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.
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 CLDpatients 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 CLDpatients.