Dipolar order mapping based on spin-lock magnetic resonance imaging

preprint2026arXivOpen access

Abstract

Purpose: Inhomogeneous magnetization transfer (ihMT) effect reflects dipolar order with a dipolar relaxation time (T1DT_{1D}), specific to motion-restricted macromolecules. We aim to quantify T1DT_{1D} using spin-lock MRI technique. Methods: In the proposed method, we introduce a T1DT_{1D}-specific ratio, denoted as RATIOdoslRATIO_{dosl}. This ratio is derived from the distinct relaxation rate RdoslR_{dosl}, calculated as the difference between dual-frequency relaxation R1ρdualR_{1ρ}^{dual} and single-frequency R1ρsingleR_{1ρ}^{single} relaxation measurements. A novel rotary-echo spin-lock sequence was developed to enable dual-frequency spin-lock acquisition. We established a framework to estimate T1DT_{1D}, 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 RATIOdoslRATIO_{dosl} to T1DT_{1D}, and substantiated the accuracy and robustness of the proposed methods. Phantom experiments demonstrated robust ihMT contrast and confirmed the capability of T1DT_{1D} quantification via RATIOdoslRATIO_{dosl}. In vivo studies supported the clinical viability of this approcah, achieving simultaneous T1DT_{1D} and MPF mapping using only three spin-lock prepared images. Across ten healthy volunteers, the mean white matter T1DT_{1D} ranged from approximately 3.70 to 4.80 ms. Conclustion: We propose a novel method for T1DT_{1D} quantification based on spin-lock MRI. By requiring only three contrast-prepared images, this technique provides a promising pathway for robust, rapid, and simultaneous T1DT_{1D} and MPF quantification with fewer confounds

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