Concentration and effective T2 relaxation times of macromolecules at 3T
Purpose We aimed to investigate the concentration and effective T2 relaxation time of macromolecules assessed with an ultra‐short TE sLASER sequence in 2 brain regions, the occipital and frontal cortex, in both genders at 3T. Methods An optimized sLASER sequence was used in conjunction with a double...
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Published in | Magnetic resonance in medicine Vol. 84; no. 5; pp. 2327 - 2337 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Hoboken
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01.11.2020
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ISSN | 0740-3194 1522-2594 1522-2594 |
DOI | 10.1002/mrm.28282 |
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Abstract | Purpose
We aimed to investigate the concentration and effective T2 relaxation time of macromolecules assessed with an ultra‐short TE sLASER sequence in 2 brain regions, the occipital and frontal cortex, in both genders at 3T.
Methods
An optimized sLASER sequence was used in conjunction with a double‐inversion preparation module to null the metabolites. Eight equally spaced TEs were chosen from 20.1 to 62.1 ms, and the macromolecules were modeled by 10 line broadened singlets. The amplitude of each of the macromolecule signals was extracted at each TE and fit to a monoexponential function to extract the respective effective T2 values. Absolute quantification of the macromolecule resonances was performed using water signal as a reference. A total of 10 young healthy adult subjects (5 females) were scanned, with spectra being obtained from both the frontal and occipital cortex. Differences in the effective T2 relaxation times and concentrations were investigated between both regions and genders.
Results
A wide disparity was observed between the effective T2 values of the individual resonances; however, no significant differences between gender or region for any of the measured macromolecule concentration or effective T2 values were found.
Conclusion
The effective T2 relaxation times and concentration of 10 different macromolecule resonances were measured and found to be well represented by the monoexponential model. These results will be useful for absolute quantification of macromolecules in future studies, or in the generation of synthetic basis sets for optimization or machine learning. |
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AbstractList | PurposeWe aimed to investigate the concentration and effective T2 relaxation time of macromolecules assessed with an ultra‐short TE sLASER sequence in 2 brain regions, the occipital and frontal cortex, in both genders at 3T.MethodsAn optimized sLASER sequence was used in conjunction with a double‐inversion preparation module to null the metabolites. Eight equally spaced TEs were chosen from 20.1 to 62.1 ms, and the macromolecules were modeled by 10 line broadened singlets. The amplitude of each of the macromolecule signals was extracted at each TE and fit to a monoexponential function to extract the respective effective T2 values. Absolute quantification of the macromolecule resonances was performed using water signal as a reference. A total of 10 young healthy adult subjects (5 females) were scanned, with spectra being obtained from both the frontal and occipital cortex. Differences in the effective T2 relaxation times and concentrations were investigated between both regions and genders.ResultsA wide disparity was observed between the effective T2 values of the individual resonances; however, no significant differences between gender or region for any of the measured macromolecule concentration or effective T2 values were found.ConclusionThe effective T2 relaxation times and concentration of 10 different macromolecule resonances were measured and found to be well represented by the monoexponential model. These results will be useful for absolute quantification of macromolecules in future studies, or in the generation of synthetic basis sets for optimization or machine learning. Purpose We aimed to investigate the concentration and effective T2 relaxation time of macromolecules assessed with an ultra‐short TE sLASER sequence in 2 brain regions, the occipital and frontal cortex, in both genders at 3T. Methods An optimized sLASER sequence was used in conjunction with a double‐inversion preparation module to null the metabolites. Eight equally spaced TEs were chosen from 20.1 to 62.1 ms, and the macromolecules were modeled by 10 line broadened singlets. The amplitude of each of the macromolecule signals was extracted at each TE and fit to a monoexponential function to extract the respective effective T2 values. Absolute quantification of the macromolecule resonances was performed using water signal as a reference. A total of 10 young healthy adult subjects (5 females) were scanned, with spectra being obtained from both the frontal and occipital cortex. Differences in the effective T2 relaxation times and concentrations were investigated between both regions and genders. Results A wide disparity was observed between the effective T2 values of the individual resonances; however, no significant differences between gender or region for any of the measured macromolecule concentration or