Fast T1 and T2 mapping methods: the zoomed U-FLARE sequence compared with EPI and snapshot-FLASH for abdominal imaging at 11.7 Tesla

  • Géraldine Pastor
  • María Jiménez-González
  • Sandra Plaza-García
  • Marta Beraza
  • Torsten Reese
Research Article

DOI: 10.1007/s10334-016-0604-x

Cite this article as:
Pastor, G., Jiménez-González, M., Plaza-García, S. et al. Magn Reson Mater Phy (2017) 30: 299. doi:10.1007/s10334-016-0604-x
  • 131 Downloads

Abstract

Objective

A newly adapted zoomed ultrafast low-angle RARE (U-FLARE) sequence is described for abdominal imaging applications at 11.7 Tesla and compared with the standard echo-plannar imaging (EPI) and snapshot fast low angle shot (FLASH) methods.

Materials and methods

Ultrafast EPI and snapshot-FLASH protocols were evaluated to determine relaxation times in phantoms and in the mouse kidney in vivo. Owing to their apparent shortcomings, imaging artefacts, signal-to-noise ratio (SNR), and variability in the determination of relaxation times, these methods are compared with the newly implemented zoomed U-FLARE sequence.

Results

Snapshot-FLASH has a lower SNR when compared with the zoomed U-FLARE sequence and EPI. The variability in the measurement of relaxation times is higher in the Look–Locker sequences than in inversion recovery experiments. Respectively, the average T1 and T2 values at 11.7 Tesla are as follows: kidney cortex, 1810 and 29 ms; kidney medulla, 2100 and 25 ms; subcutaneous tumour, 2365 and 28 ms.

Conclusion

This study demonstrates that the zoomed U-FLARE sequence yields single-shot single-slice images with good anatomical resolution and high SNR at 11.7 Tesla. Thus, it offers a viable alternative to standard protocols for mapping very fast parameters, such as T1 and T2, or dynamic processes in vivo at high field.

Keywords

Magnetic resonance imaging Abdomen Relaxation Mice High-field 

Supplementary material

10334_2016_604_MOESM1_ESM.doc (106 kb)
Supplementary material 1 (DOC 105 kb)

Funding information

Funder NameGrant NumberFunding Note
SaveMe project

    Copyright information

    © ESMRMB 2017

    Authors and Affiliations

    1. 1.Molecular Imaging UnitCIC biomaGUNEDonostia-San SebastiánSpain
    2. 2.Metabolism DivisionJohns Hopkins UniversityBaltimoreUSA

    Personalised recommendations