Young Richard, Serrai Hacene
Institute for Biodiagnostics (IBD), National Research Council, Winnipeg, MB, Canada.
Magn Reson Med. 2009 Jan;61(1):6-15. doi: 10.1002/mrm.21756.
We have recently proposed a two-dimensional Wavelet Encoding-Spectroscopic Imaging (WE-SI) technique as an alternative to Chemical Shift Imaging (CSI), to reduce acquisition time and crossvoxel contamination in magnetic resonance spectroscopic imaging (MRSI). In this article we describe the extension of the WE-SI technique to three dimensions and its implementation on a clinical 1.5 T General Electric (GE) scanner. Phantom and in vivo studies are carried out to demonstrate the usefulness of this technique for further acquisition time reduction with low voxel contamination. In wavelet encoding, a set of dilated and translated prototype functions called wavelets are used to span a localized space by dividing it into a set of subspaces with predetermined sizes and locations. In spectroscopic imaging, this process is achieved using radiofrequency (RF) pulses with profiles resembling the wavelet shapes. Slice selective excitation and refocusing RF pulses, with single-band and dual-band profiles similar to Haar wavelets, are used in a modified PRESS sequence to acquire 3D WE-SI data. Wavelet dilation and translation are achieved by changing the strength of the localization gradients and frequency shift of the RF pulses, respectively. The desired spatial resolution in each direction sets the corresponding number of dilations (increases in the localization gradients), and consequently, the number of translations (frequency shift) of the Haar wavelets (RF pulses), which are used to collect magnetic resonance (MR) signals from the corresponding subspaces. Data acquisition time is reduced by using the minimum recovery time (TR(min)), also called effective time, when successive MR signals from adjacent subspaces are collected. Inverse wavelet transform is performed on the acquired data to produce metabolite maps. The proposed WE-SI method is compared in terms of acquisition time, pixel bleed, and signal-to-noise ratio to the CSI technique. The study outcome shows that 3D WE-SI provides accurate results while reducing both acquisition time and voxel contamination.
我们最近提出了一种二维小波编码光谱成像(WE-SI)技术,作为化学位移成像(CSI)的替代方法,以减少磁共振波谱成像(MRSI)中的采集时间和体素间污染。在本文中,我们描述了将WE-SI技术扩展到三维及其在临床1.5 T通用电气(GE)扫描仪上的实现。进行了体模和体内研究,以证明该技术在进一步减少采集时间和降低体素污染方面的有用性。在小波编码中,一组称为小波的扩张和平移原型函数通过将局部空间划分为一组具有预定大小和位置的子空间来跨越该局部空间。在光谱成像中,这个过程是通过使用具有类似于小波形状的轮廓的射频(RF)脉冲来实现的。在改进的PRESS序列中,使用具有类似于哈尔小波的单波段和双波段轮廓的切片选择性激发和重聚焦RF脉冲来采集3D WE-SI数据。小波扩张和平移分别通过改变定位梯度的强度和RF脉冲的频率偏移来实现。每个方向上所需的空间分辨率设置了相应的扩张次数(定位梯度增加),从而设置了用于从相应子空间收集磁共振(MR)信号的哈尔小波(RF脉冲)的平移次数(频率偏移)。通过使用最小恢复时间(TR(min)),也称为有效时间,当从相邻子空间收集连续的MR信号时,采集时间得以减少。对采集到的数据进行小波逆变换以生成代谢物图谱。将所提出的WE-SI方法在采集时间、像素混叠和信噪比方面与CSI技术进行了比较。研究结果表明,3D WE-SI在减少采集时间和体素污染的同时提供了准确的结果。