effective T2 values were found. Conclusion The effective T2 relaxation times and concentration of 10 different macromolecule resonances were measured and found to be well represented by the monoexponential model. These results will be useful for absolute quantification of macromolecules in future studies, or in the generation of synthetic basis sets for optimization or machine learning. We aimed to investigate the concentration and effective T2 relaxation time of macromolecules assessed with an ultra-short TE sLASER sequence in 2 brain regions, the occipital and frontal cortex, in both genders at 3T.PURPOSEWe aimed to investigate the concentration and effective T2 relaxation time of macromolecules assessed with an ultra-short TE sLASER sequence in 2 brain regions, the occipital and frontal cortex, in both genders at 3T.An optimized sLASER sequence was used in conjunction with a double-inversion preparation module to null the metabolites. Eight equally spaced TEs were chosen from 20.1 to 62.1 ms, and the macromolecules were modeled by 10 line broadened singlets. The amplitude of each of the macromolecule signals was extracted at each TE and fit to a monoexponential function to extract the respective effective T2 values. Absolute quantification of the macromolecule resonances was performed using water signal as a reference. A total of 10 young healthy adult subjects (5 females) were scanned, with spectra being obtained from both the frontal and occipital cortex. Differences in the effective T2 relaxation times and concentrations were investigated between both regions and genders.METHODSAn optimized sLASER sequence was used in conjunction with a double-inversion preparation module to null the metabolites. Eight equally spaced TEs were chosen from 20.1 to 62.1 ms, and the macromolecules were modeled by 10 line broadened singlets. The amplitude of each of the macromolecule signals was extracted at each TE and fit to a monoexponential function to extract the respective effective T2 values. Absolute quantification of the macromolecule resonances was performed using water signal as a reference. A total of 10 young healthy adult subjects (5 females) were scanned, with spectra being obtained from both the frontal and occipital cortex. Differences in the effective T2 relaxation times and concentrations were investigated between both regions and genders.A wide disparity was observed between the effective T2 values of the individual resonances; however, no significant differences between gender or region for any of the measured macromolecule concentration or effective T2 values were found.RESULTSA wide disparity was observed between the effective T2 values of the individual resonances; however, no significant differences between gender or region for any of the measured macromolecule concentration or effective T2 values were found.The effective T2 relaxation times and concentration of 10 different macromolecule resonances were measured and found to be well represented by the monoexponential model. These results will be useful for absolute quantification of macromolecules in future studies, or in the generation of synthetic basis sets for optimization or machine learning.CONCLUSIONThe effective T2 relaxation times and concentration of 10 different macromolecule resonances were measured and found to be well represented by the monoexponential model. These results will be useful for absolute quantification of macromolecules in future studies, or in the generation of synthetic basis sets for optimization or machine learning. |
Author | Gajdošík, Martin Juchem, Christoph Treacy, Michael Landheer, Karl |
Author_xml | – sequence: 1 givenname: Karl orcidid: 0000-0001-5012-3007 surname: Landheer fullname: Landheer, Karl email: kl2968@columbia.edu organization: Columbia University Fu Foundation School of Engineering and Applied Science – sequence: 2 givenname: Martin orcidid: 0000-0003-1570-2825 surname: Gajdošík fullname: Gajdošík, Martin organization: Columbia University Fu Foundation School of Engineering and Applied Science – sequence: 3 givenname: Michael surname: Treacy fullname: Treacy, Michael organization: Columbia University Fu Foundation School of Engineering and Applied Science – sequence: 4 givenname: Christoph orcidid: 0000-0002-1505-201X surname: Juchem fullname: Juchem, Christoph organization: Columbia University College of Physicians and Surgeons |
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We aimed to investigate the concentration and effective T2 relaxation time of macromolecules assessed with an ultra‐short TE sLASER sequence in 2 brain... PurposeWe aimed to investigate the concentration and effective T2 relaxation time of macromolecules assessed with an ultra‐short TE sLASER sequence in 2 brain... We aimed to investigate the concentration and effective T2 relaxation time of macromolecules assessed with an ultra-short TE sLASER sequence in 2 brain... |
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SubjectTerms | Cortex (frontal) Gender Learning algorithms Machine learning Macromolecules magnetic resonance spectroscopy Metabolites Occipital lobe Optimization Relaxation time short TE sLASER |
Title | Concentration and effective T2 relaxation times of macromolecules at 3T |
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