4.5 Article

Simultaneous T1, T2, and T1ρ relaxation mapping of the lower leg muscle with MR fingerprinting

期刊

MAGNETIC RESONANCE IN MEDICINE
卷 86, 期 1, 页码 372-381

出版社

WILEY
DOI: 10.1002/mrm.28704

关键词

diabetic neuropathy; lower leg muscle; magnetic resonance fingerprinting; multiparametric mapping; T-1

资金

  1. National Institutes of Health [R01 DK114428, R01 DK106292, R01 AR076328-01A1, R01 AR068966]
  2. Center of Advanced Imaging Innovation and Research (CAI2R)
  3. NIBIB Biomedical Technology Resource Center [NIH P41 EB017183]

向作者/读者索取更多资源

The proposed TB-SL MRF sequence is fast and insensitive to B-1(+) and B-0 imperfections. It can simultaneously map T-1, T-2, T-1 rho, and B-1(+) in a single scan and can potentially be used to study muscle composition.
Purpose: To develop a novel MR-fingerprinting (MRF) pulse sequence that is insensitive to B-1(+) and B-0 imperfections for simultaneous T-1, T-2, and T-1. relaxation mapping. Methods: We implemented a totally balanced spin-lock (TB-SL) module to encode T-1 rho relaxation into an existing MRF framework that encoded T-1 and T-2. The spin-lock module used two 180 degrees pulses with compensatory phases to reduce T-1 rho sensitivity to B-1 and B-0 inhomogeneities. We compared T-1 rho measured using TB-SL MRF in Bloch simulations, model agar phantoms, and in vivo experiments to those with a self-compensated spin-lock preparation module (SC-SL). The TB-SL MRF repeatability was evaluated in maps acquired in the lower leg skeletal muscle of 12 diabetic peripheral neuropathy patients, scanned two times each during visits separated by about 30 days. Results: The phantom relaxation times measured with TB-SL and SC-SL MRF were in good agreement with reference values in regions with low B-1 inhomogeneities. Compared with SC-SL, TB-SL MRF showed in experiments greater robustness against severe B-1 inhomogeneities and in Bloch simulations greater robustness against B-1 and B-0. We measured with TB-SL MRF an average T-1 = 950.1 +/- 28.7 ms, T-2 = 26.0 +/- 1.2 ms, and T-1 rho = 31.7 +/- 3.2 ms in skeletal muscle across patients. Bland-Altman analysis demonstrated low bias between TB-SL and SC-SL MRF and between TB-SL MRF maps acquired in two visits. The coefficient of variation was less than 3% for all measurements. Conclusion: The proposed TB-SL MRF sequence is fast and insensitive to B-1(+) and B-0 imperfections. It can simultaneously map T-1, T-2, T-1 rho, and B-1(+) in a single scan and can potentially be used to study muscle composition.

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