Robust T1ρ , T2 , and T2 * mapping via spin-locked MOLED with synthetic data-driven deep learning reconstruction

OBJECTIVE: To address the challenges of rapid and robust quantitative MRI, particularly for T1ρ mapping, by developing and evaluating a novel technique-spin-locked multiple overlapping echo detachment (SL-MOLED)-for efficient mapping of T1ρ, T2, and T2* relaxation times with reduced sensitivity to B0/B1 inhomogeneities and spin-lock-related banding artifacts.&#xD;Approach: SL-MOLED integrates spin-lock preparation into the MOLED acquisition framework, enabling simultaneous mapping of T1ρ, T2, T2*, proton density, and estimation of ΔB0 and B1 in approximately 11 seconds per slice. A synthetic data-driven deep learning reconstruction framework was trained on Bloch-simulated datasets with explicitly modeled banding artifacts, allowing effective mitigation of artifact-related errors. Validation comprised numerical experiments, phantom studies, healthy volunteer experiments, and a preliminary patient evaluation. Reconstruction accuracy was assessed using the structural similarity index measure (SSIM), mean absolute error (MAE), Pearson's correlation coefficient (r), and Bland-Altman analysis, whereas repeatability was evaluated using the coefficient of variation (CV).&#xD;Main results: Numerical experiments showed that networks trained with artifact modeling improved SSIM by 0.1-0.2 and reduced MAE by 2-5 ms for T1ρ, T2, and T2* compared with models trained without artifact modeling, across varying B0/B1 inhomogeneities and spin-lock frequencies. Phantom studies demonstrated good agreement between SL-MOLED reconstructed maps and reference methods for T1ρ, T2, and T2* (r > 0.997, Bland-Altman bias < 3.4%). In vivo experiments confirmed strong correlations with reference maps (r ≥ 0.976) and good repeatability (CV < 3.3%). In a patient with multiple sclerosis, SL-MOLED detected elevated T1ρ values in lesions relative to normal-appearing white matter, while T2 and T2* showed smaller changes, indicating that each parameter may reflect different underlying pathological features.&#xD;Significance: SL-MOLED provides accurate, repeatable, and artifact-robust quantitative mapping within a substantially reduced acquisition time (~11 s per slice), offering a promising framework for reliable multi-parametric MRI with potential for clinical translation.&#xD.

Authors

Institutions

Publication Details

Journal
Physics in Medicine and Biology
Published
2026-08-14
DOI
https://doi.org/10.1088/1361-6560/ae9a2a
Primary Topic
Advanced MRI Techniques and Applications
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Robust T1ρ , T2 , and T2 * mapping via spin-locked MOLED with synthetic data-driven deep learning reconstruction

Shuhui Cai, Congbo Cai, Jian Wu, Yuchen Zheng et al.
Physics in Medicine and Biology
Advanced MRI Techniques and Applications
article

Robust T1ρ , T2 , and T2 * mapping via spin-locked MOLED with synthetic data-driven deep learning reconstruction

Shuhui Cai, Congbo Cai, Jian Wu, Yuchen Zheng, Taishan Kang, Weikun Chen, Jianfa Chen, Qing Lin
article en

Abstract

OBJECTIVE: To address the challenges of rapid and robust quantitative MRI, particularly for T1ρ mapping, by developing and evaluating a novel technique-spin-locked multiple overlapping echo detachment (SL-MOLED)-for efficient mapping of T1ρ, T2, and T2* relaxation times with reduced sensitivity to B0/B1 inhomogeneities and spin-lock-related banding artifacts.&#xD;Approach: SL-MOLED integrates spin-lock preparation into the MOLED acquisition framework, enabling simultaneous mapping of T1ρ, T2, T2*, proton density, and estimation of ΔB0 and B1 in approximately 11 seconds per slice. A synthetic data-driven deep learning reconstruction framework was trained on Bloch-simulated datasets with explicitly modeled banding artifacts, allowing effective mitigation of artifact-related errors. Validation comprised numerical experiments, phantom studies, healthy volunteer experiments, and a preliminary patient evaluation. Reconstruction accuracy was assessed using the structural similarity index measure (SSIM), mean absolute error (MAE), Pearson's correlation coefficient (r), and Bland-Altman analysis, whereas repeatability was evaluated using the coefficient of variation (CV).&#xD;Main results: Numerical experiments showed that networks trained with artifact modeling improved SSIM by 0.1-0.2 and reduced MAE by 2-5 ms for T1ρ, T2, and T2* compared with models trained without artifact modeling, across varying B0/B1 inhomogeneities and spin-lock frequencies. Phantom studies demonstrated good agreement between SL-MOLED reconstructed maps and reference methods for T1ρ, T2, and T2* (r > 0.997, Bland-Altman bias < 3.4%). In vivo experiments confirmed strong correlations with reference maps (r ≥ 0.976) and good repeatability (CV < 3.3%). In a patient with multiple sclerosis, SL-MOLED detected elevated T1ρ values in lesions relative to normal-appearing white matter, while T2 and T2* showed smaller changes, indicating that each parameter may reflect different underlying pathological features.&#xD;Significance: SL-MOLED provides accurate, repeatable, and artifact-robust quantitative mapping within a substantially reduced acquisition time (~11 s per slice), offering a promising framework for reliable multi-parametric MRI with potential for clinical translation.&#xD.

Physics in Medicine and Biology
Xiamen University (CN), Massachusetts General Hospital (US), Zhongshan Hospital of Xiamen University (CN)
National Natural Science Foundation of China, National Key Research and Development Program of China
Openalex Percentile: Top 10%
Advanced MRI Techniques and Applications
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.