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 inNMR in biomedicine Vol. 34; no. 5; pp. e4236 - n/a
Main Authors Öz, Gülin, Deelchand, Dinesh K., Wijnen, Jannie P., Mlynárik, Vladimír, Xin, Lijing, Mekle, Ralf, Noeske, Ralph, Scheenen, Tom W.J., Tkáč, Ivan, Andronesi, Ovidiu, Barker, Peter B., Bartha, Robert, Berrington, Adam, Boer, Vincent, Cudalbu, Christina, Emir, Uzay E., Ernst, Thomas, Fillmer, Ariane, Heerschap, Arend, Henry, Pierre‐Gilles, Hurd, Ralph E., Joers, James M., Juchem, Christoph, Kan, Hermien E., Klomp, Dennis W. J., Kreis, Roland, Landheer, Karl, Mangia, Silvia, Marjańska, Małgorzata, Near, Jamie, Ratai, Eva M., Ronen, Itamar, Slotboom, Johannes, Soher, Brian J., Terpstra, Melissa, Valette, Julien, Van der Graaf, Marinette, Wilson, Martin
Format Journal Article
LanguageEnglish
Published Oxford Wiley Subscription Services, Inc 01.05.2021
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Online AccessGet full text
ISSN0952-3480
1099-1492
DOI10.1002/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.
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
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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...
SourceID pubmedcentral
proquest
wiley
SourceType Open Access Repository
Aggregation Database
Publisher
StartPage e4236
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
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fnbm.4236
https://www.proquest.com/docview/2514208936
https://pubmed.ncbi.nlm.nih.gov/PMC7347431
Volume 34
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