Impact of prior HBV, HAV, and HEV infection on non‐alcoholic fatty liver disease

医学 内科学 脂肪肝 优势比 脂肪性肝炎 胃肠病学 血清学 乙型肝炎病毒 全国健康与营养检查调查 疾病 免疫学 病毒 人口 环境卫生 抗体
作者
Stephanos P. Vassilopoulos,Markos Kalligeros,Athanasios Vassilopoulos,Fadi Shehadeh,Gregorio Benitez,Matthew Kaczynski,Ingrid Lazaridou,Kittichai Promrat,Jack R. Wands,Eleftherios Mylonakis
出处
期刊:Journal of Viral Hepatitis [Wiley]
卷期号:30 (8): 685-693 被引量:3
标识
DOI:10.1111/jvh.13862
摘要

Non-alcoholic fatty liver disease (NAFLD) is a leading cause of chronic liver disease. The association between prior hepatitis B virus (HBV), hepatitis A virus (HAV), hepatitis E virus (HEV) infection and NAFLD remains unclear. We utilized the 2017-2020 National Health and Nutrition Examination Survey (NHANES) and performed multivariable logistic regression analyses to examine the association of prior HBV, HAV and HEV infection with NAFLD, as well as high risk non-alcoholic steatohepatitis (NASH) and liver fibrosis. Our analysis included 2565 participants with available anti-HBc serology results, 1480 unvaccinated participants with anti-HAV results, and 2561 participants with anti-HEV results. Among participants with NAFLD, the age-adjusted prevalence of prior HBV, HAV and HEV infection was 3.48%, 32.08% and 7.45%, respectively. Prior infection with HBV, HAV and HEV was not associated with NAFLD (cut-off 285 dB/m) [aOR: 0.99 (95% CI, 0.77-1.29), 1.29 (95% CI, 0.95-1.75), and 0.94 (95% CI, 0.70-1.27), respectively] or high-risk NASH [aOR 0.72 (95% CI, 0.45-1.17), 0.92 (95% CI, 0.55-1.52), and 0.89 (95% CI, 0.41-1.94), respectively]. Participants with anti-HBc and anti-HAV seropositivity were more likely to have significant fibrosis [aOR: 1.53 (95% CI, 1.05-2.23) and 1.69 (95% CI, 1.16-2.47), respectively]. The odds of significant fibrosis are 53%, and 69% greater for participants with prior history of HBV and HAV infection. Healthcare providers should prioritize vaccination efforts and employ a tailored approach to NAFLD in patients with prior viral hepatitis and especially HBV or HAV infection to limit disease-related outcomes.
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