High contrast cartilaginous endplate imaging using a 3D adiabatic inversion-recovery-prepared fat-saturated ultrashort echo time (3D IR-FS-UTE) sequence.
High contrast cartilaginous endplate imaging using a 3D adiabatic inversion-recovery-prepared fat-saturated ultrashort echo time (3D IR-FS-UTE) sequence.
复制标题
DOI:
10.1002/nbm.4579
复制
发表时间:
2021-10
影响因子:
2.9
通讯作者:
Ma YJ
中科院分区:
文献类型:
--
作者:
Lombardi AF;Wei Z;Wong J;Carl M;Lee RR;Wallace M;Masuda K;Chang EY;Du J;Ma YJ
Ultrashort echo time (UTE) sequences can image tissues with transverse T2/T2* relaxations too short to be efficiently observed on routine clinical MRI sequences, such as the vertebral body cartilaginous endplate (CEP). Here, we describe a 3D adiabatic inversion recovery-prepared fat-saturated ultrashort echo time (3D IR-FS-UTE) sequence to highlight the CEP of vertebral bodies in comparison to the intervertebral disc (IVD) and bone marrow fat (BF) at 3T. The IR-FS-UTE sequence used a 3D UTE sequence combined with an adiabatic IR preparation pulse centered in the middle of the water and fat peaks, while a fat saturation module was used to suppress the signal from fat. A slab-selective half pulse was used for signal excitation, and a 3D center-out cones trajectory was used for more efficient data sampling. The 3D IR-FS-UTE sequence was applied to an ex vivo human spine sample, as well as the spines of six healthy volunteers and of three patients with back pain. Bright continue lines representing signal from CEP were found in healthy IVDs. The measured contrast-to-noise ratio (CNR) was 18.5±4.9 between the CEP and BF, and 20.3±4.15 between the CEP and IVD for the six volunteers. Abnormal IVDs showed CEP discontinuity or irregularity in the sample and patients’ studies. In conclusion, the proposed 3D IR-FS-UTE sequence is feasible for imaging of the vertebral body’s CEP in vivo with high contrast.
登录
查看更多内容
DOI:
10.1016/s0140-6736(18)32203-7
发表时间:
2018-11-10
期刊:
Lancet (London, England)
影响因子:
--
作者:
GBD 2017 Causes of Death Collaborators
通讯作者:
GBD 2017 Causes of Death Collaborators
影响因子:
3.3
作者:
Du J;Takahashi AM;Bae WC;Chung CB;Bydder GM
通讯作者:
Bydder GM
影响因子:
5.9
作者:
Kühn JP;Hernando D;Meffert PJ;Reeder S;Hosten N;Laqua R;Steveling A;Ender S;Schröder H;Pillich DT
通讯作者:
Pillich DT
影响因子:
19.7
作者:
Fields, Aaron J.;Han, Misung;Lotz, Jeffrey C.
通讯作者:
Lotz, Jeffrey C.
影响因子:
3.3
作者:
Gurney, PT;Hargreaves, BA;Nishimura, DG
通讯作者:
Nishimura, DG