Efficacy and safety of AnluoHuaxian pills on chronic hepatitis B with normal or minimally elevated alanine transaminase and early liver fibrosis: A randomized controlled trial.

Chronic hepatitis B infection Histological change, AnluoHuaxian Liver fibrosis Randomized controlled trial Traditional Chinese medicine

Journal

Journal of ethnopharmacology
ISSN: 1872-7573
Titre abrégé: J Ethnopharmacol
Pays: Ireland
ID NLM: 7903310

Informations de publication

Date de publication:
15 Jul 2022
Historique:
received: 17 12 2021
revised: 07 02 2022
accepted: 16 03 2022
pubmed: 11 4 2022
medline: 18 5 2022
entrez: 10 4 2022
Statut: ppublish

Résumé

The AnluoHuaxian pill (AHP) is a widely used patented medicine for chronic hepatitis B (CHB) patients with advanced fibrosis or cirrhosis that has been used in China for more than 15 years. However, data are lacking on whether monotherapy with AHP can be effective in CHB patients with alanine aminotransferase (ALT) levels less than 2 times the upper limit of normal (ALT<2ULN) and early liver fibrosis (F ≤ 2). We aimed to investigate whether monotherapy with AHP improves liver histology in these patients. In this double-blind, randomized, placebo-controlled trial, 270 CHB patients with ALT<2ULN and F ≤ 2 were treated in 12 hospitals in China. The patients were randomly assigned to an intervention (AHP) group and a placebo group at a ratio of 2:1. Of these 270 enrolled patients, 147 had paired liver biopsies. The primary end point was histological change after 48 weeks of treatment. Per-protocol analysis revealed that the rate of histologic improvement in liver fibrosis patients in the AHP group was significantly higher than that in the placebo group (37.7% vs. 19.5%, P = 0.035) after 48 weeks of treatment, which was consistent with results from intention-to-treat and sensitivity analyses. Moreover, after adjusting for baseline characteristics, AHP was superior to placebo with respect to improving liver fibrosis (odds ratio [OR] = 2.58, 95% confidence interval [CI]: (1.01, 6.63),P = 0.049) and liver histology (OR = 3.62, 95% CI: (1.42, 9.20),P = 0.007). In noninvasive measurement of liver fibrosis (FibroScan®), the level of liver stiffness measurement (LSM) had decreased significantly at 48 weeks (5.1 kPa) compared with that at baseline (5.7 kPa) (P = 0.008) in the AHP group, whereas it did not decrease significantly in the placebo group. Cirrhosis developed in one patient in the placebo group but in no patients in the AHP group. No serious side effects occurred in the AHP-treated patients. Treatment of CHB patients who had ALT<2ULN and F ≤ 2 with the traditional Chinese medicine AHP for 48 weeks improves liver fibrosis. However, due to the short duration of treatment and the limited sample size of liver pathology, the long-term benefits of AHP in reducing fibrosis and the risk of cirrhosis and hepatocellular carcinoma in these patients need to be further studied in the future.

Identifiants

pubmed: 35398501
pii: S0378-8741(22)00249-5
doi: 10.1016/j.jep.2022.115210
pii:
doi:

Substances chimiques

Drugs, Chinese Herbal 0
anluohuaxian 0
Alanine Transaminase EC 2.6.1.2
Alanine OF5P57N2ZX

Types de publication

Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

115210

Informations de copyright

Copyright © 2022 The Authors. Published by Elsevier B.V. All rights reserved.

Auteurs

Huan-Ming Xiao (HM)

Hepatology Department, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangdong Provincial Hospital of Chinese Medicine, Guangzhou, 510120, China.

Mei-Jie Shi (MJ)

Hepatology Department, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangdong Provincial Hospital of Chinese Medicine, Guangzhou, 510120, China.

Jun-Min Jiang (JM)

Hepatology Department, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangdong Provincial Hospital of Chinese Medicine, Guangzhou, 510120, China.

Gao-Shu Cai (GS)

Hepatology Department, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangdong Provincial Hospital of Chinese Medicine, Guangzhou, 510120, China.

Yu-Bao Xie (YB)

Hepatology Department, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangdong Provincial Hospital of Chinese Medicine, Guangzhou, 510120, China.

Guang-Jun Tian (GJ)

Hepatology Department, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangdong Provincial Hospital of Chinese Medicine, Guangzhou, 510120, China.

Jing-Dong Xue (JD)

Liver Diseases Branch, Shaanxi Provincial Hospital of Traditional Chinese Medicine, Xi'an, 710003, China.

De-Wen Mao (DW)

Hepatology Department, First Affiliated Hospital of Guangxi University of Traditional Chinese Medicine, Nanning, 530023, China.

Qin Li (Q)

Department of Integration of Traditional Chinese and Western Medicine, Mengchao Hepatobiliary Hospital of Fujian Medical University, Fuzhou, 350025, China.

Hong-Zhi Yang (HZ)

Chinese Medicine Department, Third Affiliated Hospital, SunYat-Sen University, Guangzhou, 510630, China.

Hui Guo (H)

Hepatology Department, First Teaching Hospital of Tianjin University of Traditional Chinese Medicine, Tianjin, 300380, China.

Chun-Liang Lei (CL)

Hepatology Department, Guangzhou Eighth People's Hospital, Guangzhou, 510060, China.

Wei Lu (W)

Liver Diseases Branch, Tianjin Second People's Hospital, Tianjin, 300192, China.

Liang Chen (L)

Department of Hepatology, Shanghai Public Health Clinical Center, Shanghai, 201508, China.

Hua-Bao Liu (HB)

Hepatology Department, Chongqing Hospital of Traditional Chinese Medicine, Chongqing, 400021, China.

Jing Wang (J)

Department of Hepatobiliary Disease, Affiliated Traditional Chinese Medicine Hospital of Southwest Medical University, Luzhou, 646000, China.

Yue-Qiu Gao (YQ)

Department of Hepatopathy, Shuguang Hospital, Affiliated to Shanghai University of Traditional Chinese Medicine, Shanghai, 201203, China.

Jie-Zhen Chen (JZ)

Hepatology Department, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangdong Provincial Hospital of Chinese Medicine, Guangzhou, 510120, China.

Shu-Duo Wu (SD)

Hepatology Department, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangdong Provincial Hospital of Chinese Medicine, Guangzhou, 510120, China.

Hui-Jun Chen (HJ)

Hepatology Department, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangdong Provincial Hospital of Chinese Medicine, Guangzhou, 510120, China.

Peng-Tao Zhao (PT)

Hepatology Department, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangdong Provincial Hospital of Chinese Medicine, Guangzhou, 510120, China.

Chao-Zhen Zhang (CZ)

Hepatology Department, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangdong Provincial Hospital of Chinese Medicine, Guangzhou, 510120, China.

Wen-Wei Ou-Yang (WW)

Key Unit of Methodology in Clinical Research, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangdong Provincial Hospital of Chinese Medicine, Guangzhou, 510120, China.

Ze-Huai Wen (ZH)

Key Unit of Methodology in Clinical Research, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangdong Provincial Hospital of Chinese Medicine, Guangzhou, 510120, China; National Centre for Design Measurement and Evaluation in Clinical Research, Guangzhou University of Chinese Medicine, Guangzhou, 510405, China. Electronic address: wenzh@gzucm.edu.cn.

Xiao-Ling Chi (XL)

Hepatology Department, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangdong Provincial Hospital of Chinese Medicine, Guangzhou, 510120, China. Electronic address: bdxgy@gzucm.edu.cn.

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