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Comparison of 1.5T and 3T (1)H MR Spectroscopy for Human Brain Tumors

OBJECTIVE: We wanted to estimate the practical improvements of 3T proton MR spectroscopy ((1)H MRS) as compared with 1.5T (1)H MRS for the evaluation of human brain tumors. MATERIALS AND METHODS: Single voxel (1)H MRS was performed at both 1.5T and 3T in 13 patients suffering with brain tumors. Usin...

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Autores principales: Kim, Ji-hoon, Chang, Kee-Hyun, Na, Dong Gyu, Song, In Chan, Kim, Seung Ja, Kwon, Bae Ju, Han, Moon Hee
Formato: Texto
Lenguaje:English
Publicado: The Korean Radiological Society 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2667596/
https://www.ncbi.nlm.nih.gov/pubmed/16969044
http://dx.doi.org/10.3348/kjr.2006.7.3.156
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author Kim, Ji-hoon
Chang, Kee-Hyun
Na, Dong Gyu
Song, In Chan
Kim, Seung Ja
Kwon, Bae Ju
Han, Moon Hee
author_facet Kim, Ji-hoon
Chang, Kee-Hyun
Na, Dong Gyu
Song, In Chan
Kim, Seung Ja
Kwon, Bae Ju
Han, Moon Hee
author_sort Kim, Ji-hoon
collection PubMed
description OBJECTIVE: We wanted to estimate the practical improvements of 3T proton MR spectroscopy ((1)H MRS) as compared with 1.5T (1)H MRS for the evaluation of human brain tumors. MATERIALS AND METHODS: Single voxel (1)H MRS was performed at both 1.5T and 3T in 13 patients suffering with brain tumors. Using the same data acquisition parameters at both field strengths, the (1)H MRS spectra were obtained with a short echo time (TE) (35 msec) and an intermediate TE (144 msec) with the voxel size ranging from 2.0 cm(3) to 8.7 cm(3). The signal to noise ratios (SNRs) of the metabolites (myoinositol [MI], choline compounds [Cho], creatine/phosphocreatine [Cr], N-acetyl-aspartate [NAA], lipid and lactate [LL]) and the metabolite ratios of MI/Cr, Cho/Cr, Cho/NAA and LL/Cr were compared at both TEs between the two field strengths in each brain tumor. The degrees of spectral resolution between the Cho and Cr peaks were qualitatively compared between the two field strengths in each brain tumor. RESULTS: The SNRs of the metabolites at 3T demonstrated 49-73% increase at a short TE (p < 0.01) and only 2-12% increase at an intermediate TE (p > 0.05) compared with those of 1.5T. The SNR of inverted lactate at an intermediate TE decreased down to 49% with poorer inversion at 3T (p < 0.05). There was no significant difference in the metabolite ratios between the two field strengths. The degrees of the spectral resolution at 3T were slightly superior to those of 1.5T at a short TE. CONCLUSION: As compared with 1.5T, 3T (1)H MRS demonstrated 49-73% SNR increase in the cerebral metabolites and slightly superior spectral resolution only at a short TE, but little at an intermediate TE, in the brain tumors. There was no significant difference in the metabolite ratios between the two field strengths.
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spelling pubmed-26675962009-04-22 Comparison of 1.5T and 3T (1)H MR Spectroscopy for Human Brain Tumors Kim, Ji-hoon Chang, Kee-Hyun Na, Dong Gyu Song, In Chan Kim, Seung Ja Kwon, Bae Ju Han, Moon Hee Korean J Radiol Original Article OBJECTIVE: We wanted to estimate the practical improvements of 3T proton MR spectroscopy ((1)H MRS) as compared with 1.5T (1)H MRS for the evaluation of human brain tumors. MATERIALS AND METHODS: Single voxel (1)H MRS was performed at both 1.5T and 3T in 13 patients suffering with brain tumors. Using the same data acquisition parameters at both field strengths, the (1)H MRS spectra were obtained with a short echo time (TE) (35 msec) and an intermediate TE (144 msec) with the voxel size ranging from 2.0 cm(3) to 8.7 cm(3). The signal to noise ratios (SNRs) of the metabolites (myoinositol [MI], choline compounds [Cho], creatine/phosphocreatine [Cr], N-acetyl-aspartate [NAA], lipid and lactate [LL]) and the metabolite ratios of MI/Cr, Cho/Cr, Cho/NAA and LL/Cr were compared at both TEs between the two field strengths in each brain tumor. The degrees of spectral resolution between the Cho and Cr peaks were qualitatively compared between the two field strengths in each brain tumor. RESULTS: The SNRs of the metabolites at 3T demonstrated 49-73% increase at a short TE (p < 0.01) and only 2-12% increase at an intermediate TE (p > 0.05) compared with those of 1.5T. The SNR of inverted lactate at an intermediate TE decreased down to 49% with poorer inversion at 3T (p < 0.05). There was no significant difference in the metabolite ratios between the two field strengths. The degrees of the spectral resolution at 3T were slightly superior to those of 1.5T at a short TE. CONCLUSION: As compared with 1.5T, 3T (1)H MRS demonstrated 49-73% SNR increase in the cerebral metabolites and slightly superior spectral resolution only at a short TE, but little at an intermediate TE, in the brain tumors. There was no significant difference in the metabolite ratios between the two field strengths. The Korean Radiological Society 2006 2006-09-30 /pmc/articles/PMC2667596/ /pubmed/16969044 http://dx.doi.org/10.3348/kjr.2006.7.3.156 Text en Copyright © 2006 The Korean Radiological Society http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Kim, Ji-hoon
Chang, Kee-Hyun
Na, Dong Gyu
Song, In Chan
Kim, Seung Ja
Kwon, Bae Ju
Han, Moon Hee
Comparison of 1.5T and 3T (1)H MR Spectroscopy for Human Brain Tumors
title Comparison of 1.5T and 3T (1)H MR Spectroscopy for Human Brain Tumors
title_full Comparison of 1.5T and 3T (1)H MR Spectroscopy for Human Brain Tumors
title_fullStr Comparison of 1.5T and 3T (1)H MR Spectroscopy for Human Brain Tumors
title_full_unstemmed Comparison of 1.5T and 3T (1)H MR Spectroscopy for Human Brain Tumors
title_short Comparison of 1.5T and 3T (1)H MR Spectroscopy for Human Brain Tumors
title_sort comparison of 1.5t and 3t (1)h mr spectroscopy for human brain tumors
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2667596/
https://www.ncbi.nlm.nih.gov/pubmed/16969044
http://dx.doi.org/10.3348/kjr.2006.7.3.156
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