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  1. Article: 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

    Xiao, Huan-Ming / Shi, Mei-Jie / Jiang, Jun-Min / Cai, Gao-Shu / Xie, Yu-Bao / Tian, Guang-Jun / Xue, Jing-Dong / Mao, De-Wen / Li, Qin / Yang, Hong-Zhi / Guo, Hui / Lei, Chun-Liang / Lu, Wei / Chen, Liang / Liu, Hua-Bao / Wang, Jing / Gao, Yue-Qiu / Chen, Jie-Zhen / Wu, Shu-Duo /
    Chen, Hui-Jun / Zhao, Peng-Tao / Zhang, Chao-Zhen / Ou-Yang, Wen-Wei / Wen, Ze-Huai / Chi, Xiao-Ling

    Journal of ethnopharmacology. 2022 Mar. 16,

    2022  

    Abstract: The AnluoHuaxian pill (AHP) is a widely used patented medicine for chronic hepatitis B (CHB) patients withadvanced fibrosis or cirrhosisthat has been used in China for more than 15 years. However, data are lacking on whether monotherapy with AHP can be ... ...

    Abstract The AnluoHuaxian pill (AHP) is a widely used patented medicine for chronic hepatitis B (CHB) patients withadvanced fibrosis or cirrhosisthat 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.
    Keywords Oriental traditional medicine ; alanine transaminase ; chronic hepatitis B ; confidence interval ; fibrosis ; hepatoma ; histology ; liver ; liver cirrhosis ; odds ratio ; patents ; patients ; placebos ; randomized clinical trials ; risk ; sample size ; China
    Language English
    Dates of publication 2022-0316
    Publishing place Elsevier B.V.
    Document type Article
    Note Pre-press version
    ZDB-ID 134511-4
    ISSN 1872-7573 ; 0378-8741
    ISSN (online) 1872-7573
    ISSN 0378-8741
    DOI 10.1016/j.jep.2022.115210
    Database NAL-Catalogue (AGRICOLA)

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  2. Article ; Online: 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.

    Xiao, Huan-Ming / Shi, Mei-Jie / Jiang, Jun-Min / Cai, Gao-Shu / Xie, Yu-Bao / Tian, Guang-Jun / Xue, Jing-Dong / Mao, De-Wen / Li, Qin / Yang, Hong-Zhi / Guo, Hui / Lei, Chun-Liang / Lu, Wei / Chen, Liang / Liu, Hua-Bao / Wang, Jing / Gao, Yue-Qiu / Chen, Jie-Zhen / Wu, Shu-Duo /
    Chen, Hui-Jun / Zhao, Peng-Tao / Zhang, Chao-Zhen / Ou-Yang, Wen-Wei / Wen, Ze-Huai / Chi, Xiao-Ling

    Journal of ethnopharmacology

    2022  Volume 293, Page(s) 115210

    Abstract: Ethnopharmacological relevance: 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 ... ...

    Abstract Ethnopharmacological relevance: 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).
    Aim of the study: We aimed to investigate whether monotherapy with AHP improves liver histology in these patients.
    Materials and methods: 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.
    Results: 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.
    Conclusions: 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.
    MeSH term(s) Alanine/therapeutic use ; Alanine Transaminase ; Drugs, Chinese Herbal ; Hepatitis B, Chronic/drug therapy ; Humans ; Liver/pathology ; Liver Cirrhosis/drug therapy ; Liver Cirrhosis/pathology
    Chemical Substances Drugs, Chinese Herbal ; anluohuaxian ; Alanine Transaminase (EC 2.6.1.2) ; Alanine (OF5P57N2ZX)
    Language English
    Publishing date 2022-04-07
    Publishing country Ireland
    Document type Journal Article ; Randomized Controlled Trial
    ZDB-ID 134511-4
    ISSN 1872-7573 ; 0378-8741
    ISSN (online) 1872-7573
    ISSN 0378-8741
    DOI 10.1016/j.jep.2022.115210
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Protocol of a prospective study for the combination treatment of Shu-Gan-jian-Pi decoction and steroid standard therapy in autoimmune hepatitis patients.

    Chi, Xiao-Ling / Xiao, Huan-Ming / Xie, Yu-Bao / Cai, Gao-Shu / Jiang, Jun-Min / Tian, Guang-Jun / Shi, Mei-Jie / Wu, Shu-Duo / Zhao, Peng-Tao / Chen, Hui-Jun

    BMC complementary and alternative medicine

    2016  Volume 16, Issue 1, Page(s) 505

    Abstract: Background: Prednisone plus azathioprine is considered the mainstay of therapy in the current recommendations for autoimmune hepatitis (AIH). However, it does not provide good benefits for AIH patients because of its serious side effects. Therefore, ... ...

    Abstract Background: Prednisone plus azathioprine is considered the mainstay of therapy in the current recommendations for autoimmune hepatitis (AIH). However, it does not provide good benefits for AIH patients because of its serious side effects. Therefore, more and more AIH patients prefer to seek for traditional Chinese medicine (TCM) to manage their symptoms and reduce the side effects of steroids in China. Shu-Gan-Jian-Pi Decoction is a popular used Chinese herbal formula in Guangdong province of China, which has demonstrated the effect of improving efficacy and reducing side effects of corticosteroids in AIH patients. The aim of this study is to evaluate the effects of Shu-Gan-Jian-Pi Decoction combined with steroid in AIH patients. So, this study aims to explore whether the combination treatment of Shu-Gan-Jian-Pi Decoction and steroid standard therapy could improve the clinical management of AIH.
    Methods: A prospective non-randomized study on AIH will be conducted between October 2015 and June 2017 in Guangdong Provincial hospital of Chinese medicine. Eligible AIH patients will be classified as the case group (n = 66) and the control group (n = 66) based on the interventions. Patients taking Shu-Gan-Jian-Pi Decoction combined with prednisone and azathioprine will be in the case group and those taking prednisone and azathioprine will be in the control group. The whole study will last 48 weeks, including a 24-week observation period and a 24-week follow-up period. The primary outcome was complete response to therapy, defined as complete biochemical remission at the patient's last visit of observation period and the absence of predefined steroid-specific side effects throughout treatment.
    Discussion: This trial will evaluate the efficacy and safety of Shu-Gan-Jian-Pi Decoction combined with prednisone and azathioprine on AIH patients. The achievement of this trial will provide evidence-based data for Shu-Gan-Jian-Pi Decoction, which could provide good benefits for AIH patients.
    Trial registration: Chinese Clinical Trial Registry: ChiCTR-OOC-15006155 . Registration date: 28 March 2015.
    MeSH term(s) Azathioprine/therapeutic use ; Clinical Protocols ; Drugs, Chinese Herbal/pharmacology ; Drugs, Chinese Herbal/therapeutic use ; Glucocorticoids/therapeutic use ; Hepatitis, Autoimmune/drug therapy ; Humans ; Immunosuppressive Agents/therapeutic use ; Prednisone/therapeutic use ; Prospective Studies
    Chemical Substances Drugs, Chinese Herbal ; Glucocorticoids ; Immunosuppressive Agents ; shu-gan-jian-pi ; Azathioprine (MRK240IY2L) ; Prednisone (VB0R961HZT)
    Language English
    Publishing date 2016-12-07
    Publishing country England
    Document type Controlled Clinical Trial ; Journal Article
    ZDB-ID 2050429-9
    ISSN 1472-6882 ; 1472-6882
    ISSN (online) 1472-6882
    ISSN 1472-6882
    DOI 10.1186/s12906-016-1486-1
    Database MEDical Literature Analysis and Retrieval System OnLINE

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