肝豆灵通过调节肠道菌群改善肝纤维化:一项随机、双盲、安慰剂对照试验。

IF 2.9 Q3 MICROBIOLOGY
Bioscience of microbiota, food and health Pub Date : 2025-01-01 Epub Date: 2025-06-09 DOI:10.12938/bmfh.2025-012
Yue Pu, Rui Li, Hong Chen, Ying Ma, Hao Ye, Xinxiang Zhang, Juan Zhang
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引用次数: 0

摘要

本研究基于肝纤维触摸技术结合16S rRNA基因测序技术,旨在探讨肝豆灵(GDL)改善威尔逊病(Wilson’s disease, WD)后肝纤维化指标及肠道菌群的变化。选择安徽省中医院脑病中心收治的WD型肝纤维化患者90例,随机分为观察组和对照组,进行48天的随机、双盲、安慰剂对照试验。两组患者均给予常规二巯基丙磺酸钠治疗,观察组患者在常规治疗的基础上加用GDL,对照组患者给予相应的安慰剂治疗。治疗前后评估肝脏僵硬度,采集血液样本进行实验室检测,采集粪便样本进行16S rRNA测序。补充GDL可显著改善肝脏硬度和非侵袭性肝纤维化建模指标,同时丙氨酸转氨酶、天冬氨酸转氨酶、γ -谷氨酰转氨酶、胆汁酸、血小板、透明质酸和层粘连蛋白水平也显著提高(p
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Gandouling improves Wilson's disease liver fibrosis by modulating intestinal flora: a randomized, double-blind, placebo-controlled trial.

Gandouling improves Wilson's disease liver fibrosis by modulating intestinal flora: a randomized, double-blind, placebo-controlled trial.

Gandouling improves Wilson's disease liver fibrosis by modulating intestinal flora: a randomized, double-blind, placebo-controlled trial.

Gandouling improves Wilson's disease liver fibrosis by modulating intestinal flora: a randomized, double-blind, placebo-controlled trial.

Based on liver FibroTouch technology combined with 16S rRNA gene sequencing technology, this study aimed to explore the changes of liver fibrosis indexes and intestinal flora in Wilson's disease (WD) improved by Gandouling (GDL). Ninety patients with WD hepatic fibrosis at the Brain Disease Center of the Anhui Provincial Hospital of Traditional Chinese Medicine were included and randomly divided into an observation group and a control group for a 48-day randomized, double-blind, placebo-controlled trial. Patients in both groups were treated with conventional sodium dimercaptopropanesulfonate, to which GDL was added in the observation group, while the control group was given the corresponding placebo treatment. Before and after treatment, liver stiffness was assessed, blood samples were collected for laboratory tests, and stool samples were collected for 16S rRNA sequencing. Supplementation with GDL significantly improved liver stiffness and non-invasive liver fibrosis modeling indicators, while alanine aminotransferase, aspartate aminotransferase, gamma-glutamyltransferase, bile acid, platelets, hyaluronic acid and laminin levels were also significantly improved (p<0.05). Other parameters showed no significant changes. The results of intestinal microbial testing showed that the microbial diversity and composition of the patients in the observation group underwent significant optimization, in which the number of probiotics rose but the number of pathogenic and opportunistic pathogens declined and even basically returned to the normal range. GDL combined with conventional liver-protecting and copper-removing treatments can effectively improve patients' liver fibrosis-related indexes. Furthermore, GDL has the ability to regulate the composition and diversity of the intestinal flora and promote reconstruction of the intestinal microbial community, which in turn may reverse the state of hepatic fibrosis.

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