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本文引用的文献

1
Non-invasive detection of glycine as a biomarker of malignancy in childhood brain tumours using in-vivo 1H MRS at 1.5 tesla confirmed by ex-vivo high-resolution magic-angle spinning NMR.采用 1.5 特斯拉体内 1H MRS 对儿童脑肿瘤进行非侵入性甘氨酸生物标志物检测,经离体高分辨率魔角旋转 NMR 证实。
NMR Biomed. 2010 Jan;23(1):80-7. doi: 10.1002/nbm.1432.
2
Measurement of glycine in human prefrontal brain by point-resolved spectroscopy at 7.0 tesla in vivo.在 7.0 特斯拉活体中通过点分辨光谱法测量人前额叶脑内的甘氨酸。
Magn Reson Med. 2009 Nov;62(5):1305-10. doi: 10.1002/mrm.22125.
3
In vivo 1H NMR spectroscopy of the human brain at high magnetic fields: metabolite quantification at 4T vs. 7T.高磁场下人脑的体内 1H NMR 波谱学:4T 与 7T 下代谢产物定量分析。
Magn Reson Med. 2009 Oct;62(4):868-79. doi: 10.1002/mrm.22086.
4
Oral glycine administration increases brain glycine/creatine ratios in men: a proton magnetic resonance spectroscopy study.口服甘氨酸可提高男性大脑中的甘氨酸/肌酸比率:一项质子磁共振波谱研究。
Psychiatry Res. 2009 Aug 30;173(2):143-9. doi: 10.1016/j.pscychresns.2009.03.004. Epub 2009 Jun 24.
5
In vivo measurement of glycine with short echo-time 1H MRS in human brain at 7 T.在7T磁场下,采用短回波时间1H磁共振波谱对人脑内甘氨酸进行活体测量。
MAGMA. 2009 Feb;22(1):1-4. doi: 10.1007/s10334-008-0152-0. Epub 2008 Oct 24.
6
1H MR spectroscopic imaging with short and long echo time to discriminate glycine in glial tumours.采用短回波时间和长回波时间的1H磁共振波谱成像鉴别胶质肿瘤中的甘氨酸。
MAGMA. 2009 Feb;22(1):33-41. doi: 10.1007/s10334-008-0145-z. Epub 2008 Oct 1.
7
Numerical simulations of localized high field 1H MR spectroscopy.局部高场1H磁共振波谱的数值模拟。
J Magn Reson. 2008 Nov;195(1):67-75. doi: 10.1016/j.jmr.2008.08.010. Epub 2008 Aug 28.
8
Editing through multiple bonds: threonine detection.通过多键进行编辑:苏氨酸检测
Magn Reson Med. 2008 Feb;59(2):245-51. doi: 10.1002/mrm.21492.
9
Measurement of glycine in human brain by triple refocusing 1H-MRS in vivo at 3.0T.在3.0T场强下通过体内三重聚焦1H磁共振波谱法测量人脑中的甘氨酸。
Magn Reson Med. 2008 Jan;59(1):59-64. doi: 10.1002/mrm.21450.
10
Central neurocytoma: typical magnetic resonance spectroscopy findings and atypical ventricular dissemination.中枢神经细胞瘤:典型的磁共振波谱表现及不典型的脑室播散
Magn Reson Imaging. 2008 Jan;26(1):59-64. doi: 10.1016/j.mri.2007.04.005. Epub 2007 Jun 18.

在 3T 场强下通过 1H-MRS 对人脑内甘氨酸进行测量:在脑肿瘤中的应用。

Measurement of glycine in the human brain in vivo by 1H-MRS at 3 T: application in brain tumors.

机构信息

Advanced Imaging Research Center, University of Texas Southwestern Medical Center, Dallas, Texas, USA.

出版信息

Magn Reson Med. 2011 Sep;66(3):609-18. doi: 10.1002/mrm.22857. Epub 2011 Mar 9.

DOI:10.1002/mrm.22857
PMID:21394775
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3139742/
Abstract

Glycine is a key metabolic intermediate required for the synthesis of proteins, nucleic acids, and other molecules, and its detection in cancer could, therefore, provide biologically relevant information about the growth of the tumor. Here, we report measurement of glycine in human brain and gliomas by an optimized point-resolved spectroscopy sequence at 3 T. Echo time dependence of the major obstacle, myo-inositol (mI) multiplet, was investigated with numerical simulations, incorporating the 3D volume localization. The simulations indicated that a subecho pair (TE(1) , TE(2) ) = (60, 100) ms permits detection of both glycine and mI with optimum selectivity. In vivo validation of the optimized point-resolved spectroscopy was conducted on the right parietal cortex of five healthy volunteers. Metabolite signals estimated from LC Model were normalized with respect to the brain water signal, and the concentrations were evaluated assuming the total creatine concentration at 8 mM. The glycine concentration was estimated as 0.6 ± 0.1 mM (mean ± SD, n = 5), with a mean Cramér-Rao lower bound of 9 ± 1%. The point-resolved spectroscopy sequence was applied to measure the glycine levels in patients with glioblastoma multiforme. Metabolite concentrations were obtained using the water signal from the tumor mass. The study revealed that a subset of human gliomas contains glycine levels elevated 1.5-8 fold relative to normal.

摘要

甘氨酸是合成蛋白质、核酸和其他分子所需的关键代谢中间产物,因此,在癌症中检测到甘氨酸可以提供关于肿瘤生长的生物学相关信息。在这里,我们报告了在 3T 下通过优化的点分辨波谱序列测量人脑中甘氨酸和神经胶质瘤的情况。通过数值模拟研究了主要障碍肌醇(mI)多重峰的回波时间依赖性,模拟结果表明,亚回波对(TE(1),TE(2))=(60,100)ms 可以最佳选择性地检测甘氨酸和 mI。在五名健康志愿者的右顶叶皮层上对优化的点分辨波谱进行了体内验证。使用 LC Model 从 LC Model 估计的代谢物信号相对于脑水信号进行了归一化,并假设总肌酸浓度为 8 mM 来评估浓度。甘氨酸浓度估计为 0.6 ± 0.1 mM(平均值 ± SD,n = 5),平均克拉默-罗下限为 9 ± 1%。点分辨波谱序列用于测量多形性胶质母细胞瘤患者的甘氨酸水平。使用肿瘤质量的水信号获得代谢物浓度。研究表明,一部分人类神经胶质瘤的甘氨酸水平比正常水平升高了 1.5-8 倍。