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非酒精性脂肪性肝炎患者的自动酿酒综合征和内源性乙醇生成:来自慢性肝病的视角

Autobrewery Syndrome and Endogenous Ethanol Production in Patients with MASLD: A Perspective from Chronic Liver Disease.

作者信息

Andaloro Silvia, De Gaetano Valeria, Cardone Ferdinando, Ianiro Gianluca, Cerrito Lucia, Pallozzi Maria, Stella Leonardo, Gasbarrini Antonio, Ponziani Francesca Romana

机构信息

Department of Translational Medicine and Surgery, Catholic University, 00168 Rome, Italy.

Liver Unit, CEMAD Centro Malattie dell'Apparato Digerente, Medicina Interna e Gastroenterologia, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, 00168 Rome, Italy.

出版信息

Int J Mol Sci. 2025 Jul 30;26(15):7345. doi: 10.3390/ijms26157345.


DOI:10.3390/ijms26157345
PMID:40806476
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12347242/
Abstract

Autobrewery syndrome is a rare condition characterized by the endogenous fermentation of carbohydrates by gut microbiota, which exceeds the liver's detoxification capacity and leads to signs and symptoms of acute alcohol intoxication. This condition has significant clinical, social, and legal implications. Beyond the acute effects, the role of excessive endogenous ethanol production in the progression of chronic diseases-particularly liver disease-is still under investigation. In this review, we aim to describe the key clinical features of autobrewery syndrome, identify the main microbial pathogens involved, and explore the potential impact of endogenous ethanol production on the development and progression of chronic liver disease. Although robust data and standardized treatment protocols are currently lacking, we discuss the general principles of management and outline possible therapeutic strategies and future perspectives.

摘要

自酿综合征是一种罕见病症,其特征为肠道微生物群对碳水化合物进行内源性发酵,这种发酵超过了肝脏的解毒能力,进而导致急性酒精中毒的体征和症状。这种病症具有重大的临床、社会和法律意义。除了急性影响外,内源性乙醇过度产生在慢性疾病(尤其是肝脏疾病)进展中的作用仍在研究中。在本综述中,我们旨在描述自酿综合征的关键临床特征,确定主要涉及的微生物病原体,并探讨内源性乙醇产生对慢性肝病发展和进展的潜在影响。尽管目前缺乏有力的数据和标准化的治疗方案,但我们讨论了管理的一般原则,并概述了可能的治疗策略和未来前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6eb/12347242/b5d2d2063676/ijms-26-07345-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6eb/12347242/d1be405cdfd5/ijms-26-07345-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6eb/12347242/b5d2d2063676/ijms-26-07345-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6eb/12347242/d1be405cdfd5/ijms-26-07345-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6eb/12347242/b5d2d2063676/ijms-26-07345-g002.jpg

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本文引用的文献

[1]
Immunomodulatory effects of CCFM8661 + stachyose on cyclophosphamide-induced immunosuppression mice.

Front Immunol. 2025-1-27

[2]
The gut microbiota-brain connection: insights into major depressive disorder and bipolar disorder.

Front Psychiatry. 2024-11-5

[3]
Gut Mycobiome and Asthma.

J Fungi (Basel). 2024-3-1

[4]
Auto-Brewery Syndrome After COVID-19 Infection.

ACG Case Rep J. 2024-2-8

[5]
Dynamics of the Gut Mycobiome in Patients With Ulcerative Colitis.

Clin Gastroenterol Hepatol. 2024-4

[6]
Bacteriophage targeting microbiota alleviates non-alcoholic fatty liver disease induced by high alcohol-producing Klebsiella pneumoniae.

Nat Commun. 2023-6-3

[7]
The Influence of the Oral Microbiome on Oral Cancer: A Literature Review and a New Approach.

Biomolecules. 2023-5-11

[8]
Shifting microbiomes: pathobionts hiding in our guts.

EBioMedicine. 2023-6

[9]
Three Klebsiella species as potential pathobionts generating endogenous ethanol in a clinical cohort of patients with auto-brewery syndrome: a case control study.

EBioMedicine. 2023-5

[10]
Gut mycobiome dysbiosis and its impact on intestinal permeability in attention-deficit/hyperactivity disorder.

J Child Psychol Psychiatry. 2023-9

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