Clinically feasible B1 field correction for multi-organ sodium imaging at 3 T

被引:4
|
作者
Vaeggemose, Michael [1 ,2 ]
Schulte, Rolf F. [3 ]
Laustsen, Christoffer [2 ]
机构
[1] GE Healthcare, DK-2605 Brondby, Denmark
[2] Aarhus Univ, MR Res Ctr, Dept Clin Med, Aarhus, Denmark
[3] GE Healthcare, Munich, Germany
关键词
B-1 field correction; clinically feasible protocol; multi-organ; sodium imaging; MAGNETIC-RESONANCE; NA-23; MRI; COILS; QUANTIFICATION; EXERCISE; PROTOCOL; BRAIN; TIME;
D O I
10.1002/nbm.4835
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Sodium MRI allows the non-invasive quantification of intra-organ sodium concentration. RF inhomogeneity introduces uncertainty in this estimated concentration. B-1 field corrections can be used to overcome some of these limitations. However, the low signal-to-noise ratio in sodium MRI makes accurate B-1 mapping in reasonable scan times challenging. The study aims to evaluate Bloch-Siegert off-resonance (BLOSI) B-1 field correction for sodium MRI using a 3D Fermat looped, orthogonally encoded trajectories (FLORET) read-out trajectory. We propose a clinically feasible B-1 field map correction method for sodium imaging at 3 T, evaluating five healthy subjects' brain, heart blood, kidneys, and thigh muscle. We scanned the subjects twice for repeatability measures and used sodium phantoms to determine organ total sodium concentration. Conventional proton scans were compared with sodium images for organ structural integrity. The BLOSI approach based on the 3D FLORET read-out trajectory was used in B-1 field correction and 3D density-adapted radial acquisition for sodium imaging. Results indicate improvements in sodium imaging based on B-1 field correction in a clinically feasible protocol. Improvements are determined in all organs by enhanced anatomical representation, organ homogeneity, and an increase in the total sodium concentration after applying a B-1 field correction. The proposed BLOSI-based B-1 field correction using a 3D FLORET read-out trajectory is clinically feasible for sodium imaging, which is shown in the brain, heart, kidney, and thigh muscle. This supports using fast B-1 field mapping in the clinical setting.
引用
收藏
页数:11
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