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在 9.4T 场强下,通过同时对多个光谱峰进行交替激发、采用灵活的扭曲投影成像读出轨迹,实现对人头部的 PCr/ATP 比映射成像。

PCr/ATP ratio mapping of the human head by simultaneously imaging of multiple spectral peaks with interleaved excitations and flexible twisted projection imaging readout trajectories at 9.4 T.

机构信息

Center for Magnetic Resonance Research, University of Illinois at Chicago, Chicago, Illinois 60612, USA.

出版信息

Magn Reson Med. 2013 Feb;69(2):538-44. doi: 10.1002/mrm.24281. Epub 2012 Apr 23.

DOI:10.1002/mrm.24281
PMID:22529019
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4552734/
Abstract

Quantitative (31)P magnetic resonance imaging of the whole human brain is often time-consuming even at low spatial resolution due to the low concentrations, long T(1) relaxation times, and low detection sensitivity of phosphorus metabolites. We report herein the results of combining the increased detection sensitivity of an ultra-high field 9.4 T scanner designed for human imaging with a new pulse sequence termed simultaneously imaging of multiple spectral peaks with interleaved excitations and flexible twisted projection imaging readout trajectories to rapidly sample multiple resonances in the (31)P spectrum. The phosphocreatine and γ-adenosine triphosphate images, obtained simultaneously from the entire human head, are demonstrated at 1.5 cm isotropic nominal resolution in a total acquisition time of 33 min. The phosphocreatine/γ-adenosine triphosphate ratio calculated for brain parenchyma (1-2) and the superficial temporalis muscle (3-5) are in agreement with literature values.

摘要

由于磷代谢物浓度低、T1 弛豫时间长且检测灵敏度低,对整个大脑进行定量 (31)P 磁共振成像是一项耗时的工作,即使在低空间分辨率下也是如此。我们在此报告了一种新方法的结果,该方法结合了专为人体成像设计的超高场 9.4 T 扫描仪的检测灵敏度的提高,以及一种新的脉冲序列,该序列称为同时激发多个光谱峰的成像和灵活的扭曲投影成像读出轨迹,以便在 (31)P 光谱中快速采集多个共振。在整个头部,在 33 分钟的总采集时间内,以 1.5 厘米各向同性名义分辨率获得磷肌酸和γ-三磷酸腺苷图像。计算得到的脑实质 (1-2) 和颞浅肌 (3-5) 的磷肌酸/γ-三磷酸腺苷比值与文献值一致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/957a/4552734/39a8920edfe2/nihms-365683-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/957a/4552734/5e9547905dc0/nihms-365683-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/957a/4552734/5a25bda0e44e/nihms-365683-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/957a/4552734/915f76b2fc1f/nihms-365683-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/957a/4552734/3b26f0e4a633/nihms-365683-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/957a/4552734/39a8920edfe2/nihms-365683-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/957a/4552734/5e9547905dc0/nihms-365683-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/957a/4552734/5a25bda0e44e/nihms-365683-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/957a/4552734/915f76b2fc1f/nihms-365683-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/957a/4552734/3b26f0e4a633/nihms-365683-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/957a/4552734/39a8920edfe2/nihms-365683-f0005.jpg

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