Advanced single voxel 1H magnetic resonance spectroscopy techniques in humans: Experts' consensus recommendations
Conventional proton MRS has been successfully utilized to noninvasively assess tissue biochemistry in conditions that result in large changes in metabolite levels. For more challenging applications, namely, in conditions which result in subtle metabolite changes, the limitations of vendor‐provided M...
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Published in | NMR in biomedicine Vol. 34; no. 5; pp. e4236 - n/a |
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Main Authors | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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Oxford
Wiley Subscription Services, Inc
01.05.2021
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Online Access | Get full text |
ISSN | 0952-3480 1099-1492 |
DOI | 10.1002/nbm.4236 |
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Abstract | Conventional proton MRS has been successfully utilized to noninvasively assess tissue biochemistry in conditions that result in large changes in metabolite levels. For more challenging applications, namely, in conditions which result in subtle metabolite changes, the limitations of vendor‐provided MRS protocols are increasingly recognized, especially when used at high fields (≥3 T) where chemical shift displacement errors, B0 and B1 inhomogeneities and limitations in the transmit B1 field become prominent. To overcome the limitations of conventional MRS protocols at 3 and 7 T, the use of advanced MRS methodology, including pulse sequences and adjustment procedures, is recommended. Specifically, the semiadiabatic LASER sequence is recommended when TE values of 25‐30 ms are acceptable, and the semiadiabatic SPECIAL sequence is suggested as an alternative when shorter TE values are critical. The magnetic field B0 homogeneity should be optimized and RF pulses should be calibrated for each voxel. Unsuppressed water signal should be acquired for eddy current correction and preferably also for metabolite quantification. Metabolite and water data should be saved in single shots to facilitate phase and frequency alignment and to exclude motion‐corrupted shots. Final averaged spectra should be evaluated for SNR, linewidth, water suppression efficiency and the presence of unwanted coherences. Spectra that do not fit predefined quality criteria should be excluded from further analysis. Commercially available tools to acquire all data in consistent anatomical locations are recommended for voxel prescriptions, in particular in longitudinal studies. To enable the larger MRS community to take advantage of these advanced methods, a list of resources for these advanced protocols on the major clinical platforms is provided. Finally, a set of recommendations are provided for vendors to enable development of advanced MRS on standard platforms, including implementation of advanced localization sequences, tools for quality assurance on the scanner, and tools for prospective volume tracking and dynamic linear shim corrections.
Vendor‐provided MRS protocols suffer from multiple limitations at high and ultrahigh fields (≥3 T), including increased chemical shift displacement errors, increased B0 and B1 inhomogeneities and insufficient transmit B1 field. We provide an overview of two advanced MRS sequences, sLASER and SPECIAL, which largely overcome the limitations of conventional MRS protocols. We provide guidelines for their use, quality assurance and quality control, and a set of recommendations for vendors to enable advanced MRS on standard platforms. |
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AbstractList | Conventional proton MRS has been successfully utilized to non-invasively assess tissue biochemistry in conditions that result in large changes in metabolite levels. For more challenging applications, namely in conditions that result in subtle metabolite changes, the limitations of vendor-provided MRS protocols are increasingly recognized, especially when used at high fields (≥ 3 tesla) where chemical shift displacement errors, B
0
and B
1
inhomogeneities and limitations in transmit B
1
field become prominent. To overcome the limitations of conventional MRS protocols at 3T and 7T, use of advanced MRS methodology, including pulse sequences and adjustment procedures, is recommended. Specifically, the semi-LASER sequence is recommended when T
E
values of 25–30ms are acceptable, and the semi-adiabatic SPECIAL sequence is suggested as an alternative when shorter T
E
values are critical. The magnetic field B
0
homogeneity should be optimized and RF pulses should be calibrated for each voxel. Unsuppressed water signal should be acquired for eddy current correction and preferably also for metabolite quantification. Metabolite and water data should be saved in single shots to facilitate phase and frequency alignment and to exclude motion-corrupted shots. Final averaged spectra should be evaluated for SNR, linewidth, water suppression efficiency and presence of unwanted coherences. Spectra that do not fit predefined quality criteria should be excluded from further analysis. Commercially available tools to acquire all data in consistent anatomical locations are recommended for voxel prescriptions, in particular in longitudinal studies. To enable the larger MRS community to take advantage of these advanced methods, a list of resources for these advanced protocols on the major clinical platforms is provided. Finally, a set of recommendations are provided for vendors to enable development of advanced MRS on standard platforms, including implementation of advanced localization sequences, tools for quality assurance on the scanner, and tools for prospective volume tracking and dynamic linear shim corrections.
