Home Determination of an Optimized Weighting Factor of Liver Parenchyma for Six-point Interference Dixon Fat Percentage Imaging Accuracy in Nonalcoholic Fatty Liver Disease Rat Model
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Determination of an Optimized Weighting Factor of Liver Parenchyma for Six-point Interference Dixon Fat Percentage Imaging Accuracy in Nonalcoholic Fatty Liver Disease Rat Model

Rationale and Objectives

The aim of this study was to determine the optimal weighting factor (WF) for precise quantification using six-point interference Dixon fat percentage imaging by analyzing changes in WFs of fatty acid metabolites (FMs) in high-fat-induced fatty liver disease rat model.

Materials and Methods

Individual FM-related WFs were calculated based on concentration ratios of integrated areas of seven peak FMs with four phantom series. Ten 8-week-old male Sprague-Dawley rats were used for baseline quantification of fat in liver magnetic resonance imaging or magnetic resonance spectroscopy data. These seven lipid metabolites were then quantitatively analyzed. Spearman test was used for correlation analysis of different lipid proton concentrations. The most accurate WF for six-point interference Dixon fat percentage imaging was then determined.

Results

The seven lipid resonance WF values obtained from magnetic resonance spectroscopy data for three different oils (oleic, linoleic, and soybean) were different from each other. In lipid phantoms, except for the phantom containing oleic acid, changes in FP values were significantly different when WFs were changed in six-point interference Dixon fat percentage image. The seven lipid resonance WF values for the nonalcoholic fatty liver animal model were different from human subcutaneous adipose tissue lipid WF values.

Conclusions

WF affected the calculation of six-point interference Dixon-based fat percentage imaging value in phantom experiment. If WF of liver parenchyma FM which is specific to each liver disease is applied, the accuracy of six-point interference Dixon fat percentage imaging can be further increased.

Introduction

Hepatic steatosis is a common disease that affects nearly 30% of the world’s adult population . It can progress to liver fibrosis over time. It frequently causes liver cirrhosis or hepatic cellular carcinoma . Furthermore, transplantation of a moderately fatty liver can increase the risk of liver failure, making the evaluation of a donor’s liver fat deposition extremely important .

Although liver biopsy is considered the most reliable procedure for evaluating fatty liver, it cannot be repeatedly done as it is an invasive examination with limitations such as potential for sampling error and interobserver variations . As a result, noninvasive methods are increasingly used for the evaluation of fatty liver. Among those techniques, the use of ultrasound scan also has disadvantages because it is highly sonographer-dependent without providing quantitative results .

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Figure 1, Phantom series magnetic resonance spectroscopy (MRS) data profile obtained by LCModel analysis. The concentration of lipid proton varies according to the type of oil in the phantom experiment. (a), (b), (c) , and (d) are test tubes of oleic acid, linoleic acid, soybean oil 1, and soybean oil 2, respectively. Linoleic acid (b) does not have a diallylic proton expressed at 2.8 ppm. As shown in phantom data of (c) and (d) , the same lipid profile is observed in MRS data even at different lipid/water ratios. (Color version of figure is available online.)

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Materials and Methods

Phantom Experiment and Magnetic Resonance Imaging (MRI)/Proton Magnetic Resonance Spectroscopy ( 1 H MRS) Acquisition

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Figure 2, Phantom series comprised four test tubes. (a) Oleic acid, (b) linoleic acid, (c) soybean oil 1, and (d) soybean oil 2 with different oil-to-water ratios compared to test tube (c) . The red box is the region of interest (12 × 10 mm 2 ) for measuring the fat percentage (FP) value. (Color version of figure is available online.)

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WF Calculation From Phantom Series MRS Data

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Various WFs for Six-point Interference Dixon Fat Percentage Image Acquisition and Analysis

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High-Fat Diet Fatty Liver Rat Model MRS Experimental Protocol and Analysis

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Results

WF Calculation According to Phantom MRS Data and Six-point Interference Dixon Fat Percentage Imaging Experiment

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TABLE 1

The Weighting Factor (WF) Values of Each Lipid Proton as the Fatty Acid Phantom Magnetic Resonance Spectroscopy Data

0.9 ppm 1.3 ppm 1.6 ppm 2.03 ppm 2.25 ppm 2.77 ppm 5.3 ppm WF ref 0.082 0.627 0.071 0.095 0.065 0.015 0.041 WF 1 0.0847 0.773 0.000 0.069 0.036 0.000 0.034 WF 2 0.126 0.549 0.022 0.088 0.077 0.092 0.043 WF 3 0.094 0.653 0.025 0.053 0.067 0.059 0.045 WF 4 0.097 0.643 0.029 0.058 0.075 0.061 0.034

Figure 3, Difference in mean fat percentage (FP) value depending on four different weighting factors (WFs). (a), (b), (c) , and (d) are 6-pt-Dixon FP data of test tubes 1, 2, 3, and 4, respectively. The linoleic acid test tube (b) , in which diallylic protons were not observed in MRS phantom data ( Fig 1 ), showed the largest change in FP concentration when a different WF was applied.

