Quantitative macromolecular proton fraction imaging using pulsed spin‐lock

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Main Authors: Qianxue Shan, Ziqiang Yu, Baiyan Jiang, Jian Hou, Qiuyi Shen, Winnie Chiu Wing Chu, Vincent Wai Sun Wong, Weitian Chen
Format: Artículo Open Access
Published: Wiley 2025
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author Qianxue Shan
Ziqiang Yu
Baiyan Jiang
Jian Hou
Qiuyi Shen
Winnie Chiu Wing Chu
Vincent Wai Sun Wong
Weitian Chen
author_facet Qianxue Shan
Ziqiang Yu
Baiyan Jiang
Jian Hou
Qiuyi Shen
Winnie Chiu Wing Chu
Vincent Wai Sun Wong
Weitian Chen
Qianxue Shan
Ziqiang Yu
Baiyan Jiang
Jian Hou
Qiuyi Shen
Winnie Chiu Wing Chu
Vincent Wai Sun Wong
Weitian Chen
collection Wiley Open Access
contents Quantitative macromolecular proton fraction imaging using pulsed spin‐lock Qianxue Shan Ziqiang Yu Baiyan Jiang Jian Hou Qiuyi Shen Winnie Chiu Wing Chu Vincent Wai Sun Wong Weitian Chen Magnetic Resonance in Medicine AbstractPurposeRecent studies have shown that spin‐lock MRI can simplify quantitative magnetization transfer (MT) by eliminating its dependency on water pool parameters, removing the need for a T1 map in macromolecular proton fraction (MPF) quantification. However, its application is often limited by the requirement for long radiofrequency (RF) pulse durations, which are constrained by RF hardware capabilities despite remaining within specific absorption rate (SAR) safety limits.MethodsTo address this challenge, we propose a novel method, MPF mapping using pulsed spin‐lock (MPF‐PSL). MPF‐PSL employs a pulsed spin‐lock train with intermittent free precession periods, enabling extended total spin‐lock durations without exceeding hardware and specific absorption rate limits. A comprehensive analytical framework was developed to model the magnetization dynamics of the two‐pool MT system under pulsed spin‐lock, demonstrating that MPF‐PSL achieves MT‐specific quantification while minimizing confounding effects from the water pool. The proposed method is validated with Bloch–McConnell simulations, phantoms, and in vivo studies at 3T.ResultsBoth Bloch–McConnell simulations and phantom validation demonstrated that MPF‐PSL exhibits insensitivity to water pool parameters while enabling robust MPF quantification. In vivo validation studies confirmed the method's clinical utility in detecting collagen deposition in patients with liver fibrosis.ConclusionMPF‐PSL presents a practical solution for quantitative MT imaging, with strong potential for clinical applications. 10.1002/mrm.70021 http://creativecommons.org/licenses/by/4.0/
doi_str_mv 10.1002/mrm.70021
format Artículo Open Access
id wiley_oa_10_1002_mrm_70021
institution Wiley Open Access
license_str_mv http://creativecommons.org/licenses/by/4.0/
publishDate 2025
publisher Wiley
record_format wiley_oa
spellingShingle Quantitative macromolecular proton fraction imaging using pulsed spin‐lock
Qianxue Shan
Ziqiang Yu
Baiyan Jiang
Jian Hou
Qiuyi Shen
Winnie Chiu Wing Chu
Vincent Wai Sun Wong
Weitian Chen
Magnetic Resonance in Medicine
Quantitative macromolecular proton fraction imaging using pulsed spin‐lock Qianxue Shan Ziqiang Yu Baiyan Jiang Jian Hou Qiuyi Shen Winnie Chiu Wing Chu Vincent Wai Sun Wong Weitian Chen Magnetic Resonance in Medicine AbstractPurposeRecent studies have shown that spin‐lock MRI can simplify quantitative magnetization transfer (MT) by eliminating its dependency on water pool parameters, removing the need for a T1 map in macromolecular proton fraction (MPF) quantification. However, its application is often limited by the requirement for long radiofrequency (RF) pulse durations, which are constrained by RF hardware capabilities despite remaining within specific absorption rate (SAR) safety limits.MethodsTo address this challenge, we propose a novel method, MPF mapping using pulsed spin‐lock (MPF‐PSL). MPF‐PSL employs a pulsed spin‐lock train with intermittent free precession periods, enabling extended total spin‐lock durations without exceeding hardware and specific absorption rate limits. A comprehensive analytical framework was developed to model the magnetization dynamics of the two‐pool MT system under pulsed spin‐lock, demonstrating that MPF‐PSL achieves MT‐specific quantification while minimizing confounding effects from the water pool. The proposed method is validated with Bloch–McConnell simulations, phantoms, and in vivo studies at 3T.ResultsBoth Bloch–McConnell simulations and phantom validation demonstrated that MPF‐PSL exhibits insensitivity to water pool parameters while enabling robust MPF quantification. In vivo validation studies confirmed the method's clinical utility in detecting collagen deposition in patients with liver fibrosis.ConclusionMPF‐PSL presents a practical solution for quantitative MT imaging, with strong potential for clinical applications. 10.1002/mrm.70021 http://creativecommons.org/licenses/by/4.0/
title Quantitative macromolecular proton fraction imaging using pulsed spin‐lock
topic Magnetic Resonance in Medicine
url https://onlinelibrary.wiley.com/doi/10.1002/mrm.70021