Viral Hepatitis
Copyright ©The Author(s) 2002. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Aug 15, 2002; 8(4): 679-685
Published online Aug 15, 2002. doi: 10.3748/wjg.v8.i4.679
Clinical observation of salvianolic acid B in treatment of liver fibrosis in chronic hepatitis B
Ping Liu, Yi-Yang Hu, Cheng Liu, Da-Yuan Zhu, Hui-Ming Xue, Zhi-Qiang Xu, Lie- Ming Xu, Cheng-Hai Liu, Hong-Tu Gu, Zhi-Qing Zhang
Ping Liu, Yi-Yang Hu, Cheng Liu, Hui-Ming Xue, Zhi-Qiang Xu, Lie- Ming Xu, Cheng-Hai Liu, Hong-Tu Gu, Shanghai University of Traditional Chinese Medicine, Shanghai 200032, China
Da-Yuan Zhu, Shanghai Institute of Metaria Medica, Chinese Academy of Sciences, Shanghai 200031, China
Zhi-Qing Zhang, the 4th Huaiyin City Hospital, Huaian City, 223000, JiangSu Province, China
Author contributions: All authors contributed equally to the work.
Supported by the National 9th Five-Year Breakthrough Scientific Project, No.96-906-08-02
Correspondence to: Dr. Ping Liu, Professor of medicine, Shanghai University of Traditional Chinese Medicine Institute of Liver Diseases, 530 LingLing Rd, Shanghai 200032, China. liuliver@online.sh.cn
Telephone: +86-21-5423-1109 Fax: +86-21-6403-6889
Received: October 21, 2001
Revised: December 12, 2001
Accepted: December 20, 2001
Published online: August 15, 2002
Abstract

AIM: To evaluate the clinical efficacy of salvianolic acid B (SA-B) on liver fibrosis in chronic hepatitis B.

METHODS: Sixty patients with definite diagnosis of liver fibrosis with hepatitis B were included in the trial. Interferon-γ (IFN-γ) was used as control drug. The patients took orally SA-B tablets or received muscular injection of IFN-γ in the double blind randomized test. The complete course lasted 6 mo. The histological changes of liver biopsy specimen before and after the treatment were the main evidence in evaluation, in combination with the results of contents of serum HA, LN, IV-C, P-III-P, liver ultrasound imaging, and symptoms and signs.

RESULTS: Reverse rate of fibrotic stage was 36.67% in SA-B group and 30.0% in IFN-γ group. Inflammatory alleviating rate was 40.0% in SA-B group and 36.67% in IFN-γ group. The average content of HA and IV-C was significantly lower than that before treatment. The abnormal rate also decreased remarkably. Overall analysis of 4 serological fibrotic markers showed significant improvement in SA-B group as compared with the IFN-γ group. Score of liver ultrasound imaging was lower in SA-B group than in IFN-γ group (HA 36.7% vs 80%, IV-C 3.3% vs 23.2%). Before the treatment, ALT AST activity and total bilirubin content of patients who had regression of fibrosis after oral administration of SA-B, were significantly lower than those of patients who had aggravation of fibrosis after oral administration of SA-B. IFN-γ showed certain side effects (fever and transient decrease of leukocytes, occurrence rates were 50% and 3.23%), but SA-B showed no side effects.

CONCLUSION: SA-B could effectively reverse liver fibrosis in chronic hepatitis B. SA-B was better than IFN-γ in reduction of serum HA content, overall decrease of 4 serum fibrotic markers, and decrease of ultrasound imaging score. Liver fibrosis in chronic hepatitis B with slight liver injury was more suitable to SA-B in anti-fibrotic treatment. SA-B showed no obvious side effects.

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