TABLE 2

The Analysis of Variance Test of Lipid Phantom Series Depending on the Applied Four Different WFs (WF ref , WF 1 , WF 2 , WF ave3,4 )

Test Tube Sum of Squares_P_ Value Intra-Group Inter-Group Oleic acid 1.232 7.765 .146 Linoleic acid 9.652 1.721 .000 Soybean oil 1 13.902 6.188 .000 Soybean oil 2 2.934 5.981 .002

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WF Values Change of High-fat Diet Fatty Liver Rat Model

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TABLE 3

The Mean Value Change of Individual Lipid Proton Weighting Factors (WFs) as Rat Fatty Liver FP Group

0.9 ppm 1.3 ppm 1.6 ppm 2.03 ppm 2.25 ppm 2.77 ppm 5.3 ppm 0%–10% 0.069 0.691 0.048 0.034 0.063 0.038 0.053 11%–20% 0.062 0.691 0.043 0.038 0.065 0.046 0.052 21%–30% 0.056 0.671 0.064 0.037 0.069 0.048 0.050 >31% 0.067 0.700 0.042 0.034 0.064 0.042 0.048 Average WF 0.064 0.688 0.049 0.036 0.065 0.043 0.051P value .078 .240 .045 .321 .500 .207 .520

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Inter-FM Concentration Correlation Analysis

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TABLE 4

The Correlation Analysis Between Seven Lipid Proton Concentrations

0.9 ppm 1.3 ppm 1.6 ppm 2.03 ppm 2.25 ppm 2.77 ppm 5.3 ppm 0.9 ppm 1.000 0.426 ( P = .038) −0.599 ( P = .002) −0.273 ( P = .197) −0.525 ( P = .008) −0.362 ( P = .082) 0.117 ( P = .585) 1.3 ppm 0.426 (P = .038) 1.000 −0.871 ( P = .000) −0.626 ( P = .001) −0.730 ( P = .000) −0.826 ( P = .000) 0.353 ( P = .091) 1.6 ppm −0.599 ( P = .002) −0.871 ( P = .000) 1.000 0.430 ( P = .036) 0.561 ( P = .004) 0.612 ( P = .001) −0.305 ( P = .147) 2.03 ppm −0.273 ( P = .197) −0.626 ( P = .001) 0.430 ( P = .036) 1.000 0.580 ( P = .003) 0.803 ( P = .000) −0.712 ( P = .000) 2.25 ppm −0.525 ( P = .008) −0.730 ( P = .000) 0.561 ( P = .004) 0.580 ( P = .003) 1.000 0.842 ( P = .000) −0.411 ( P = .046) 2.77 ppm −0.362 ( P = .082) −0.826 ( P = .000) 0.612 ( P = .001) 0.803 ( P = .000) 0.842 ( P = .000) 1.000 −0.641 ( P = .001) 5.3 ppm 0.117 ( P = .585) 0.353 ( P = .091) −0.305 ( P = .147) −0.712 ( P = .000) −0.411 ( P = .046) −0.641 ( P = .001) 1.000

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Discussion

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Figure 4, Lipid proton acquisition and lipid proton profile after high-fat (HF) induction using the same animal model. (a) HF diet rat model four-channel animal coil mount and magnetic resonance spectroscopy (MRS) acquisition. T2-weighted three phase images (axial, sagittal, and coronal) were acquired to obtain liver MRS data. (b) and (c) are 2- and 8-week LCModel MRS data, respectively. No change in the ratio of lipid proton in MRS data obtained in different periods was observed. In other words, as weighting factor (WF) did not change according to difference in intrahepatic fat deposition, six-point interference Dixon fat percentage imaging could be applied by using the same WF even if the degree of fatty liver was different. (Color version of figure is available online.)

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Acknowledgments

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Supplementary Data

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Appendix S1

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