1. How does 2D-SWE with ATI compare to TE with CAP?
2D-SWE with ATI has theoretical advantages over TE with CAP, including easy incorporation into routine B-mode US examinations and accurate selection of the measurement region of interest (ROI) guided by simultaneously provided B-mode images. However, it is unclear whether these theoretical advantages translate into improved diagnostic performance in assessing liver fibrosis and hepatic steatosis compared to TE with CAP. Therefore, a study was conducted to compare CAP with ATI in the diagnosis of steatosis and to compare TE with 2D-SWE in the diagnosis of fibrosis in a NAFLD patient cohort. The results of this study will provide valuable insights into the potential benefits of using 2D-SWE with ATI over TE with CAP in the diagnosis of liver fibrosis and hepatic steatosis in NAFLD patients.
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2. What criteria were used for patient enrollment in the previous NAFLD cohort study?
In the previous NAFLD cohort study, patients with elevated liver enzymes or clinical suspicion of NASH were enrolled using specific criteria. These criteria included no history of positivity for hepatitis B virus surface antigen, antihepatitis C virus, hepatitis C virus RNA, and hepatitis B virus DNA. Additionally, patients with excessive alcohol consumption greater than the recommended limit (>14 UK units/wk for women and >21 UK units/wk for men) were excluded. Patients with liver pathology other than NAFLD on histopathologic examinations were also excluded. Potential living liver donors who underwent liver biopsy for NAFLD evaluation were enrolled if they met the inclusion criteria of having available results of TE with CAP and reliable LS measurement results obtained from TE.
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3. What is the measurement protocol for 2D-SWE and ATI?
The measurement protocol for 2D-SWE and ATI involves five abdominal radiologists from five institutions establishing a unified method. US examinations are performed using Aplio i800 scanners with a 1-8-MHz convex probe. Participants fast for at least 6 hours before the examination. The liver biopsy is performed in the right anterior section, avoiding reverberation artifacts. A sample box of 2D-SWE measuring 1.5x1.5 cm is placed on the liver parenchyma, and a 1-cm circular measurement ROI is used to obtain the LS value. The LS values are measured 10 times, and the median value is used for analysis. The 2D-SWE measurements are considered reliable if the IQR/median value is less than 30%. After 2D-SWE evaluation, ATI is performed in the right hepatic lobe through the intercostal window. A 2x4-cm square measurement ROI is placed in the sample box, avoiding areas of reverberation artifacts or large hepatic vessels. The attenuation coefficient (AC) in dB/cm/MHz is measured five times, and the median value is used. An R-value of 0.80 or higher indicates a reliable measurement.
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4. What technology does FibroScan use to measure liver stiffness and attenuation?
FibroScan uses vibration-controlled TE technology to simultaneously measure liver stiffness (LS) and attenuation (CAP). The CAP was designed to measure liver US attenuation at 3.5 MHz on both M and XL probes on signals acquired by FibroScan. CAP and LS measurements were expressed as dB/m and kPa, respectively. LS measurements were considered reliable if the IQR/median value was less than 30%, according to the liver elastography guidelines originally developed for TE [30, 31].
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