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Intestinal microbiota in the treatment of metabolically associated fatty liver disease
1Shanxi Medical University, Taiyuan 030001, Shanxi Province, China.
Abstract:
Metabolically associated fatty liver disease (MAFLD) is a common cause of chronic liver disease, the hepatic manifestation of metabolic syndrome. Despite the increasing incidence of MAFLD, no effective treatment is available. Recent research indicates a link between the intestinal microbiota and liver diseases such as MAFLD. The composition and characteristics of the intestinal microbiota and therapeutic perspectives of MAFLD are reviewed in the current study. An imbalance in the intestinal microbiota increases intestinal permeability and exposure of the liver to adipokines. Furthermore, we focused on reviewing the latest "gut-liver axis" targeted therapy.
Insights
Metabolically associated fatty liver disease (MAFLD), linked to metabolic syndrome, lacks effective treatments. This review explores how gut microbiota imbalances impact MAFLD and discusses emerging gut-liver axis therapies.
Area of Science:
- Hepatology
- Gastroenterology
- Microbiology
Background:
- Metabolically associated fatty liver disease (MAFLD) is a prevalent hepatic manifestation of metabolic syndrome.
- The increasing incidence of MAFLD highlights the urgent need for effective therapeutic strategies.
- Emerging evidence suggests a significant role for the intestinal microbiota in the pathogenesis of liver diseases, including MAFLD.
Purpose of the Study:
- To review the current understanding of the intestinal microbiota's composition and characteristics in MAFLD.
- To explore the therapeutic perspectives targeting the gut-liver axis for MAFLD treatment.
- To synthesize recent research on the gut-liver axis in the context of MAFLD.
Main Methods:
- Comprehensive literature review of studies investigating the gut-liver axis and MAFLD.
- Analysis of research on intestinal microbiota alterations in MAFLD patients.
- Evaluation of emerging therapeutic strategies targeting gut microbiota and the gut-liver axis.
Main Results:
- Dysbiosis of the intestinal microbiota contributes to increased intestinal permeability.
- Increased intestinal permeability leads to elevated liver exposure to adipokines, exacerbating MAFLD.
- The gut-liver axis presents a promising target for novel MAFLD therapies.
Conclusions:
- The intestinal microbiota plays a critical role in the development and progression of MAFLD.
- Targeting the gut-liver axis offers a potential therapeutic avenue for MAFLD.
- Further research into gut-targeted therapies is warranted for effective MAFLD management.
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