High-quality lipid suppression and B0 shimming for human brain 1H MRSI

IF 4.7 2区 医学 Q1 NEUROIMAGING
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引用次数: 0

Abstract

Magnetic Resonance Spectroscopic Imaging (MRSI) is a powerful technique that can map the metabolic profile in the brain non-invasively. Extracranial lipid contamination and insufficient B0 homogeneity however hampers robustness, and as a result has hindered widespread use of MRSI in clinical and research settings. Over the last six years we have developed highly effective extracranial lipid suppression methods with a second order gradient insert (ECLIPSE) utilizing inner volume selection (IVS) and outer volume suppression (OVS) methods. While ECLIPSE provides > 100-fold in lipid suppression with modest radio frequency (RF) power requirements and immunity to B1+ field variations, axial coverage is reduced for non-elliptical head shapes. In this work we detail the design, construction, and utility of MC-ECLIPSE, a pulsed second order gradient coil with Z2 and X2Y2 fields, combined with a 54-channel multi-coil (MC) array. The MC-ECLIPSE platform allows arbitrary region of interest (ROI) shaped OVS for full-axial slice coverage, in addition to MC-based B0 field shimming, for robust human brain proton MRSI.

In vivo experiments demonstrate that MC-ECLIPSE allows axial brain coverage of 92–95 % is achieved following arbitrary ROI shaped OVS for various head shapes. The standard deviation (SD) of the residual B0 field following SH2 and MC shimming were 25 ± 9 Hz and 18 ± 8 Hz over a 5 cm slab, and 18 ± 5 Hz and 14 ± 6 Hz over a 1.5 cm slab, respectively. These results demonstrate that B0 magnetic field shimming with the MC array supersedes second order harmonic capabilities available on standard MRI systems for both restricted and large ROIs. Furthermore, MC based B0 shimming provides comparable shimming performance to an unrestricted SH5 shim set for both restricted, and 5-cm slab shim challenges.

Phantom experiments demonstrate the high level of localization performance achievable with MC-ECLIPSE, with ROI edge chemical shift displacements ranging from 1–3 mm with a median value of 2 mm, and transition width metrics ranging from 1–2.5 mm throughout the ROI edge. Furthermore, MC based B0 shimming is comparable to performance following a full set of unrestricted spherical harmonic fields up to order 5. Short echo time MRSI and GABA-edited MRSI acquisitions in the human brain following MC-shimming and arbitrary ROI shaping demonstrate full-axial slice coverage and extracranial lipid artifact free spectra. MC-ECLIPSE allows full-axial coverage and robust MRSI acquisitions, while allowing interrogation of cortical tissue proximal to the skull, which has significant value in a wide range of neurological and psychiatric conditions.

磁共振波谱成像(MRSI)是一项功能强大的技术,可以无创绘制大脑的代谢图谱。然而,颅外脂质污染和 B0 不够均匀阻碍了 MRSI 的稳健性,因此阻碍了 MRSI 在临床和研究环境中的广泛应用。在过去的六年中,我们利用内体积选择(IVS)和外体积抑制(OVS)方法,开发出了高效的颅外脂质抑制方法,该方法具有二阶梯度插入(ECLIPSE)。虽然 ECLIPSE 能以适度的射频(RF)功率要求和对 B1+ 场变化的免疫力实现 100 倍的脂质抑制,但对于非椭圆形头型,其轴向覆盖范围会减小。在这项工作中,我们详细介绍了 MC-ECLIPSE 的设计、构造和实用性,它是一个具有 Z2 和 X2Y2 场的脉冲二阶梯度线圈,与 54 通道多线圈 (MC) 阵列相结合。MC-ECLIPSE 平台可通过任意感兴趣区(ROI)形状的 OVS 实现全轴向切片覆盖,此外还可进行基于 MC 的 B0 场修整,从而实现稳健的人脑质子 MRSI。体内实验证明,MC-ECLIPSE 可在各种头型的任意感兴趣区形状的 OVS 之后实现 92-95% 的轴向脑覆盖率。SH2和MC修整后残余B0磁场的标准偏差(SD)在5厘米平板上分别为25±9赫兹和18±8赫兹,在1.5厘米平板上分别为18±5赫兹和14±6赫兹。这些结果表明,使用 MC 阵列进行的 B0 磁场微调超越了标准磁共振成像系统对受限和大型 ROI 的二阶谐波能力。Phantom 实验证明了 MC-ECLIPSE 可实现的高水平定位性能,ROI 边缘化学位移位移范围为 1-3 毫米,中值为 2 毫米,整个 ROI 边缘的过渡宽度指标范围为 1-2.5 毫米。此外,基于 MC 的 B0 shimming 与全套无限制球形谐波场的性能相当,最高可达 5 阶。在 MC-shimming和任意ROI整形后进行的人脑短回波时间MRSI和GABA编辑MRSI采集显示了全轴向切片覆盖和无颅外脂质伪影光谱。MC-ECLIPSE 允许进行全轴覆盖和稳健的 MRSI 采集,同时允许对颅骨近端皮质组织进行检查,这对各种神经和精神疾病具有重要价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
NeuroImage
NeuroImage 医学-核医学
CiteScore
11.30
自引率
10.50%
发文量
809
审稿时长
63 days
期刊介绍: NeuroImage, a Journal of Brain Function provides a vehicle for communicating important advances in acquiring, analyzing, and modelling neuroimaging data and in applying these techniques to the study of structure-function and brain-behavior relationships. Though the emphasis is on the macroscopic level of human brain organization, meso-and microscopic neuroimaging across all species will be considered if informative for understanding the aforementioned relationships.
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