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微生物群和免疫系统在代谢功能障碍相关脂肪性肝病发生和进展中的作用。

Implications of Microbiota and Immune System in Development and Progression of Metabolic Dysfunction-Associated Steatotic Liver Disease.

机构信息

Boston Combined Residency Program, Boston Children's Hospital & Boston Medical Center, Boston, MA 02115, USA.

College of Medicine and Health, University College Cork, T12 YN60 Cork, Ireland.

出版信息

Nutrients. 2024 May 29;16(11):1668. doi: 10.3390/nu16111668.


DOI:10.3390/nu16111668
PMID:38892602
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11175128/
Abstract

Metabolic dysfunction-associated steatotic liver disease (MASLD) is the most prevalent type of liver disease worldwide. The exact pathophysiology behind MASLD remains unclear; however, it is thought that a combination of factors or "hits" act as precipitants for disease onset and progression. Abundant evidence supports the roles of diet, genes, metabolic dysregulation, and the intestinal microbiome in influencing the accumulation of lipids in hepatocytes and subsequent progression to inflammation and fibrosis. Currently, there is no cure for MASLD, but lifestyle changes have been the prevailing cornerstones of management. Research is now focusing on the intestinal microbiome as a potential therapeutic target for MASLD, with the spotlight shifting to probiotics, antibiotics, and fecal microbiota transplantation. In this review, we provide an overview of how intestinal microbiota interact with the immune system to contribute to the pathogenesis of MASLD and metabolic dysfunction-associated steatohepatitis (MASH). We also summarize key microbial taxa implicated in the disease and discuss evidence supporting microbial-targeted therapies in its management.

摘要

代谢相关脂肪性肝病(MASLD)是全球最常见的肝病类型。MASLD 的确切病理生理学机制尚不清楚;然而,人们认为多种因素或“打击”共同作用作为疾病发作和进展的诱因。大量证据支持饮食、基因、代谢失调和肠道微生物组在影响肝细胞内脂质堆积以及随后发展为炎症和纤维化中的作用。目前,MASLD 尚无治愈方法,但生活方式改变一直是管理的主要基石。目前的研究重点是肠道微生物组作为 MASLD 的潜在治疗靶点,研究重点转向益生菌、抗生素和粪便微生物群移植。在这篇综述中,我们概述了肠道微生物组如何与免疫系统相互作用,从而导致 MASLD 和代谢相关脂肪性肝炎(MASH)的发病机制。我们还总结了与疾病相关的关键微生物类群,并讨论了支持其管理中针对微生物的治疗方法的证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8a7/11175128/683ed7505b6c/nutrients-16-01668-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8a7/11175128/683ed7505b6c/nutrients-16-01668-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8a7/11175128/683ed7505b6c/nutrients-16-01668-g001.jpg

相似文献

[1]
Implications of Microbiota and Immune System in Development and Progression of Metabolic Dysfunction-Associated Steatotic Liver Disease.

Nutrients. 2024-5-29

[2]
Nutritional Interventions, Probiotics, Synbiotics and Fecal Microbiota Transplantation in Steatotic Liver Disease : Pediatric Fatty Liver and Probiotics.

Adv Exp Med Biol. 2024

[3]
Gut microbial metabolites in MASLD: Implications of mitochondrial dysfunction in the pathogenesis and treatment.

Hepatol Commun. 2024-7-1

[4]
Probiotic Mixture Ameliorates a Diet-Induced MASLD/MASH Murine Model through the Regulation of Hepatic Lipid Metabolism and the Gut Microbiome.

J Agric Food Chem. 2024-4-17

[5]
Gut microbiota-NLRP3 inflammasome crosstalk in metabolic dysfunction-associated steatotic liver disease.

Clin Res Hepatol Gastroenterol. 2024-10

[6]
Alteration of Gut Microbiota Composition in the Progression of Liver Damage in Patients with Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD).

Int J Mol Sci. 2024-4-16

[7]
Breaking the barriers: the role of gut homeostasis in Metabolic-Associated Steatotic Liver Disease (MASLD).

Gut Microbes. 2024

[8]
The multifaceted roles of B lymphocytes in metabolic dysfunction-associated steatotic liver disease.

Front Immunol. 2024

[9]
The Lasting Effects of COVID-19 on the Progression of Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD).

Cureus. 2023-9-14

[10]
Role of the type 3 cytokines IL-17 and IL-22 in modulating metabolic dysfunction-associated steatotic liver disease.

Front Immunol. 2024

引用本文的文献

[1]
Differential Profiles of Gut Microbiota-Derived Metabolites of Bile Acids and Propionate as Potential Predictors of Depressive Disorder in Women with Morbid Obesity at High Risk of Metabolic Dysfunction-Associated Steatotic Liver Disease-A Pilot Study.

Curr Issues Mol Biol. 2025-5-12

[2]
Macronutrient Modulation in Metabolic Dysfunction-Associated Steatotic Liver Disease-the Molecular Role of Fatty Acids compared with Sugars in Human Metabolism and Disease Progression.

Adv Nutr. 2025-3

[3]
sp. for the Attenuation of Metabolic Dysfunction-Associated Steatotic Liver Disease in Mice.

Microorganisms. 2024-12-3

[4]
The Role of Microbiota-Related Co-Metabolites in MASLD Progression: A Narrative Review.

Curr Issues Mol Biol. 2024-6-25

本文引用的文献

[1]
The heated debate over NAFLD renaming: An ongoing saga.

Hepatol Forum. 2023-9-7

[2]
A multisociety Delphi consensus statement on new fatty liver disease nomenclature.

J Hepatol. 2023-12

[3]
Gut dysbiosis in nonalcoholic fatty liver disease: pathogenesis, diagnosis, and therapeutic implications.

Front Cell Infect Microbiol. 2022

[4]
Microbiome-derived ethanol in nonalcoholic fatty liver disease.

Nat Med. 2022-10

[5]
Corrigendum: The Microbiota and It's Correlation With Metabolites in the Gut of Mice With Nonalcoholic Fatty Liver Disease.

Front Cell Infect Microbiol. 2022-7-5

[6]
Occurrences and Functions of Ly6C and Ly6C Macrophages in Health and Disease.

Front Immunol. 2022

[7]
The Gut-Liver Axis in Nonalcoholic Fatty Liver Disease: Association of Intestinal Permeability with Disease Severity and Treatment Outcomes.

Int J Clin Pract. 2022

[8]
Risk assessment with gut microbiome and metabolite markers in NAFLD development.

Sci Transl Med. 2022-6-8

[9]
Longitudinal 16S rRNA Sequencing Reveals Relationships among Alterations of Gut Microbiota and Nonalcoholic Fatty Liver Disease Progression in Mice.

Microbiol Spectr. 2022-6-29

[10]
Gut microbial community differentially characterizes patients with nonalcoholic fatty liver disease.

J Gastroenterol Hepatol. 2022-9

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