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Clinic-pathological features of metabolic associated fatty liver disease with hepatitis B virus infection

Authors :
Yueyong Zhu
Bo Wan
You-Bing Li
Yinlian Wu
Mingfang Wang
Jiaofeng Huang
Source :
World Journal of Gastroenterology
Publication Year :
2021
Publisher :
Baishideng Publishing Group Inc., 2021.

Abstract

BACKGROUND Metabolic associated fatty liver disease (MAFLD) is a novel concept proposed in 2020. AIM To compare the characteristics of MAFLD and MAFLD with hepatitis B virus (HBV) infection. METHODS Patients with histopathologically proven MAFLD from a single medical center were included. Patients were divided into MAFLD group (without HBV infection) and HBV-MAFLD group (with HBV infection). Propensity score matching was utilized to balance the baseline characteristics between two groups. RESULTS A total of 417 cases with MAFLD were included, 359 (86.1%) of whom were infected with HBV. There were significantly more males in the HBV-MAFLD group than in the MAFLD group (P < 0.05). After propensity score matching, 58 pairs were successfully matched with no significant differences found in gender, age, body mass index, lipid levels, liver enzymes, and the other metabolic associated comorbidities between the two groups (P > 0.05). The rank sum test results showed that the degree of liver steatosis in the MAFLD group was more severe than that in the HBV-MAFLD group, while the degree of inflammation and fibrosis in the liver was less severe (P < 0.05). In multivariate analysis, HBV infection was associated with significantly lower grade of hepatic steatosis [odds ratio (OR) = 0.088, 95% confidence interval (CI): 0.027-0.291] but higher inflammation level (OR = 4.059, 95%CI: 1.403-11.742) and fibrosis level (OR = 3.016, 95%CI: 1.087-8.370) after adjusting for age, gender, and other metabolic parameters. CONCLUSION HBV infection is associated with similar metabolic risks, lower steatosis grade, higher inflammation, and fibrosis grade in MAFLD patients.

Details

ISSN :
10079327
Volume :
27
Database :
OpenAIRE
Journal :
World Journal of Gastroenterology
Accession number :
edsair.doi.dedup.....a6326a60ddeb5d4567caf265fd1d7449