• Medientyp: E-Artikel
  • Titel: ALT Levels in Treatment-Naive, Chronic Hepatitis B Patients with Concurrent Fatty Liver Disease: A US Nationwide Study
  • Beteiligte: Chang, Christine Y.; Kam, Leslie; Dang, Nolan; Cheung, Ramsey; Nguyen, Mindie H.
  • Erschienen: S. Karger AG, 2022
  • Erschienen in: Digestive Diseases, 40 (2022) 4, Seite 497-505
  • Sprache: Englisch
  • DOI: 10.1159/000518645
  • ISSN: 0257-2753; 1421-9875
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  • Beschreibung: <b><i>Introduction:</i></b> Treatment criteria for chronic hepatitis B (CHB) relies on ALT, which can be impacted by concurrent nonalcoholic fatty liver disease (NAFLD), but ALT data on patients with CHB and NAFLD are limited. We aimed to characterize ALT distribution in untreated CHB patients with NAFLD. <b><i>Methods:</i></b> We retrospectively analyzed untreated US adults with CHB (533 with NAFLD, 3,172 without NAFLD) using the Clinformatics<sup>™</sup> Data Mart Database (2003–2019). The main outcome was ALT elevation (>1× upper limit of normal, 35/25 U/L for men/women, respectively). Secondary outcomes were advanced fibrosis (via FIB-4 index) and factors associated with fibrosis. <b><i>Results:</i></b> The majority of patients were Asian (61.0%) and hepatitis B e-antigen (HBeAg)-negative (90.4%). Patients with CHB and NAFLD were older (57.2 vs. 49.5 years, <i>p</i> < 0.001), more likely male (59.3% vs. 46.2%, <i>p</i> < 0.001), with higher percentages of advanced fibrosis (3.6% vs. 2.6%, <i>p</i> < 0.001) than those with CHB alone. CHB-NAFLD patients were more likely to have elevated ALT than those with CHB only, but this difference was only significant among those with low hepatitis B virus (HBV) DNA (38.1% vs. 25.6%, <i>p</i> < 0.001), not those with higher HBV DNA (>2,000 IU/mL). After adjusting for HBeAg, HBV DNA, and diabetes, NAFLD was not independently associated with advanced fibrosis (odds ratio 1.18, 95% confidence interval: 0.30–4.59, <i>p</i> = 0.81). <b><i>Discussion:</i></b> CHB-NAFLD patients with HBV DNA below treatment threshold were more likely to have elevated ALT but not those with higher HBV DNA, suggesting that ALT threshold does not need to be raised for antiviral eligibility for CHB with NAFLD.