The purpose of this study was to compare the ability of Gd-EOB-DTPA-enhanced signal intensity (SI) and T1 relaxation time-based indices for evaluation of liver function. We used Gd-EOB-DTPA-enhanced MRI and Look-Locker sequences to acquire conventional MRI and T1mapping images. The SI values of the liver, paravertebral muscle, T1 relaxation times of the liver before Gd-EOB-DTPA administration and in HBP were measured, the relative enhancement of the liver, increase rates of liver-to-muscle ratio, reduction rates of T1 relaxation time and ΔR1 were calculated, our study showed that the indices derived from T1 relaxation time were superior to SI-based indices.
101 patients with chronic viral hepatitis B and cirrhosis were separated into three groups in this prospective study: liver cirrhosis with Child-Pugh A (LCA, n=48), Child-Pugh B (LCB, n=40), Child-Pugh C (LCC, n=13). 21 healthy volunteers with normal liver function (NLF) were enrolled as control group. All subjects were underwent Gd-EOB-DTPA-enhanced MR imaging [native phase, arterial phase, portal venous phase, delayed phase and hepatobiliary phase (HBP)]. Look-Locker sequences with the same geometry position (the level of porta hepatis) were performed before Gd-EOB-DTPA administration and in HBP to acquire T1mapping. The SI values of the liver (SIpre/SIHBP), SI values of the paravertebral muscle (musclepre/muscleHBP) and T1 relaxation time of the liver (T1pre/T1HBP) before Gd-EOB-DTPA administration and in HBP were measured. The relative enhancement of the liver (RE), increase rates of liver-to-muscle ratio (rLMR), reduction rates of T1 relaxation time of the liver (rrT1) and ΔR1 were calculated. One-way ANOVA was performed to compare SI and T1 relaxation time-based indices among different liver function groups. ROC curve analysis was used to evaluate the diagnostic performance of SI and T1 relaxation time-based indices in discriminating NLF-CH-LCA from LCB-LCC.
The SI and T1 relaxation time-based indices were calculated according to the following formula:
RE=(SIHBP- SIpre)/ SIpre
rLMR=[( SIHBP/ muscleHBP)-( SIpre/ musclepre)]/ ( SIpre/ musclepre)
rrT1=[(T1pre-T1HBP)/ T1pre]*100%
ΔR1=(1/ T1HBP)-(1/ T1pre)
SI and T1 relaxation time-based indices of different groups were shown in table 1. Diagnostic performance for discriminating NLF-CH-LCA from LCB-LCC were shown in table 2.
SIpre showed significantly different (P<0.05) between NLF and LCB or NLF and LCC. RE showed significantly different (P<0.05) between LCC and NLF or LCA, between LCA and LCB. SIHBP and rLMR were significantly (P<0.05) higher in NLF and LCA compared to LCB or LCC. T1pre was significantly (P<0.05) higher in NLF compared to other groups, significantly different (P<0.05) was also found between LCA and LCC. T1HBP, rrT1 and ΔR1 showed significantly different (P<0.05) between any two groups except between NLF and LCA.
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