Measurement of APT using a combined CERT-AREX approach with varying duty cycles.
AUTHORS
- PMID: 28526431 [PubMed].
- PMCID: PMC5581699.
- NIHMSID: NIHMS878495
ABSTRACT
The goal is to develop an imaging method where contrast reflects amide-water magnetization exchange, with minimal signal contributions from other sources. Conventional chemical exchange saturation transfer (CEST) imaging of amides (often called amide proton transfer, or APT, and quantified by the metric MTR) is confounded by several factors unrelated to amides, such as aliphatic protons, water relaxation, and macromolecular magnetization transfer. In this work, we examined the effects of combining our previous chemical exchange rotation (CERT) approach with the non-linear AREX method while using different duty cycles (DC) for the label and reference scans. The dependencies of this approach, named AREX, on tissue parameters, including T, T, semi-solid component concentration (f), relayed nuclear Overhauser enhancement (rNOE), and nearby amines, were studied through numerical simulations and control sample experiments at 9.4T and 1μT irradiation. Simulations and experiments show that AREXis sensitive to amide-water exchange effects, but is relatively insensitive to T, T, f, nearby amine, and distant aliphatic protons, while the conventional metric MTRas well as several other APT imaging methods, are significantly affected by at least some of these confounding factors.
The goal is to develop an imaging method where contrast reflects amide-water magnetization exchange, with minimal signal contributions from other sources. Conventional chemical exchange saturation transfer (CEST) imaging of amides (often called amide proton transfer, or APT, and quantified by the metric MTR) is confounded by several factors unrelated to amides, such as aliphatic protons, water relaxation, and macromolecular magnetization transfer. In this work, we examined the effects of combining our previous chemical exchange rotation (CERT) approach with the non-linear AREX method while using different duty cycles (DC) for the label and reference scans. The dependencies of this approach, named AREX, on tissue parameters, including T, T, semi-solid component concentration (f), relayed nuclear Overhauser enhancement (rNOE), and nearby amines, were studied through numerical simulations and control sample experiments at 9.4T and 1μT irradiation. Simulations and experiments show that AREXis sensitive to amide-water exchange effects, but is relatively insensitive to T, T, f, nearby amine, and distant aliphatic protons, while the conventional metric MTRas well as several other APT imaging methods, are significantly affected by at least some of these confounding factors.
Tags: 2017