Vendor-provided MRS protocols suffer from multiple limitations at high and ultra-high field (≥ 3T), including increased chemical shift displacement errors, increased B
0
and B
1
inhomogeneities and insufficient transmit B
1
field. We provide an overview of two advanced MRS sequences, semi-LASER and SPECIAL, that largely overcome the limitations of conventional MRS protocols. We provide guidelines for their use, quality assurance and quality control, and finally a set of recommendations for vendors to enable advanced MRS on standard platforms. Conventional proton MRS has been successfully utilized to noninvasively assess tissue biochemistry in conditions that result in large changes in metabolite levels. For more challenging applications, namely, in conditions which result in subtle metabolite changes, the limitations of vendor‐provided MRS protocols are increasingly recognized, especially when used at high fields (≥3 T) where chemical shift displacement errors, B0 and B1 inhomogeneities and limitations in the transmit B1 field become prominent. To overcome the limitations of conventional MRS protocols at 3 and 7 T, the use of advanced MRS methodology, including pulse sequences and adjustment procedures, is recommended. Specifically, the semiadiabatic LASER sequence is recommended when TE values of 25‐30 ms are acceptable, and the semiadiabatic SPECIAL sequence is suggested as an alternative when shorter TE values are critical. The magnetic field B0 homogeneity should be optimized and RF pulses should be calibrated for each voxel. Unsuppressed water signal should be acquired for eddy current correction and preferably also for metabolite quantification. Metabolite and water data should be saved in single shots to facilitate phase and frequency alignment and to exclude motion‐corrupted shots. Final averaged spectra should be evaluated for SNR, linewidth, water suppression efficiency and the presence of unwanted coherences. Spectra that do not fit predefined quality criteria should be excluded from further analysis. Commercially available tools to acquire all data in consistent anatomical locations are recommended for voxel prescriptions, in particular in longitudinal studies. To enable the larger MRS community to take advantage of these advanced methods, a list of resources for these advanced protocols on the major clinical platforms is provided. Finally, a set of recommendations are provided for vendors to enable development of advanced MRS on standard platforms, including implementation of advanced localization sequences, tools for quality assurance on the scanner, and tools for prospective volume tracking and dynamic linear shim corrections. Vendor‐provided MRS protocols suffer from multiple limitations at high and ultrahigh fields (≥3 T), including increased chemical shift displacement errors, increased B0 and B1 inhomogeneities and insufficient transmit B1 field. We provide an overview of two advanced MRS sequences, sLASER and SPECIAL, which largely overcome the limitations of conventional MRS protocols. We provide guidelines for their use, quality assurance and quality control, and a set of recommendations for vendors to enable advanced MRS on standard platforms. Conventional proton MRS has been successfully utilized to noninvasively assess tissue biochemistry in conditions that result in large changes in metabolite levels. For more challenging applications, namely, in conditions which result in subtle metabolite changes, the limitations of vendor‐provided MRS protocols are increasingly recognized, especially when used at high fields (≥3 T) where chemical shift displacement errors, B0 and B1 inhomogeneities and limitations in the transmit B1 field become prominent. To overcome the limitations of conventional MRS protocols at 3 and 7 T, the use of advanced MRS methodology, including pulse sequences and adjustment procedures, is recommended. Specifically, the semiadiabatic LASER sequence is recommended when TE values of 25‐30 ms are acceptable, and the semiadiabatic SPECIAL sequence is suggested as an alternative when shorter TE values are critical. The magnetic field B0 homogeneity should be optimized and RF pulses should be calibrated for each voxel. Unsuppressed water signal should be acquired for eddy current correction and preferably also for metabolite quantification. Metabolite and water data should be