Russell H. Morgan Department of Radiology and Radiological Science, The Johns Hopkins University, Baltimore, Maryland 21202, USA.
Magn Reson Med. 2011 Jun;65(6):1509-14. doi: 10.1002/mrm.22747. Epub 2011 Feb 17.
There is increasing interest in the J-PRESS technique, an in vivo implementation of two-dimensional J-spectroscopy combined with PRESS localization, for high-field spectroscopy studies of the human brain. The experiment is designed to resolve scalar couplings in the second, indirectly detected dimension, but will only do so if the slice-selective refocusing pulses in the PRESS sequence affect all coupled spins equally. At high magnet field strengths, due to limited RF pulse bandwidth, PRESS-based localization results in spatially dependent evolution of coupling. In some regions of the localized volume, coupling evolves during the PRESS echo time, while in other regions it may be partially or fully refocused. This study investigates the impact of this effect on the appearance of the J-PRESS spectrum for coupled spins, focusing on two commonly observed metabolites, lactate and N-acetyl aspartate, showing that such behavior results in additional peaks in the J-resolved spectrum (termed J-refocused peaks). It is also demonstrated that increasing the bandwidth of refocusing pulses significantly reduces the size of such signals.
人们对 J-PRESS 技术越来越感兴趣,这是一种将二维 J 谱与 PRESS 定位相结合的活体实施方法,用于研究人类大脑的高场光谱。该实验旨在解析第二维(间接检测)中的标量耦合,但只有在 PRESS 序列中的切片选择性重聚焦脉冲对所有耦合自旋产生相同影响的情况下才能实现。在高磁场强度下,由于 RF 脉冲带宽有限,基于 PRESS 的定位会导致耦合的空间相关演化。在局部化体积的某些区域中,耦合在 PRESS 回波时间期间演化,而在其他区域中,它可能部分或完全重聚焦。本研究调查了这种效应对耦合自旋的 J-PRESS 光谱外观的影响,重点关注两种常见的代谢物,即乳酸盐和 N-乙酰天冬氨酸,表明这种行为会导致 J 分辨光谱中出现额外的峰(称为 J 重聚焦峰)。还证明,增加重聚焦脉冲的带宽会显著减小这些信号的大小。