Ebel Andreas, Maudsley Andrew A, Weiner Michael W, Schuff Norbert
Northern California Institute for Research and Education, VA Medical Center San Francisco, San Francisco, CA 94121, USA.
Magn Reson Med. 2005 Sep;54(3):697-701. doi: 10.1002/mrm.20593.
Complete coverage of the in vivo proton metabolite spectrum, including downfield resonances, requires a spectral bandwidth of approximately 9 ppm. Spectral bandwidth of in vivo echo-planar spectroscopic imaging (EPSI) is primarily limited by gradient strength of the oscillating readout gradient, gradient slew rate, and limits on peripheral nerve stimulation for human subjects. Furthermore, conventional EPSI reconstruction, which utilizes even and odd readout echoes separately, makes use of only half the spectral bandwidth. In order to regain full spectral bandwidth in EPSI, it has previously been suggested to apply an interlaced Fourier transform (iFT), which uses even and odd echoes simultaneously. However, this method has not been thoroughly analyzed regarding its usefulness for in vivo 3D EPSI. In this Note, limitations of the iFT method are discussed and an alternative, cyclic spectral unwrapping, is proposed, which is based on prior knowledge of typical in vivo spectral patterns.
要完整覆盖体内质子代谢物谱,包括低场共振,需要约9 ppm的光谱带宽。体内回波平面光谱成像(EPSI)的光谱带宽主要受振荡读出梯度的梯度强度、梯度 slew 率以及人体受试者外周神经刺激限制的影响。此外,传统的EPSI重建分别利用偶数和奇数读出回波,仅使用了一半的光谱带宽。为了在EPSI中恢复全光谱带宽,此前有人建议应用交错傅里叶变换(iFT),它同时使用偶数和奇数回波。然而,关于该方法在体内3D EPSI中的实用性尚未进行深入分析。在本笔记中,讨论了iFT方法的局限性,并提出了一种基于典型体内光谱模式先验知识的替代方法——循环光谱展开。