic phosphate and phosphatidylcholine concentrations were significantly lower in patients; glycerophosphoethanolamine concentrations were significantly higher (P < 0.05).ConclusionWe report human in vivo hepatic T1 s for phosphatidylcholine, NAD+ , and UDPG for the first time at 7T. Our protocol allows high signal-to-noise, repeatable measurement of metabolite concentrations in human liver. The splitting of PDE into its constituent peaks at 7T may allow more insight into changes in metabolism. Magn Reson Med 78:2095-2105, 2017. © 2017 The Authors Magnetic Resonance in Medicine published by Wiley Periodicals, Inc. on behalf of International Society for Magnetic Resonance in Medicine. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

Project description:Parallel imaging using phased array coils facilitates accelerated magnetic resonance imaging (MRI) and spectroscopy (MRS). Parallel data reconstruction requires the combination of data from individual coil elements, but limited combination algorithms currently exist for higher-order phased arrays and MRS data. Here, we present a systematic framework for identifying coil proximity-related signal inhomogeneities and noise levels in phased array coils that may affect sensitivity of parallel MRS. Single-voxel MRS was acquired in nine voxel positions in a brain spectroscopy phantom on a 3T whole-body MR scanner using commercially available 64-, 32-, and 20-channel phased array coils. Spectra produced by individual coil elements were combined using both a signal-to-noise ratio (SNR) threshold and based on the position of individual coil elements. SNR and metabolite Cramer-Rao lower bounds (CRLBs) from the final combined spectra were used as metrics to compare combination strategies and the effects of the phased array geometry and individual coil proximity. Comparisons were performed using one-way repeated measures ANOVA and post-hoc Tukey's range test (p<0.05). The 32-channel phased array coil produced the highest overall SNR compared to the 64-channel (p=0.0009) or 20-channel coils (p=0.003). Low SNR spectra from individual coil elements in the 64-channel coil can reduce the overall SNR when simply combining spectra from all elements. SNR varied significantly as a function of voxel position (F=58.3, p<0.0001) and SNR threshold for all phased arrays (p<0.05 for 64-, 32-, and 20-channel coils). Metabolite CRLBs were dependent on the combination strategy. We demonstrate the importance of the sampling voxel position and coil proximity on overall SNR in parallel MRS data acquisition, with significant SNR improvements after selectively filtering individual spectra based on pre-determined SNR thresholds which must be optimized for each phased array coil element and volume of interest.

Dataset Information

Suppression of skeletal muscle signal using a crusher coil: A human cardiac (31) p-MR spectroscopy study at 7 tesla.

Purpose

Methods

Results

Conclusion

Publications

Suppression of skeletal muscle signal using a crusher coil: A human cardiac (31) p-MR spectroscopy study at 7 tesla.

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