Prospective Study
Copyright ©The Author(s) 2025. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Mar 21, 2025; 31(11): 102795
Published online Mar 21, 2025. doi: 10.3748/wjg.v31.i11.102795
Attenuation imaging for hepatic steatosis in chronic hepatitis B vs metabolic dysfunction-associated steatotic liver disease
Xue-Qi Li, Guang-Wen Cheng, Iwaki Akiyama, Xian-Jue Huang, Jing Liang, Li-Yun Xue, Yi Cheng, Masatoshi Kudo, Hong Ding
Xue-Qi Li, Guang-Wen Cheng, Jing Liang, Li-Yun Xue, Yi Cheng, Hong Ding, Department of Ultrasound, National Clinical Research Center for Aging and Medicine, Huashan Hospital, Fudan University, Shanghai 200040, China
Iwaki Akiyama, Medical Ultrasound Research Center, Doshisha University, Kyoto 600-8586, Kyōto, Japan
Xian-Jue Huang, Department of General Surgery, Huashan Hospital, Fudan University, Shanghai 200040, China
Masatoshi Kudo, Department of Gastroenterology and Hepatology, Kindai University Faculty of Medicine, Osaka 577-8502, Japan
Co-first authors: Xue-Qi Li and Guang-Wen Cheng.
Co-corresponding authors: Masatoshi Kudo and Hong Ding.
Author contributions: Ding H and Kudo M contributed to study design; Li XQ and Cheng GW contributed to statistical analysis and interpretation of data; Li XQ, Cheng GW, Akiyama I, Huang XJ, Liang J, Xue LY, Cheng Y, Kudo M, Ding H contributed to data collection, manuscript draft and editing; All authors read and approved the final manuscript.
Supported by the National Natural Science Foundation of China, No. 82202185; and Shanghai Science and Technology Development Foundation, No. 22Y11911500.
Institutional review board statement: The prospective study was approved by the Medical Ethics Committee of Huashan Hospital of Fudan University (No. 2020-1204).
Clinical trial registration statement: This trial has been registered at Chinese Clinical Trial Registry, with the identifier No. ChiCTR2300069459.
Informed consent statement: All patients have signed informed consent.
Conflict-of-interest statement: The authors declare that they have no conflict of interest.
CONSORT 2010 statement: The authors have read the CONSORT 2010 Statement, and the manuscript was prepared and revised according to the CONSORT 2010 Statement.
Data sharing statement: No additional data are available.
Open Access: This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: https://creativecommons.org/Licenses/by-nc/4.0/
Corresponding author: Hong Ding, MD, PhD, Professor, Department of Ultrasound, National Clinical Research Center for Aging and Medicine, Huashan Hospital, Fudan University, No. 12 Urumqi Middle Road, Shanghai 200040, China. ding_hong@fudan.edu.cn
Received: November 5, 2024
Revised: January 25, 2025
Accepted: February 20, 2025
Published online: March 21, 2025
Processing time: 128 Days and 20.4 Hours
Abstract
BACKGROUND

Hepatic steatosis, characterized by fat accumulation in hepatocytes, can result from metabolic dysfunction-associated steatotic liver disease (MASLD), infections, alcoholism, chemotherapy, and toxins. MASLD is diagnosed via imaging or biopsy with metabolic criteria and may progress to metabolic dysfunction–associated steatohepatitis, potentially leading to fibrosis, cirrhosis, or cancer. The coexistence of hepatic steatosis with chronic hepatitis B (CHB) is mainly related to metabolic factors and increases mortality and cancer risks. As a noninvasive method, attenuation imaging (ATI) shows promise in quantifying liver fat, demonstrating strong correlation with liver biopsy.

AIM

To investigate the disparity of ATI for assessing biopsy-based hepatic steatosis in CHB patients and MASLD patients.

METHODS

The study enrolled 249 patients who underwent both ATI and liver biopsy, including 78 with CHB and 171 with MASLD. Hepatic steatosis was classified into grades S0 to S3 according to the proportion of fat cells present. Liver fibrosis was staged from 0 to 4 according to the meta-analysis of histological data in viral hepatitis scoring system. The diagnostic performance of attenuation coefficient (AC) values across different groups was compared for each grade of steatosis. Factors associated with the AC values were determined through linear regression analysis. A multivariate logistic regression model was established to predict ≥ S2 within the MASLD group.

RESULTS

In both the CHB and the MASLD groups, AC values increased significantly with higher steatosis grade (P < 0.001). In the CHB group, the areas under the curve (AUCs) of AC for predicting steatosis grades ≥ S1, ≥ S2 and S3 were 0.918, 0.960 and 0.987, respectively. In contrast, the MASLD group showed AUCs of 0.836, 0.774, and 0.688 for the same steatosis grades. The diagnostic performance of AC for detecting ≥ S2 and S3 indicated significant differences between the two groups (both P < 0.001). Multivariate linear regression analysis identified body mass index, triglycerides, and steatosis grade as significant factors for AC. When the steatosis grade is ≥ S2, it can progress to more serious liver conditions. A clinical model integrating blood biochemical parameters and AC was developed in the MASLD group to enhance the prediction of ≥ S2, achieving an AUC of 0.848.

CONCLUSION

The AC could effectively discriminate the degree of steatosis in both the CHB and MASLD groups. In the MASLD group, when combined with blood biochemical parameters, AC exhibited better predictive ability for moderate to severe steatosis.

Keywords: Metabolic dysfunction-associated steatotic liver disease; Chronic hepatitis B; Liver steatosis; Attenuation imaging; Attenuation coefficient

Core Tip: Our study demonstrated that for the same steatosis grade, the attenuation coefficient (AC) value was significantly higher in the metabolic dysfunction-associated steatotic liver disease (MASLD) group than that in the chronic hepatitis B group. AC effectively discriminated between the degree of steatosis in steatotic liver disease of various etiologies. In the MASLD group, to improve the ability to predict ≥ S2, a clinical model incorporating blood biochemical parameters and AC was established, with an area under the curve of 0.848. The predictive model demonstrated a sensitivity of 91.2% and a specificity of 71.8%.