Mengting Hu1, Nan Wang1, Ailian Liu1, Qingwei Song1, Renwang Pu1, Lihua Chen1, Jiazheng Wang2, and Zhiwei Shen2
1The First Affiliated Hospital of Dalian Medical University, Dalian, China, 2Philips Healthcare, Dalian, China
Synopsis
The occurrence and development of liver cirrhosis is accompanied by changes
in portal vein blood flow and intrahepatic blood flow, which may eventually
lead to liver implantation [1]. Liver-lobe-based IVIM-derived parameters
can be associated with cirrhosis [2]. 4D flow-MRI could scope the portal vein
blood flow [3]. In this study, we explored the correlation between the
perfusion paraments and quantitative values of blood flow in patients with liver
cirrhosis using IVIM and 4D flow-MRI, investigating the potential connections
between portal vein flow changes and liver cirrhosis.
Introduction
DWI is the non-invasive technique to detect the diffusion movement of water
molecules in living tissues. IVIM can distinguish the diffusion signal of
Brownian motion of water molecules in tissues from the perfusion signal formed
by capillary microcirculation, and is helpful to better describe the complex
signal attenuation modes in biological tissues and organs [4]. 4D flow MRI with motion encoding and volumetric
and isotropic acquisition achieves quantification of blood flow directions,
velocities, wall shear force and pressures in the relatively large vessels,
such as portal vein [5]. The purpose of this study is to assess the possible
correlation the perfusion paraments and quantitative values of blood
flow using liver IVIM and portal vein 4D
flow-MRI for cirrhosis patients.Methods
This study has been approved by the institutional IRB. 11 patients were
recruited with informed consent acquired from each subject. All patients were
scanned using a 3.0 T MR scanner (Ingenia CX, Philips Healthcare, the
Netherlands) with a 16-channel abdominal array coil. The MR protocols include T1WI, T2WI, DWI, IVIM, 4D Flow and DYNAMIC
sequence. For 4D Flow imaging, a
2D phase-contrast scan was performed first (axial, TR/TE = 4.4/2.7 ms, FOV =
200×200 mm2, resolution = 1.5×1.5×8 mm3, PC direction =
RL, PC velocity = 200 cm/s, scan time = 13 s) to measure the flow velocity in
the portal vein, as a reference for velocity encodings (VENC). The 4D Flow
sequence with 8-fold compressed sensing acceleration was scanned with the
following parameters: axial, TR/TE = 5.0/3.2 ms, FOV = 300×350 mm2,
resolution = 2.5×2.5×2.5 mm3, PC direction = RL-AP-FH, VENC = 30
cm/s, scan time = 4min37s. The detailed
parameters for all the other sequences were listed in Table 1. After the MR
scan is completed, the 4D flow images were processed on CVI42 package (Canada
Circle Cardiovascular Imaging)by an experienced radiologist to obtain the 3D
angiogram. Four planes were manually placed vertical on the targeted vessel
segments to measure the flow direction,the flow rate (cm/s), the
axial-wall shear stress (WSS, Pa), and the pressure gradient (mmHg). Three planes were placed at the proximal, middle,
and distal
of the main portal vein and one at the splenic vein confluence as reference
(Figure1). The images of other sequences were analyzed on a post-processing ISP
workstation (Intelli Space Portal, Philips Healthcare) to measure IVIM parameters included: sADC, D, D* and F (Figure2).
Spearman test (SPSS 22.0) was used to analyze the correlation between IVIM
parameters and 4D flow-MRI parameters.Results
sADC and D values were negatively correlated with the proximal Flow rate
(r=0.626, P<0.05) and the middle Flow rate (r=0.709, P<0.05),
respectively. D* value was positively correlated with the middle Flow and proximal
Flow rate (r=0.900, P=0.037). There was no correlation among the other
parameters (P>0.05).Discussion and Conclusion
The changes in portal blood flow during the development of liver cirrhosis were
associated with the variation of the signals in intrahepatic blood flow. There
is a certain correlation among sADC and D values measured by IVIM and flow rate
in 4D flow sequences. The mechanism behind this correlation need the further
investigation and may shed light on the disease assessment and the development
of novel therapies. Acknowledgements
No acknowledgement found.References
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