ECLIPSE utilizing gradient‐modulated offset‐independent adiabaticity (GOIA) pulses for highly selective human brain proton MRSI

• Published in: NMR in biomedicine Vol. 34; no. 1; pp. e4415 - n/a
• Main Authors: Kumaragamage, Chathura, De Feyter, Henk M., Brown, Peter, McIntyre, Scott, Nixon, Terence W., Graaf, Robin A.
• Format: Journal Article
• Language: English
• Published: England Wiley Subscription Services, Inc 01.01.2021
• Subjects: Adiabatic; Adiabatic flow; Algorithms; Bandwidths; Biological products; Brain; Chemical equilibrium; Deposition; ECLIPSE; FID‐MRSI; GOIA; Heterogeneity; human brain; lipid suppression; Lipids; Localization; Metabolites; proton MRSI; Protons; Selectivity; GOIA; human brain; ECLIPSE; lipid suppression; proton MRSI; FID-MRSI
• ISSN: 0952-3480; 1099-1492; 1099-1492
• DOI: 10.1002/nbm.4415

A multitude of extracranial lipid suppression methods exist for proton MRSI acquisitions. Popular and emerging lipid suppression methods each have their inherent set of advantages and disadvantages related to the achievable level of lipid suppression, RF power deposition, insensitivity to B1+ field and lipid T1 heterogeneity, brain coverage, spatial selectivity, chemical shift displacement (CSD) errors and the reliability of spectroscopic data spanning the observed 0.9‐4.7 ppm band. The utility of elliptical localization with pulsed second order fields (ECLIPSE) was previously demonstrated with a greater than 100‐fold in extracranial lipid suppression and low power requirements utilizing 3 kHz bandwidth AFP pulses. Like all gradient‐based localization methods, ECLIPSE is sensitive to CSD errors, resulting in a modified metabolic profile in edge‐of‐ROI voxels. In this work, ECLIPSE is extended with 15 kHz bandwidth second order gradient‐modulated RF pulses based on the gradient offset‐independent adiabaticity (GOIA) algorithm to greatly reduce CSD and improve spatial selectivity. An adiabatic double spin‐echo ECLIPSE inner volume selection (TE = 45 ms) MRSI method and an ECLIPSE outer volume suppression (TE = 3.2 ms) FID‐MRSI method were implemented. Both GOIA‐ECLIPSE MRSI sequences provided artifact‐free metabolite spectra in vivo, with a greater than 100‐fold in lipid suppression and less than 2.6 mm in‐plane CSD and less than 3.3 mm transition width for edge‐of‐ROI voxels, representing an ~5‐fold improvement compared with the parent, nongradient‐modulated method. Despite the 5‐fold larger bandwidth, GOIA‐ECLIPSE only required a 1.9‐fold increase in RF power. The highly robust lipid suppression combined with low CSD and sharp ROI edge transitions make GOIA‐ECLIPSE an attractive alternative to commonly employed lipid suppression methods. Furthermore, the low RF power deposition demonstrates that GOIA‐ECLIPSE is very well suited for high field (≥3 T) MRSI applications. Second order gradient‐modulated RF pulses based on the GOIA algorithm (GOIA‐ECLIPSE) were used to implement two extracranial lipid suppression methods: a TE = 45 ms adiabatic spin echo MRSI and a TE = 3.2 ms FID‐MRSI. Both methods provide a greater than 100‐fold in lipid suppression along with high spatial selectivity, which minimally affects the metabolic profile along ROI edge voxels. The low RF power requirements make GOIA‐ECLIPSE viable for high field (≥3 T) MRSI applications.