Purpose
To develop a 3D sequence for T1ρ relaxation mapping using radial volumetric encoding (3D‐T1ρ‐RAVE) and to evaluate the multi relaxation components in the liver of healthy controls and chronic liver disease (CLD) patients.
Methods
Fat saturation and T1ρ preparation modules were followed by a train of gradient‐echo acquisitions and T1 restoration delay. The series of T1ρ‐weighted images were fitted using mono‐exponential, bi‐exponential, and stretched‐exponential models. The repeatability and reproducibility of the proposed technique were evaluated on National Institute of Standards and Technology phantom by calculating the coefficient of variation between test‐retest scans on the same scanner and between two different 3T scanners, respectively. Mann‐Whitney U‐test was performed to assess differences in T1ρ components among patients (n = 3) and a control group (n = 10).
Results
The phantom study showed an error of 8.9% and 11.5% in mono T2 relaxation time measurement relative to the reference on 2 different scanners. The coefficient of variation for test‐retest scans performed on the same scanner was 5.7% and 2.4% for scans performed on 2 scanners. The comparison between healthy controls and CLD patients showed a significant difference (P < .05) in mono relaxation time (P = .002), stretched‐exponential relaxation parameter (P = .04). The Akaike information criteria C criterion showed 2.53 ± 0.9% (2.3 ± 0.3% for CLD) of the voxels are bi‐exponential while in 65.3 ± 5.8% (81.2 ± 0.06% for CLD) of the liver voxels, the stretched‐exponential model was preferred.
Conclusion
The 3D‐T1ρ‐RAVE sequence allows volumetric, multicomponent T1ρ assessment of the liver during free breathing and can distinguish between healthy volunteers and CLD patients.