Three-dimensional ultrashort echo time cones T1ρ (3D UTE-cones-T1ρ) imaging
Three-dimensional ultrashort echo time cones T1ρ (3D UTE-cones-T1ρ) imaging
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DOI:
10.1002/nbm.3709
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发表时间:
2017-06-01
影响因子:
2.9
通讯作者:
Du, Jiang
中科院分区:
文献类型:
--
作者:
Ma, Ya-Jun;Carl, Michael;Du, Jiang
We report a novel three-dimensional (3D) ultrashort echo time (UTE) sequence employing Cones trajectory and T-1 preparation (UTE-Cones-T-1) for quantitative T-1 assessment of short T-2 tissues in the musculoskeletal system. A basic 3D UTE-Cones sequence was combined with a spin-locking preparation pulse for T-1 contrast. A relatively short TR was used to decrease the scan time, which required T-1 measurement and compensation using 3D UTE-Cones data acquisitions with variable TRs. Another strategy to reduce the total scan time was to acquire multiple Cones spokes (N-sp) after each T-1 preparation and fat saturation. Four spin-locking times (TSL=0-20ms) were acquired over 12min, plus another 7min for T-1 measurement. The 3D UTE-Cones-T-1 sequence was compared with a two-dimensional (2D) spiral-T-1 sequence for the imaging of a spherical CuSO4 phantom and ex vivo meniscus and tendon specimens, as well as the knee and ankle joints of healthy volunteers, using a clinical 3-T scanner. The CuSO4 phantom showed a T-1 value of 76.5 +/- 1.6ms with the 2D spiral-T-1 sequence, as well as 85.7 +/- 3.6 and 89.2 +/- 1.4ms for the 3D UTE-Cones-T-1 sequences with N-sp of 1 and 5, respectively. The 3D UTE-Cones-T-1 sequence provided shorter T-1 values for the bovine meniscus sample relative to the 2D spiral-T-1 sequence (10-12ms versus 16ms, respectively). The cadaveric human Achilles tendon sample could only be imaged with the 3D UTE-Cones-T-1 sequence (T-1=4.0 +/- 0.9ms), with the 2D spiral-T-1 sequence demonstrating near-zero signal intensity. Human studies yielded T-1 values of 36.1 +/- 2.9, 18.3 +/- 3.9 and 3.1 +/- 0.4ms for articular cartilage, meniscus and the Achilles tendon, respectively. The 3D UTE-Cones-T-1 sequence allows volumetric T-1 measurement of short T-2 tissues in vivo.