Abstract

PurposeUltrashort echo time (UTE) sequences play a key role in imaging and quantifying short T2 species. However, almost all of the relevant studies was conducted at relatively high fields. The purpose of this work was to further explore the feasibility of UTE imaging and T2* measurement for short T2 species at low fields.MethodsA 2D UTE sequence with an echo time (TE) of 0.37 ms was developed on a 0.35 T permanent magnet scanner. This sequence acquires multiecho images to fit the monoexponential signal decay model for quantitative T2* calculations. In the phantom experiments, MnCl2 solutions with different T2* values were used to assess the curve fitting model in low fields. In the in vivo experiments, T2* measurements were performed on the Achilles tendon of five normal volunteers.ResultsThe phantom studies showed a significant linear relationship between the MnCl2 solution concentration and R2* (1/T2*) values, which indicated the stability and accuracy of the T2* quantification model. The in vivo studies demonstrated that mean T2* value of Achilles tendon is 1.83 ± 0.21 ms, and the mean coefficient of determination (R-squared) was 0.996.ConclusionsBoth phantom and in vivo experiments showed that UTE imaging and quantification for short T2 components were feasible at low field 0.35 T scanner. This pilot study presents preliminary conclusions for future work.

Highlights

  • Biological tissues frequently contain different water components, which results in different distinct transverse relaxation times (T2) or apparent transverse relaxation times (T2*) during MR examination [1]

  • Ultrashort echo time (UTE) technique using radial ramp sampling and half pulse excitation can achieve a minimal TE before the transverse relaxation signal has significantly

  • The RF shape was redesigned by the variable-rate selective excitation (VERSE) technique to fit the down-ramp of the slice-select gradient

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Summary

Introduction

Biological tissues frequently contain different water components, which results in different distinct transverse relaxation times (T2) or apparent transverse relaxation times (T2*) during MR examination [1]. Quantitative relaxation time calculations are usually based on exponential fitting of data obtained from multiecho gradient echo sequences or Carr–Purcell–Meiboom–Gill sequences [2, 3]. There are a variety of short T2 tissues in the musculoskeletal system, and the average T2* values for these tissues range from several milliseconds down to tens of microseconds [4, 5]. Conventional magnetic resonance imaging employs T1 and T2 weighted sequences has a relatively longer echo time (TE). Even with gradient echo (GRE) sequences with TEs down to about 2 ms, short T2 tissues have little signal that can be detected [6]. Ultrashort echo time (UTE) technique using radial ramp sampling and half pulse excitation can achieve a minimal TE before the transverse relaxation signal has significantly

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