saved in single shots to facilitate phase and frequency alignment and to exclude motion‐corrupted shots. Final averaged spectra should be evaluated for SNR, linewidth, water suppression efficiency and the presence of unwanted coherences. Spectra that do not fit predefined quality criteria should be excluded from further analysis. Commercially available tools to acquire all data in consistent anatomical locations are recommended for voxel prescriptions, in particular in longitudinal studies. To enable the larger MRS community to take advantage of these advanced methods, a list of resources for these advanced protocols on the major clinical platforms is provided. Finally, a set of recommendations are provided for vendors to enable development of advanced MRS on standard platforms, including implementation of advanced localization sequences, tools for quality assurance on the scanner, and tools for prospective volume tracking and dynamic linear shim corrections. |
Author | Noeske, Ralph Hurd, Ralph E. Soher, Brian J. Mangia, Silvia Öz, Gülin Emir, Uzay E. Ernst, Thomas Fillmer, Ariane Terpstra, Melissa Xin, Lijing Landheer, Karl Valette, Julien Slotboom, Johannes Wilson, Martin Deelchand, Dinesh K. Tkáč, Ivan Wijnen, Jannie P. Barker, Peter B. Henry, Pierre‐Gilles Juchem, Christoph Marjańska, Małgorzata Mekle, Ralf Near, Jamie Ratai, Eva M. Klomp, Dennis W. J. Kreis, Roland Cudalbu, Christina Boer, Vincent Andronesi, Ovidiu Heerschap, Arend Ronen, Itamar Bartha, Robert Mlynárik, Vladimír Berrington, Adam Joers, James M. Scheenen, Tom W.J. Kan, Hermien E. Van der Graaf, Marinette |
AuthorAffiliation | 6 GE Healthcare, Berlin, Germany 7 Department of Radiology and Nuclear Medicine, Radboud University Medical Center, Nijmegen, the Netherlands 4 Animal Imaging and Technology Core (AIT), Center for Biomedical Imaging (CIBM), École Polytechnique Fédérale de Lausanne, Lausanne, Switzerland 5 Center for Stroke Research Berlin (CSB), Charité Universitätsmedizin Berlin, Berlin, Germany 8 Erwin L Hahn Institute for Magnetic Resonance Imaging, UNESCO World Cultural Heritage Zollverein, Essen, Germany 1 Center for Magnetic Resonance Research, Department of Radiology, University of Minnesota, Minneapolis, MN 55455, United States 2 High field MR Research group, Department of Radiology, University Medical Centre Utrecht, Utrecht, the Netherlands 3 High Field MR Centre, Department of Biomedical Imaging and Image-Guided Therapy, Medical University of Vienna, Vienna, Austria |
AuthorAffiliation_xml | – name: 6 GE Healthcare, Berlin, Germany – name: 4 Animal Imaging and Technology Core (AIT), Center for Biomedical Imaging (CIBM), École Polytechnique Fédérale de Lausanne, Lausanne, Switzerland – name: 2 High field MR Research group, Department of Radiology, University Medical Centre Utrecht, Utrecht, the Netherlands – name: 8 Erwin L Hahn Institute for Magnetic Resonance Imaging, UNESCO World Cultural Heritage Zollverein, Essen, Germany – name: 5 Center for Stroke Research Berlin (CSB), Charité Universitätsmedizin Berlin, Berlin, Germany – name: 3 High Field MR Centre, Department of Biomedical Imaging and Image-Guided Therapy, Medical University of Vienna, Vienna, Austria – name: 7 Department of Radiology and Nuclear Medicine, Radboud University Medical Center, Nijmegen, the Netherlands – name: 1 Center for Magnetic Resonance Research, Department of Radiology, University of Minnesota, Minneapolis, MN 55455, United States |
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Snippet | Conventional proton MRS has been successfully utilized to noninvasively assess tissue biochemistry in conditions that result in large changes in metabolite... Conventional proton MRS has been successfully utilized to non-invasively assess tissue biochemistry in conditions that result in large changes in metabolite... |
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SubjectTerms | Biological products body brain Chemical equilibrium chemical shift displacement Eddy currents Homogeneity Localization Longitudinal studies Magnetic fields Magnetic resonance spectroscopy Metabolites Platforms Quality assurance Reproducibility semiadiabatic LASER shimming SPECIAL Spectrum analysis |
Title | Advanced single voxel 1H magnetic resonance spectroscopy techniques in humans: Experts' consensus recommendations |
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