Abstract

In localized MRS, spurious echo artifacts commonly occur when unsuppressed signal outside the volume of interest is excited and refocused. In the spectral domain, these signals often overlap with metabolite resonances and hinder accurate quantification. Because the artifacts originate from regions separate from the target MRS voxel, this work proposes that sensitivity encoding based on receive-coil sensitivity profiles may be used to separate these signal contributions. Numerical simulations were performed to explore the effect of sensitivity-encoded separation for unknown artifact regions. An imaging-based approach was developed to identify regions that may contribute to spurious echo artifacts, and tested for sensitivity-based unfolding of signal on six data sets from three brain regions. Spectral data reconstructed using the proposed method ("ERASE") were compared with the standard coil combination. The method was able to fully unfold artifact signals if regions were known a priori. Mismatch between estimated and true artifact regions reduced the efficiency of removal, yet metabolite signals were unaffected. Water suppression imaging was able to identify regions of unsuppressed signal, and ERASE (from up to eight regions) led to visible removal of artifacts relative to standard reconstruction. Fitting errors across major metabolites were also lower; for example, Cramér-Rao lower bounds of myo-inositol were 13.7% versus 17.5% for ERASE versus standard reconstruction, respectively. The ERASE reconstruction tool was demonstrated to reduce spurious echo artifacts in single-voxel MRS. This tool may be incorporated into standard workflows to improve spectral quality when hardware limitations or other factors result in out-of-voxel signal contamination.

Highlights

  • Robust quantification of metabolite concentrations in single-­ voxel MRS of the brain is critically dependent on spectral quality

  • Fitting errors were significantly lower using ERASE compared with the standard combination for all major metabolites, apart from glutamate plus glutamine (11.7% vs 14.7%; P = .06), which was very close to significance: total N-­acetyl aspartate (5.6% vs 7.0%; P = .03), total choline (10.7% vs 14.1%; P = .019), total creatine (7.0% vs 9.2%; P = .04), and mI (13.7% vs 17.5%; P = .03)

  • Across six in vivo data sets acquired in three different brain regions, the proposed ERASE method visibly improved spectral quality compared with standard reconstruction of multichannel MRS data, in particular over the 3-­4 ppm region

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Summary

Introduction

Robust quantification of metabolite concentrations in single-­ voxel MRS of the brain is critically dependent on spectral quality. One commonly observed artifact is the spurious echo. The spurious echo manifests as an oscillatory or “beating” signal that spans a range of frequencies and often overlaps with metabolite resonances, and is referred to as “ghosting artifact.”. Given the sizeable concentration difference between water and metabolites in 1H-M­ RS of brain (~104), the main contribution to the spurious echo artifact arises from regions of unsuppressed water signal,[3] lipid resonances may form spurious echoes

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