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Fatty liver is not independently associated with the rates of complete response to oral antiviral therapy in chronic hepatitis B patients.
Li, Jie; Le, An K; Chaung, Kevin T; Henry, Linda; Hoang, Joseph K; Cheung, Ramsey; Nguyen, Mindie H.
Affiliation
  • Li J; Department of Infectious Disease, Shandong Provincial Hospital Affiliated to Shandong University, Ji'nan, Shandong, China.
  • Le AK; Division of Gastroenterology and Hepatology, Stanford University Medical Center, Stanford, CA, USA.
  • Chaung KT; Division of Gastroenterology and Hepatology, Stanford University Medical Center, Stanford, CA, USA.
  • Henry L; Division of Gastroenterology and Hepatology, Stanford University Medical Center, Stanford, CA, USA.
  • Hoang JK; Division of Gastroenterology and Hepatology, Stanford University Medical Center, Stanford, CA, USA.
  • Cheung R; Division of Gastroenterology and Hepatology, Stanford University Medical Center, Stanford, CA, USA.
  • Nguyen MH; Division of Gastroenterology and Hepatology, Stanford University Medical Center, Stanford, CA, USA.
Liver Int ; 40(5): 1052-1061, 2020 05.
Article in En | MEDLINE | ID: mdl-32086988
ABSTRACT
BACKGROUND &

AIMS:

Nonalcoholic fatty liver disease (NAFLD) and chronic hepatitis B (CHB) are common liver diseases. Concurrent NAFLD may affect antiviral treatment outcomes in CHB patients. The aim of this study is to investigate the impact of NAFLD on complete viral suppression ([CVS], HBV DNA <20-100 IU/mL) and/or biochemical response ([BR], ALT of ≤25 U/L for females; 35 U/L for males) in CHB patients who received oral antiviral therapy.

METHODS:

A retrospective study of 555 treated CHB patients (187 NAFLD; 368 non-NAFLD) from 2000 to 2016 at a USA medical centre. NAFLD was diagnosed by imaging and/or histology after ruling out secondary causes of hepatic steatosis.

RESULTS:

The majority of patients were male (60.7%), Asian (87.56%) and HBeAg-negative (66.7%). NAFLD patients compared to non-NAFLD were more likely HBeAg negative (74.3% vs 62.8%, P = .02), hypertensive (33.2% vs 22.8%, P = .009) and male (67.4% vs 57.3%, P = .02) with a higher mean BMI (25.4 ± 4.3 vs 23.8 ± 4.0 kg/m2 , P < .001). Both cohorts achieved similar rates of CVS (86% vs 88%) and BR (38% vs 41%) during the follow-up of up to 60 months (P > .05), but NAFLD had higher cumulative rates of CVS + BR, compared with non-NAFLD patients (32.5% vs 22.8%, P = .03). In multivariate analyses, NAFLD was not independently associated with CVS and/or BR outcomes. Receipt of entecavir or tenofovir (vs older therapies) and lower baseline HBV DNA or higher ALT were positively associated with achieving CVS or BR.

CONCLUSION:

Concomitant NAFLD had no impact on the long-term rates of CVS and/or BR in treated CHB patients.
Subject(s)
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hepatitis B, Chronic / Non-alcoholic Fatty Liver Disease Type of study: Observational_studies / Risk_factors_studies Limits: Female / Humans / Male Language: En Journal: Liver Int Journal subject: GASTROENTEROLOGIA Year: 2020 Document type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hepatitis B, Chronic / Non-alcoholic Fatty Liver Disease Type of study: Observational_studies / Risk_factors_studies Limits: Female / Humans / Male Language: En Journal: Liver Int Journal subject: GASTROENTEROLOGIA Year: 2020 Document type: Article Affiliation country: China