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Correlation between Hepatic Fat Content Using 3-Echo 3-D Dixon Method and Intravoxel Incoherent Motion (IVIM) Perfusion MR Imaging
Authors:Seung-Man Yu  Sae-Sark Kim  Mun-Young Paek  Eun-Hoe Goo  Youn-Sang Ji  Bo-Young Choe
Affiliation:1. Department of Biomedical Engineering, Research Institute of Biomedical Engineering, College of Medicine, The Catholic University of Korea, #505 Banpo-Dong, Seocho-Gu, Seoul, 137-040, Korea
2. Department of Radiology, Seoul National University Hospital, Seoul, 110-744, Korea
3. Department of Radiological Science, Gimcheon University, Gimcheon, 740-704, Korea
4. Siemens Healthcare, Seoul, Korea
5. Department of Radiological Technology, Cheongju University, Cheongju, 360-764, Korea
6. Department of Radiological Technology, Gwangju Health College University, Gwangju, 501-701, Korea
Abstract:Fat accumulates as droplets in the hepatocyte swelling, distortion of microcirculatory anatomy and compression of sinus. This study aims to investigate the correlation between the T2*-corrected fat fraction (FF) value acquired via gradient echo with a low flip angle and parenchymal pseudorandom blood perfusion (P fraction), microcirculation (D fast), and slow component of diffusion (D slow), acquired via intravoxel incoherent motion (IVIM), and to investigate the blood microcirculation and diffusion components of liver parenchyma, according to fat deposition. A total of 126 patients underwent 3-T magnetic resonance imaging, including a 3-echo three-dimensional (3-D) gradient echo sequence with T2*-corrected Dixon reconstruction and IVIM sequence. Pearson’s correlation analysis was conducted to investigate the correlation of the FF obtained via the Dixon method with the apparent diffusion coefficient (ADC), D slow, P fraction, and D fast obtained via IVIM. Correlation analysis was also conducted for the IVIM mapping images. A confidence level of p < 0.05 was set. A negative correlation was found between the T2*-corrected FF acquired using the 3-echo 3-D Dixon method and D slow acquired via IVIM (r = ?0.181, p < 0.05). It was likely due to the increased extracellular collagen deposition and increased intracellular fat droplets during the progression of liver fibrosis.
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