Literature DB >> 30890501

[Association of baseline alanine aminotransferase levels with therapeutic effects of entecavir and interferon-α in patients with chronic hepatitis B].

Zhiqi Xiao1, Fuyuan Zhou1, Bin Zhou1, Jie Yang1.   

Abstract

OBJECTIVE: To evaluate the therapeutic effects of entecavir (ETV) and interferon-α (IFN-α) treatments for 48 weeks for chronic hepatitis B (CHB) in patients with different baseline alanine aminotransferase (ALT) levels.
METHODS: We retrospectively analyzed the data of 369 CHB patients receiving ETV and IFN-α treatments for 48 weeks. We compared the virological response rates, HBsAg clearance, and HBsAg reduction between the patients receiving ETV and IFN-α treatments with different baseline ALT levels[≤ 5×upper limits of normal (ULN) level (subgroup 1), 5-10×ULN (subgroup 2), and > 10× ULN (subgroup 3)].
RESULTS: In patients receiving ETV treatment, the virological response rate was 83.3% in subgroup 1, 91.4% in subgroup 2, and 95.5% in subgroup 3, as compared with 19.7%, 40%, and 42.9% in the 3 subgroups with IFN-α treatment, respectively, showing significantly differences both among different subgroups with the same treatment and between the same subgroup with different treatments (P < 0.05). HBeAg clearance rates in the 3 subgroups were 8.3%, 16.7% and 35.5% in patients with ETV treatment and were 1.8%, 41.9%, and 38.1% in patients with IFN-α treatment, respectively, showing significant differences among the 3 subgroups with the same treatment (P < 0.05); in the same subgroups with different treatments, the rates differed significantly only between subgroups 2 (P < 0.05). In ETV group, the rate of HBsAg reduction to below 200 IU/ml was 2.5% in subgroup 1 and 13.8% in subgroup 2, showing no significant difference between the two subgroups; in IFN-α group, the rates were also similar between subgroups 1 and 2 (30.6% vs 33.3%, P > 0.05); but the rates differed significantly between the same subgroups with different treatments (P < 0.05).
CONCLUSIONS: In all the subgroups with different baseline ALT levels, ETV treatment for 48 weeks results in significantly higher virological response rates than IFN-α treatment in patients with CHB. In patients with a baseline ALT of 5-10 ×ULN, IFN-α can result in a higher HBeAg clearance rate than ETV. In patients with comparable baseline ALT level, IFN-α more effectively reduces HBsAg level than ETV. The patients with a relatively high baseline ALT level (> 5 × ULN) show better responses to both ETV and IFN-α treatment than those with ALT level below 5×ULN. We thus recommend IFN-α for patients with a baseline ALT of 5-10×ULN and ETV for patients with a baseline ALT either below 5 × ULN or beyond 10×ULN.

Entities:  

Keywords:  alanine aminotransferase; chronic hepatitis B; entecavir; interferon-α

Mesh:

Substances:

Year:  2019        PMID: 30890501      PMCID: PMC6765642          DOI: 10.12122/j.issn.1673-4254.2019.09.04

Source DB:  PubMed          Journal:  Nan Fang Yi Ke Da Xue Xue Bao        ISSN: 1673-4254


  24 in total

1.  A baseline tool for predicting response to peginterferon alfa-2a in HBeAg-positive patients with chronic hepatitis B.

Authors:  H L Y Chan; D Messinger; G V Papatheodoridis; M Cornberg; Q Xie; T Piratvisuth; H Ren; P T Kennedy; A Thompson; A Caputo; G Bakalos; V Pavlovic; P Lampertico
Journal:  Aliment Pharmacol Ther       Date:  2018-06-29       Impact factor: 8.171

2.  Quantification of HBsAg in nucleos(t)ide-naïve patients treated for chronic hepatitis B with entecavir with or without tenofovir in the BE-LOW study.

Authors:  Fabien Zoulim; Giampiero Carosi; Susan Greenbloom; Wlodzimierz Mazur; Tuan Nguyen; Lennox Jeffers; Maurizia Brunetto; Song Yu; Cyril Llamoso
Journal:  J Hepatol       Date:  2014-08-28       Impact factor: 25.083

3.  Patients with chronic hepatitis B treated with oral antiviral therapy retain a higher risk for HCC compared with patients with inactive stage disease.

Authors:  Ju-Yeon Cho; Yong-Han Paik; Won Sohn; Hyun Chin Cho; Geum-Youn Gwak; Moon Seok Choi; Joon Hyeok Lee; Kwang Cheol Koh; Seung Woon Paik; Byung Chul Yoo
Journal:  Gut       Date:  2014-03-10       Impact factor: 23.059

Review 4.  Chronic hepatitis B therapy: available drugs and treatment guidelines.

Authors:  G P Caviglia; M L Abate; R Pellicano; A Smedile
Journal:  Minerva Gastroenterol Dietol       Date:  2014-10-17

Review 5.  Hepatitis B: encouraging the use of interferon.

Authors:  Thinesh Lee Krishnamoorthy; David Mutimer
Journal:  Curr Opin Infect Dis       Date:  2015-12       Impact factor: 4.915

6.  Long-term efficacy of interferon alpha therapy on hepatitis B viral replication in patients with chronic hepatitis B: a meta-analysis.

Authors:  Yong-Feng Yang; Wei Zhao; Hai-Ming Xia; Yan-Dan Zhong; Ping Huang; Jian Wen
Journal:  Antiviral Res       Date:  2009-11-10       Impact factor: 5.970

7.  Peginterferon Is Superior to Nucleos(t)ide Analogues for Prevention of Hepatocellular Carcinoma in Chronic Hepatitis B.

Authors:  Kung-Hao Liang; Chao-Wei Hsu; Ming-Ling Chang; Yi-Cheng Chen; Ming-Wei Lai; Chau-Ting Yeh
Journal:  J Infect Dis       Date:  2015-11-17       Impact factor: 5.226

Review 8.  Personalized treatment of hepatitis B.

Authors:  Anna S Lok
Journal:  Clin Mol Hepatol       Date:  2015-03-25

9.  Entecavir treatment does not eliminate the risk of hepatocellular carcinoma in chronic hepatitis B: limited role for risk scores in Caucasians.

Authors:  Pauline Arends; Milan J Sonneveld; Roeland Zoutendijk; Ivana Carey; Ashley Brown; Massimo Fasano; David Mutimer; Katja Deterding; Jurriën G P Reijnders; Ye Oo; Jörg Petersen; Florian van Bömmel; Robert J de Knegt; Teresa Santantonio; Thomas Berg; Tania M Welzel; Heiner Wedemeyer; Maria Buti; Pierre Pradat; Fabien Zoulim; Bettina Hansen; Harry L A Janssen
Journal:  Gut       Date:  2014-07-10       Impact factor: 23.059

10.  Efficacy Comparison of Tenofovir and Entecavir in HBeAg-Positive Chronic Hepatitis B Patients with High HBV DNA.

Authors:  Hong Shi; Mingxing Huang; Guoli Lin; Xiangyong Li; Yuankai Wu; Yusheng Jie; Yutian Chong
Journal:  Biomed Res Int       Date:  2016-03-01       Impact factor: 3.411

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.