Department of Physics, University of Alberta, Edmonton, Alta, Canada.
J Magn Reson. 2010 Mar;203(1):66-72. doi: 10.1016/j.jmr.2009.12.002. Epub 2009 Dec 4.
An optimization of the PRESS sequence for magnetic resonance spectroscopy is presented to simultaneously detect the important brain metabolites of glutamate (Glu) and glutamine (Gln) at field strengths of 1.5, 3, 4.7, and 7T. Standard, clinical examinations typically use short echo times which in general are not ideal for the separation of Glu and Gln. The optimization procedure is based on numerical product operator simulations to produce yield and overlap measurements for all possible practical choices of PRESS inter-echo timings. The simulations illustrate the substantial modulations in Glu and Gln with field strength. At all field strengths, the optimized timings demonstrate a significant reduction in overlap compared to short echo PRESS, while maintaining a high metabolite signal, with Glu and Gln yields >90% when excluding T2 relaxation losses. Minimal overlap was attained at 7T (0.3% Gln contamination in the Glu signal), and 4.7T (1.2%). The optimized timings were applied in vivo on healthy volunteers at field strengths of 1.5 and 4.7T.
本文提出了一种 PRESS 序列的优化方法,可在 1.5、3、4.7 和 7T 场强下同时检测谷氨酸(Glu)和谷氨酰胺(Gln)等重要脑代谢物。标准的临床检查通常使用短回波时间,但一般来说,这种时间并不适合 Glu 和 Gln 的分离。优化过程基于数值乘积算子模拟,针对所有可能的 PRESS 回波间隔的实际选择,生成产率和重叠测量值。模拟结果表明,随着场强的增加,Glu 和 Gln 的变化很大。在所有场强下,与短回波 PRESS 相比,优化后的时间间隔显著降低了重叠,同时保持了较高的代谢物信号,当排除 T2 弛豫损耗时,Glu 和 Gln 的产率>90%。在 7T 时(Glu 信号中 Gln 污染 0.3%)和 4.7T 时(1.2%)达到最小重叠。优化后的时间间隔应用于 1.5 和 4.7T 场强下的健康志愿者的体内研究。