Dipolar order mapping based on spin-lock magnetic resonance imaging

Abstract

Purpose: Inhomogeneous magnetization transfer (ihMT) effect reflects dipolar order with a dipolar relaxation time (T1D), specific to motion-restricted macromolecules. We aim to quantify T1D using spin-lock MRI technique. Methods: In the proposed method, we introduce a T1D-specific ratio, denoted as RATIOdosl. This ratio is derived from the distinct relaxation rate Rdosl, calculated as the difference between dual-frequency relaxation R1ρdual and single-frequency R1ρsingle relaxation measurements. A novel rotary-echo spin-lock sequence was developed to enable dual-frequency spin-lock acquisition. We established a framework to estimate T1D, as well as the macromolecular pool fraction (MPF) map. The proposed approach was validated via numerical simulations, phantom studies, and demonstrated in vivo in human white matter. Results: Simulations revealed the high sensitivity of RATIOdosl to T1D, and substantiated the accuracy and robustness of the proposed methods. Phantom experiments demonstrated robust ihMT contrast and confirmed the capability of T1D quantification via RATIOdosl. In vivo studies supported the clinical viability of this approcah, achieving simultaneous T1D and MPF mapping using only three spin-lock prepared images. Across ten healthy volunteers, the mean white matter T1D ranged from approximately 3.70 to 4.80 ms. Conclustion: We propose a novel method for T1D quantification based on spin-lock MRI. By requiring only three contrast-prepared images, this technique provides a promising pathway for robust, rapid, and simultaneous T1D and MPF quantification with fewer confounds

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