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Dynamic (1)H-MRS assessment of brain tumors: A novel approach for differential diagnosis of glioma

PURPOSE: To determine whether the changes of [Cho/NAA] ratio in patients with glioma, measured by dynamic (1)H-MRS can be used to differentiate between high-grade and low-grade gliomas. MATERIALS AND METHODS: This prospective study was approved by the institutional ethics committee. Written informed...

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Autores principales: Tong, Tong, Yang, Zhong, Chen, John W., Zhu, Jianming, Yao, Zhenwei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4741675/
https://www.ncbi.nlm.nih.gov/pubmed/26337080
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author Tong, Tong
Yang, Zhong
Chen, John W.
Zhu, Jianming
Yao, Zhenwei
author_facet Tong, Tong
Yang, Zhong
Chen, John W.
Zhu, Jianming
Yao, Zhenwei
author_sort Tong, Tong
collection PubMed
description PURPOSE: To determine whether the changes of [Cho/NAA] ratio in patients with glioma, measured by dynamic (1)H-MRS can be used to differentiate between high-grade and low-grade gliomas. MATERIALS AND METHODS: This prospective study was approved by the institutional ethics committee. Written informed consent was obtained. Forty-nine patients with biopsy-proven glioma and 20 normal control subjects were recruited in this study. The maximum [Cho/NAA] ratios, acquired at 0 min, and at 6 min, were calculated and assessed from volume of interests (VOI) in the tumor areas and in the surrounding normal tissue for each patient. Absolute difference in the [Cho/NAA] ratios, from MRS acquired at 0 and 6 min, in high-grade glioma, low-grade glioma, and control subjects were compared. RESULTS: The maximum [Cho/NAA] ratio acquired from the tumor area at the 0 min is 6.08 ± 2.02, which was significantly different (p = .017) from that acquired after 6 min, 4.87 ± 2.13. The [Cho/NAA] ratio from the surrounding normal tissue area did not change significantly from spectra acquired at different times (0 min, 6 min). Absolute difference in [Cho/NAA] ratios acquired at 0 and 6 min time points were significantly higher (P < 0.001) in high-grade glioma (= 3.86 ± 3.31) than in low-grade glioma (= 0.81 ± 0.90), and control subjects (0.061 ± 0.026, P = 0.000), while there was no significantly difference in low-grade glioma and control subjects. CONCLUSIONS: Dynamic (1)H-MRS can be useful for differential diagnosis between high-grade and low-grade gliomas as well as insight into the heterogeneity within the tumor.
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spelling pubmed-47416752016-03-03 Dynamic (1)H-MRS assessment of brain tumors: A novel approach for differential diagnosis of glioma Tong, Tong Yang, Zhong Chen, John W. Zhu, Jianming Yao, Zhenwei Oncotarget Clinical Research Paper PURPOSE: To determine whether the changes of [Cho/NAA] ratio in patients with glioma, measured by dynamic (1)H-MRS can be used to differentiate between high-grade and low-grade gliomas. MATERIALS AND METHODS: This prospective study was approved by the institutional ethics committee. Written informed consent was obtained. Forty-nine patients with biopsy-proven glioma and 20 normal control subjects were recruited in this study. The maximum [Cho/NAA] ratios, acquired at 0 min, and at 6 min, were calculated and assessed from volume of interests (VOI) in the tumor areas and in the surrounding normal tissue for each patient. Absolute difference in the [Cho/NAA] ratios, from MRS acquired at 0 and 6 min, in high-grade glioma, low-grade glioma, and control subjects were compared. RESULTS: The maximum [Cho/NAA] ratio acquired from the tumor area at the 0 min is 6.08 ± 2.02, which was significantly different (p = .017) from that acquired after 6 min, 4.87 ± 2.13. The [Cho/NAA] ratio from the surrounding normal tissue area did not change significantly from spectra acquired at different times (0 min, 6 min). Absolute difference in [Cho/NAA] ratios acquired at 0 and 6 min time points were significantly higher (P < 0.001) in high-grade glioma (= 3.86 ± 3.31) than in low-grade glioma (= 0.81 ± 0.90), and control subjects (0.061 ± 0.026, P = 0.000), while there was no significantly difference in low-grade glioma and control subjects. CONCLUSIONS: Dynamic (1)H-MRS can be useful for differential diagnosis between high-grade and low-grade gliomas as well as insight into the heterogeneity within the tumor. Impact Journals LLC 2015-08-20 /pmc/articles/PMC4741675/ /pubmed/26337080 Text en Copyright: © 2015 Tong et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Clinical Research Paper
Tong, Tong
Yang, Zhong
Chen, John W.
Zhu, Jianming
Yao, Zhenwei
Dynamic (1)H-MRS assessment of brain tumors: A novel approach for differential diagnosis of glioma
title Dynamic (1)H-MRS assessment of brain tumors: A novel approach for differential diagnosis of glioma
title_full Dynamic (1)H-MRS assessment of brain tumors: A novel approach for differential diagnosis of glioma
title_fullStr Dynamic (1)H-MRS assessment of brain tumors: A novel approach for differential diagnosis of glioma
title_full_unstemmed Dynamic (1)H-MRS assessment of brain tumors: A novel approach for differential diagnosis of glioma
title_short Dynamic (1)H-MRS assessment of brain tumors: A novel approach for differential diagnosis of glioma
title_sort dynamic (1)h-mrs assessment of brain tumors: a novel approach for differential diagnosis of glioma
topic Clinical Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4741675/
https://www.ncbi.nlm.nih.gov/pubmed/26337080
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