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基于双读出的 EPI-J 分辨波谱成像:人脑代谢物的实现与定量。

Echo-Planar J-resolved Spectroscopic Imaging using Dual Read-outs: Implementation and Quantitation of Human Brain Metabolites.

机构信息

Department of Radiological Sciences, David Geffen School of Medicine at UCLA, Los Angeles, California, USA.

UCLA School of Nursing, Los Angeles, California, USA.

出版信息

Sci Rep. 2017 Jun 8;7(1):3087. doi: 10.1038/s41598-017-03121-0.

Abstract

Attempts have been made to reduce the total scan time in multi-dimensional J-resolved spectroscopic imaging (JRESI) using an echo-planar (EP) readout gradient, but acquisition duration remains a limitation for routine clinical use in the brain. We present here a significant acceleration achieved with a 4D EP-JRESI sequence that collects dual phase encoded lines within a single repetition time (TR) using two bipolar read-out trains. The performance and reliability of this novel 4D sequence, called Multi-Echo based Echo-Planar J-resolved Spectroscopic Imaging (ME-EP-JRESI), was evaluated in 10 healthy controls and a brain phantom using a 3 T MRI/MRS scanner. The prior knowledge fitting (ProFit) algorithm, with a new simulated basis set consisting of macromolecules and lipids apart from metabolites of interest, was used for quantitation. Both phantom and in-vivo data demonstrated that localization and spatial/spectral profiles of metabolites from the ME-EP-JRESI sequence were in good agreement with that of the EP-JRESI sequence. Both in the occipital and temporal lobe, metabolites with higher physiological concentrations including Glx (Glu+Gln), tNAA (NAA+NAAG), mI all had coefficient of variations between 9-25%. In summary, we have implemented, validated and tested the ME-EP-JRESI sequence, demonstrating that multi-echo acquisition can successfully reduce the total scan duration for EP-JRESI sequences.

摘要

已经尝试使用回波平面(EP)读出梯度来减少多维 J 分辨波谱成像(JRESI)中的总扫描时间,但采集时间仍然是大脑常规临床应用的一个限制。我们在此介绍了一种使用双极读出列车在单个重复时间(TR)内收集双相位编码线的 4D EP-JRESI 序列实现的显著加速。这种称为基于多回波的 EP-JRESI(ME-EP-JRESI)的新型 4D 序列的性能和可靠性在 10 名健康对照者和脑部体模上使用 3T MRI/MRS 扫描仪进行了评估。先前知识拟合(ProFit)算法,使用除感兴趣代谢物之外的大分子和脂质组成的新模拟基础集,用于定量。体模和体内数据均表明,ME-EP-JRESI 序列的代谢物的定位和空间/光谱分布与 EP-JRESI 序列吻合良好。在枕叶和颞叶中,具有较高生理浓度的代谢物,包括 Glx(Glu+Gln)、tNAA(NAA+NAAG)、mI 的变异系数均在 9-25%之间。总之,我们已经实施、验证和测试了 ME-EP-JRESI 序列,证明了多回波采集可以成功地减少 EP-JRESI 序列的总扫描时间。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e9b/5465060/28bd1616f4dd/41598_2017_3121_Fig1_HTML.jpg

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