Jing Zhang1, Yikai Xu1, Yihao Guo2, Yanqiu Feng2, Queenie Chen3, Yingjie Mei2,4, Xiangliang Tan1, Jiajun Zhang1, Xixi Zhao1, Zeyu Zheng1, and Chunhong Wang1
1Department of Medical Imaging Center, Nanfang Hospital, Southern Medical University, Guangzhou, China, People's Republic of, 2School of Biomedical Engineering and Guangdong Provincial Key Laboratory of Medical Image Processing, Southern Medical University, Guangzhou, China, People's Republic of, 3Philips Healthcare, Hong Kong, China, People's Republic of, 4Philips Healthcare, Guangzhou, China, People's Republic of
Synopsis
The quantitative evaluation of hepatic function is important for monitoring
patients and preoperative assessment of the hepatic reserve. This work aims to
assess the sensitivity of IVIM in evaluating liver function in patients with
chronic liver disease. The results demonstrate that perfusion-related
parameters (D* and f) are useful for indicating the severity of liver disease,
and may have the potential to become a promising non-invasive tool for
monitoring liver function.Introduction
The quantitative evaluation of hepatic function is important for monitoring
patients and preoperative assessment of the hepatic reserve1. In clinical practice, tests that assess global
liver function may fail to detect regional liver dysfunction. Thus, liver
function may be estimated more accurately by using imaging-based tests, which
can detect both regional and global liver function.
Intravoxel
incoherent motion (IVIM) diffusion-weighted imaging (DWI) is a promising method
for the assessment of diffuse liver disease, given its potential for providing
multi-parametric information and combinations of diffusion and perfusion
effects. Chronic liver diseases are associated with extracellular matrix
accumulation, which may affect both true diffusion and microcirculation. Therefor
this work aims to assess the sensitivity of IVIM in evaluating liver function
in patients with chronic liver disease.
Methods
Eighty
patients (57 men, 23 women; mean age, 54 ± 12 years) who had chronic liver disease and had undergone IVIM DWI using 10 different b values (0, 10, 30, 60, 100, 150, 200, 400, 600 and 1000 s/mm2) at 3.0 T MR scanner (Achieva, Philips Healthcare, The Netherlands) were included. IVIM DWI was performed by
using a respiratory
triggered single-shot echo planar imaging (EPI factor, 53) sequence with a
parallel imaging SENSE(SENSE factor, 2))( TR/TE, 1642/62 ms; matrix, 256; FOV, 375 × 302 × 176 mm; slice
thickness, 5 mm; slice gap, 0.5 mm; slices, 32; NSA, 2). Patients were subdivided into the following three groups 2:
patients with MELD scores ≤ 10 (n = 32), 11–18 (n = 23) and > 18 (n = 25). All curve-fitting algorithms were created using a
home-developed program based on MATLAB (MathWorks, Natick, MA) (Figure 1, 2). Pure molecular diffusion (D), pseudo-diffusion (D*),
perfusion fraction (f) and apparent
diffusion coefficient (ADC) values were calculated, and used to evaluate liver
function, as indicated by the MELD score. Intraclass correlation coefficients
(ICCs) were calculated to determine the consistency between the data gathered
by the two radiologists. One-way analysis of variance was used to evaluate IVIM
parameters in patients with different grades of liver function. Receiver
operating characteristic (ROC) curve analysis was used to determine diagnostic
accuracy
Results
The
ICC values of D, D*, f and ADC
between the two radiologists were 0.997, 0.986, 0.985 and 0.995, respectively. D*, f and
ADC values significantly decreased with increasing MELD scores (p < 0.001)(Table1,
2, Figure 3). MELD scores were inversely correlated with D*, f and ADC values (r = -0.672, r =
-0.605, r = -0.538, respectively). The areas under the curve (AUCs) of D* and f for evaluating liver function were
0.73–093 and 0.82–0.95, respectively (Table 3).
Discussion
Our
results showed generally good agreement of each parameter between the two
radiologists, even for the D* and f parameters,
suggesting that the use of whole-liver data extraction may increase the
stability of the data. In our study, true molecular diffusion coefficients (D values) were weakly correlated with MELD scores.
This suggests
that the association of reduced ADC values with advanced liver disease merely
reflects decreased perfusion in the microvessels rather than restricted
molecular diffusion in the tissue. In
chronic liver disease, liver fibrosis and elevated intrahepatic resistance lead
to a reduction in portal blood flow, the increase in hepatic arterial blood
flow is insufficient to fully offset the decrease in portal blood flow, which
leads to a reduction in D* values. Moreover, hepatic steatosis is often
observed in the impaired liver parenchyma, and has been associated with
decreased hepatic parenchymal perfusion. Both D* and f values are perfusion-related parameters, however, they pertain to
different characteristics of perfusion. D* values reflect endovascular blood
flow velocity, while f values reflect
vascular volume3. Our results demonstrated that f values significantly differed between different stages of liver
function, and the correlation of f
values with MELD scores was stronger than that of D* and ADC values with MELD
scores. Thus, f values may be a sensitive indicator for liver function
classification and warrant further research.
Conclusion
This study
demonstrates that perfusion-related parameters (D* and f) are useful for indicating the severity of liver disease, and may
have the potential to become a promising non-invasive tool for monitoring liver
function.
Acknowledgements
No acknowledgement found.References
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