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Corticosteroid plus glycyrrhizin therapy for chronic drug‐ or herb‐induced liver injury achieves biochemical and histological improvements: a randomised open‐label trial

Wang, Jia Bo; Huang, Ang; Wang, Yijin; Ji, Dong; Liang, Qing Sheng; Zhao, Jun; Zhou, Guangde; Liu, Shuhong; Niu, Ming; Sun, Ying; Tian, Hui; Teng, Guang Ju; Chang, Bin Xia; Bi, Jing Feng; Peng, Xiao Xia; Xin, Shaojie; Xie, Huan; Ma, Xiong; Mao, Yi Min; Liangpunsakul, Suthat; Saxena, Romil; Aithal, Guruprasad P.; Xiao, Xiao He; Zhao, Jingmin; Zou, Zhengsheng

Corticosteroid plus glycyrrhizin therapy for chronic drug‐ or herb‐induced liver injury achieves biochemical and histological improvements: a randomised open‐label trial Thumbnail


Authors

Jia Bo Wang

Ang Huang

Yijin Wang

Dong Ji

Qing Sheng Liang

Jun Zhao

Guangde Zhou

Shuhong Liu

Ming Niu

Ying Sun

Hui Tian

Guang Ju Teng

Bin Xia Chang

Jing Feng Bi

Xiao Xia Peng

Shaojie Xin

Huan Xie

Xiong Ma

Yi Min Mao

Suthat Liangpunsakul

Romil Saxena

Xiao He Xiao

Jingmin Zhao

Zhengsheng Zou



Abstract

Background
Treatment of chronic drug-induced liver injury (DILI) or herb-induced liver injury(HILI) is an important and unresolved challenge. There is no consensus regarding the indications for corticosteroids for chronic DILI/HILI.

Aims
To investigate the efficacy and safety of corticosteroid plus glycyrrhizin for patients with chronic DILI/HILI.

Methods
This was a randomised open-label trial. Eligible patients with causality assessment using the updated RUCAM were randomly assigned (1:1) either to the steroid treatment group (48-week stepwise dose reduction of methylprednisolone plus glycyrrhizin) or control group (glycyrrhizin alone). Liver biopsies were performed at baseline and at the end of the 48-week treatment period. The primary outcome was the proportion of patients with sustained biochemical response (SBR). The secondary outcomes were improvement in liver histology, time to biochemical normalisation and safety.

Results
Of 80 participants, 70 (87.5%) completed the trial. The patients were predominantly female (77.5%), aged >40 years (77.5%) and had a hepatocellular injury pattern of DILI (71.2%). Compared to the control group, the treatment group showed a higher proportion of SBR (94.3% vs. 71.4%, p = 0.023), shorter biochemical normalisation time and histological improvements in both histological activity and fibrosis. The DILI and HILI subgroups, as well as the autoimmune hepatitis (AIH)-like DILI and non-AIH-like subgroups, showed comparable responses. No severe adverse events were observed during the trial.

Conclusion
This study provides the first clinical evidence that corticosteroid plus glycyrrhizin therapy for chronic DILI with or without AIH-like features can achieve both biochemical response and histological improvements with good safety. (ClinicalTrials.gov, NCT 02651350).

Citation

Wang, J. B., Huang, A., Wang, Y., Ji, D., Liang, Q. S., Zhao, J., Zhou, G., Liu, S., Niu, M., Sun, Y., Tian, H., Teng, G. J., Chang, B. X., Bi, J. F., Peng, X. X., Xin, S., Xie, H., Ma, X., Mao, Y. M., Liangpunsakul, S., …Zou, Z. (2022). Corticosteroid plus glycyrrhizin therapy for chronic drug‐ or herb‐induced liver injury achieves biochemical and histological improvements: a randomised open‐label trial. Alimentary Pharmacology and Therapeutics, 55(10), 1297-1310. https://doi.org/10.1111/apt.16902

Journal Article Type Article
Acceptance Date Mar 13, 2022
Online Publication Date Mar 31, 2022
Publication Date 2022-05
Deposit Date Jun 30, 2023
Publicly Available Date Jul 17, 2023
Journal Alimentary Pharmacology and Therapeutics
Print ISSN 0269-2813
Electronic ISSN 1365-2036
Publisher Wiley
Peer Reviewed Peer Reviewed
Volume 55
Issue 10
Pages 1297-1310
DOI https://doi.org/10.1111/apt.16902
Keywords Drug-induced liver disease; glycyrrhizin; liver biopsy; herb-induced liver injury; methylprednisolone; randomised controlled trial; updated Roussel Uclaf causality assessment method (RUCAM)
Public URL https://nottingham-repository.worktribe.com/output/7834881
Publisher URL https://onlinelibrary.wiley.com/doi/10.1111/apt.16902

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