Advanced Imaging Research Center, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA.
Magn Reson Med. 2009 Nov;62(5):1305-10. doi: 10.1002/mrm.22125.
Measurement of glycine in human frontal brain by an optimized point-resolved spectroscopy sequence at 7 T is reported. Echo time dependencies of the overlapping coupled resonances of myo-inositol, free choline, and threonine were investigated with density matrix simulations, incorporating the slice-selective radiofrequency and gradient pulses. The numerical simulations indicated that the selectivity of the 3.55-ppm glycine singlet is maximized at (TE(1), TE(2)) = (101, 51) ms. Phantom experiments indicated that the myo-inositol peak amplitude between 3.5 and 3.6 ppm is reduced by a factor of 30 following the optimized point-resolved spectroscopy, as predicted by the simulation. From LCModel analyses, the glycine concentration in the medial prefrontal cortex in healthy adults was estimated, with a mean Cramér-Rao lower bound of 7 +/- 1% (mean +/- standard deviation; n = 7), to be 0.8 +/- 0.1 mM, with reference to total creatine at 8 mM.
报道了在 7T 下通过优化的点分辨波谱序列测量人额叶脑内甘氨酸的方法。采用密度矩阵模拟方法,结合片选射频和梯度脉冲,研究了肌醇、游离胆碱和苏氨酸重叠偶合共振的回波时间依赖性。数值模拟表明,3.55ppm 甘氨酸单峰的选择性在(TE(1),TE(2))=(101,51)ms 时达到最大值。在体实验表明,优化的点分辨波谱后,3.5 到 3.6ppm 之间的肌醇峰幅度降低了 30 倍,这与模拟结果一致。通过 LCModel 分析,对健康成年人的内侧前额叶皮质中的甘氨酸浓度进行了估计,以 8mM 总肌酸为参照,甘氨酸浓度的平均 Cramér-Rao 下限为 7% +/- 1%(平均值 +/- 标准差;n=7),为 0.8 +/- 0.1mM。