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Relaxation-compensated fast multislice amide proton transfer (APT) imaging of acute ischemic stroke

✍ Scribed by Phillip Zhe Sun; Yoshihiro Murata; Jie Lu; Xiaoying Wang; Eng H. Lo; A. Gregory Sorensen


Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
705 KB
Volume
59
Category
Article
ISSN
0740-3194

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✦ Synopsis


Abstract

Amide proton transfer (APT) imaging is a variant form of chemical exchange saturation transfer (CEST) imaging that is based on the magnetization exchange between bulk water and labile endogenous amide protons. Given that chemical exchange is pH‐dependent, APT imaging has been shown capable of imaging ischemic tissue acidosis, and as such, may serve as a surrogate metabolic imaging marker complementary to perfusion and diffusion MRI. In order for APT imaging to properly diagnose heterogeneous pathologies such as stroke and cancer, fast volumetric APT imaging has to be developed. In this study the evolution of CEST contrast after RF irradiation was solved showing that although the CEST steady state is reached by the apparent longitudinal relaxation rate, the decreases of CEST contrast after irradiation is governed by the intrinsic relaxation constant. A volumetric APT imaging sequence is proposed that acquires multislice images immediately after a single long continuous wave (CW) RF irradiation, wherein the relaxation‐induced loss of CEST contrast is compensated for during postprocessing. The proposed technique was verified by numerical simulation, a tissue‐like dual‐pH phantom, and demonstrated on an embolic stroke animal model. In summary, our study has established a fast volumetric pH‐weighted APT imaging technique, allowing further investigation to fully evaluate its diagnostic power. Magn Reson Med 59:1175–1182, 2008. © 2008 Wiley‐Liss, Inc.


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✍ Phillip Zhe Sun; Jinyuan Zhou; Judy Huang; Peter van Zijl 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 334 KB

## Abstract Amide proton transfer (APT) imaging employs the chemical exchange saturation transfer (CEST) mechanism to detect mobile endogenous proteins and peptides. It can be used to detect pH reduction during acute ischemia and thus provide complementary information to perfusion‐weighted (PWI) an