Related Experiment Video
Updated: Jul 8, 2025

08:59
Use of a Multi-compartment Dynamic Single Enzyme Phantom for Studies of Hyperpolarized Magnetic Resonance Agents
Published on: April 15, 2016
6.9K
Validation of single reference variable flip angle (SR-VFA) dynamic T1 mapping with T2 * correction using a novel
Michael A Malmberg1,2, Henrik Odéen2, Lorne W Hofstetter3
1Department of Biomedical Engineering, University of Utah, Salt Lake City, Utah, USA.
Magnetic Resonance in Medicine
|December 20, 2023
Summary
Single reference variable flip angle (SR-VFA) T1 mapping, with T2 * correction, accurately measures T1 values within 10% of inversion recovery (IR) reference measurements. This method shows promise for dynamic T1 mapping in MRI applications.
Area of Science:
- Magnetic Resonance Imaging (MRI)
- Quantitative MRI
- Biomedical Engineering
Background:
- Accurate T1 mapping is crucial for various MRI applications, including tissue characterization and contrast agent quantification.
- Traditional T1 mapping techniques can be time-consuming or susceptible to artifacts.
- Dynamic T1 mapping offers the potential for improved temporal resolution in imaging.
Purpose of the Study:
- To validate single reference variable flip angle (SR-VFA) dynamic T1 mapping against inversion recovery (IR) T1 measurements.
- To assess the impact of T2 * correction on the accuracy of SR-VFA T1 mapping.
- To evaluate the performance of SR-VFA T1 mapping under varying rotational speeds and echo times (TEs).
Main Methods:
- A custom agar phantom with a spatial gradient of T1 relaxation rates was used.
- Inversion recovery (IR) T1, variable flip angle (VFA) T1, and B1+ measurements were acquired.
- Multi-echo stack-of-radial dynamic images were acquired during phantom rotation, and B1+-corrected SR-VFA and SR-VFA-T2 * T1 maps were computed and compared to IR T1 maps.
Main Results:
- Both VFA and SR-VFA-T2 * T1 maps achieved accuracy within 10% of IR T1 measurements at low rotational speeds (mean accuracy: 2.3% ± 2.6% and 2.8% ± 2.6%, respectively).
- Increasing rotational speed reduced accuracy due to temporal smoothing, particularly where T1 slope was non-constant.
- T2 * correction consistently improved the accuracy and precision of SR-VFA T1 maps, especially at later echo times.
Conclusions:
- SR-VFA-T2 * dynamic T1 mapping demonstrates accuracy within 10% of reference IR T1 measurements in an agar phantom.
- The method is sensitive to rotational speed and echo time, with T2 * correction enhancing performance.
- Further validation in mixed fat-water phantoms and in vivo is warranted.

