Jing Li1, Xinming Li1, Xianyue Quan1, Genwen Hu2, Yingjie Mei3, Da Shi1, Shisi Li4, Zhendong Qi1, and Xiao Zhang5
1Zhujiang Hospital, Southern Medical University, Guangzhou, China, 2Shenzhen People’s Hospital, Clinical Medical College of Jinan University, Shenzhen, China, 3Phlips Healthcare, Guangzhou, China, 4The Third Affiliated Hospital of Southern Medical University, Guangzhou, China, 5Guangdong Provincial Key Laboratory of Medical Image Processing, School of Biomedical Engineering, Southern Medical University, Guangzhou, China
Synopsis
To
explore the potential of histogram analysis to evaluate the liver fibrosis
stages, histogram of T1rho and ADC were acquired from liver fibrosis model
built in seventy-five rats by injecting 50% carbon tetrachloride and olive oil.
In this study, we found that the parameters of histogram analysis showed strong
correlations with liver fibrosis stages, as well as inflammatory activity,while T1rho is regarded to be better than ADC.
Introduction
Early diagnosis and staging of liver fibrosis
are vital clinical components[1]. Both T1 relaxation
time in the rotating frame (T1rho) and apparent diffusion coefficient (ADC)
have been employed and play a valuable role in differentiating liver fibrosis
stages[2, 3]. However, routine MR
signal measurements in previous studies only provide mean values, which may
less effectively reflect spatial distribution underlying the MR signal.
Histogram analysis is a new method to obtain the heterogeneity within region of
interests (ROIs)[4, 5]. Therefore, we aim
to investigate the diagnosis value of both T1rho and ADC histogram analysis
in evaluating and quantifying liver fibrosis, as well as the potential influence
of inflammatory activity.Material and Method
Seventy-five
male Sprague-Dawley rats were randomly divided into four experimental group
(n=57) and one control group (n=18). Liver fibrosis model was established by
subcutaneous injection of 50% carbon tetrachloride (CCl4) and olive oil. T1rho and ADC (gradient factor b-values of 0 and 800 s/mm2) were performed with a
3.0T clinical scanner(Achieva 3.0T TX, Philips Healthcare, Best, Netherlands), using
an animal coil. T1rho was performed using turbo field echo (TFE) sequence,
scanning parameters were as follow: TR/TE=4.2ms/2.1ms; FOV=60mm*60mm; slice
thickness=2mm; number of slice=5; flip angle=10°, matrix=100*100; spinlock frequency=500Hz; spin
lock time=0, 27, 54ms respectively. The liver tissue was sampled for pathological test and liver
fibrosis staging. The histograms were derived from T1rho relaxation map and ADC
map. ROIs were drawn manually on axial imaging for 3D volume area, avoiding artifacts and large vessels. Entropy,
kurtosis, mean, median, skewness, uniformity and 10th and 90th percentiles
were generated and compared according to the liver fibrosis stage and
inflammatory activity.Results and Discussion
75 rats were included in total, and 18, 18, 17, 11, and 11 rats were
diagnosed as F0-F4. Entropy, kurtosis, mean, median, skewness, uniformity and
10th and 90th percentiles of both T1rho and ADC demonstrated significant correlation with
fibrosis stage(r=-0.603 to 0.757, p<0.001) and inflammatory activity (r=-0.620
to 0.763, p<0.001 to p=0.016) (Table1,2). To distinguish the fibrosis stage F≥1 and F≥4, 90th percentiles
of T1rho map acquired AUCs of 0.988 and 0.892, and at the same time 0.823 and
0.712 for median of ADC map. ROC curves showed that 90th percentiles
of T1rho map achieved remarkably higher AUCs than
median of ADC map, and statistical significance existed in pairwise comparisons
(p=0.0006 and p=0.013) (Fig 3).Conclusion
Histogram analysis of both T1rho and ADC exhibited
significant correlations with the stages of liver fibrosis and inflammatory
activity, while the former is considered superior to the latter one in staging
liver fibrosis.Acknowledgements
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