CREATIS CNRS UMR 5220 Inserm U1044, Université de Lyon 1, Université de Lyon, Lyon, France.
J Magn Reson. 2012 Feb;215:50-5. doi: 10.1016/j.jmr.2011.12.013. Epub 2011 Dec 23.
2D Magnetic Resonance Spectroscopy (MRS) is a well known tool for the analysis of complicated and overlapped MR spectra and was therefore originally used for structural analysis. It also presents a potential for biomedical applications as shown by an increasing number of works related to localized in vivo experiments. However, 2D MRS suffers from long acquisition times due to the necessary collection of numerous increments in the indirect dimension (t(1)). This paper presents the first 3D localized 2D ultrafast J-resolved MRS sequence, developed on a small animal imaging system, allowing the acquisition of a 3D localized 2D J-resolved MRS spectrum in a single scan. Sequence parameters were optimized regarding Signal-to-Noise ratio and spectral resolution. Sensitivity and spatial localization properties were characterized and discussed. An automatic post-processing method allowing the reduction of artifacts inherent to ultrafast excitation is also presented. This sequence offers an efficient signal localization and shows a great potential for in vivo dynamic spectroscopy.
2D 磁共振波谱(MRS)是分析复杂和重叠的磁共振谱的一种常用工具,因此最初用于结构分析。它也具有生物医学应用的潜力,越来越多与局部活体实验相关的工作表明了这一点。然而,2D MRS 由于在间接维度(t(1))上必须采集大量增量,因此采集时间较长。本文介绍了首个基于小动物成像系统开发的 3D 局部化 2D 超快 J 分辨 MRS 序列,可在单次扫描中采集 3D 局部化 2D J 分辨 MRS 谱。序列参数针对信噪比和光谱分辨率进行了优化。对灵敏度和空间定位特性进行了表征和讨论。还提出了一种自动后处理方法,可减少超快激发固有的伪影。该序列提供了有效的信号定位,并显示出在体内动态光谱学中的巨大潜力。