以微生物组为中心的治疗方法用于治疗代谢功能障碍相关性脂肪肝。

IF 14 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY
Huma Saeed, Luis Antonio Díaz, Antonio Gil-Gómez, Jeremy Burton, Jasmohan Bajaj, Manuel Romero-Gomez, Marco Arrese, Juan Pablo Arab, Mohammad Qasim Khan
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引用次数: 0

摘要

代谢功能障碍相关性脂肪性肝病(MASLD)是一个重大的全球性健康问题,由于肥胖和 2 型糖尿病(T2DM)等代谢风险因素的发病率不断上升,全球有 30% 以上的人患有该病。肝病的范围从孤立的脂肪变性到更严重的脂肪性肝炎、肝纤维化和肝硬化。最近的研究强调了肠道微生物群在 MASLD 发病机制中的作用,表明菌群失调会严重影响代谢健康和肝病的进展。本综述严格评估了目前在 MASLD 治疗中以微生物群为中心的疗法,包括益生菌、益生菌、合成益生菌、粪便微生物群移植(FMT)以及工程菌和噬菌体疗法等新兴疗法。我们将探讨这些干预措施影响 MASLD 的科学原理、临床证据和潜在机制。肠道-肝脏轴对 MASLD 至关重要,微生物组组成的显著变化与疾病进展有关。例如,特定的微生物特征和α多样性的减少与MASLD的严重程度有关。针对微生物组的治疗策略可以通过改善肠道通透性、减少产生内毒素的细菌和改变胆汁酸代谢来调节疾病的进展。尽管这些疗法前景广阔,但仍需进一步研究,以充分了解其机制并优化疗效。本综述综合了临床试验和实验研究的结果,全面概述了以微生物组为中心的疗法在控制 MASLD 方面的潜力。未来的研究应侧重于个性化策略,利用微生物组特征、血液代谢物和定制的饮食干预来提高这些疗法的疗效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Microbiome-Centered Therapies for the Management of Metabolic Dysfunction-Associated Steatotic Liver Disease.

Metabolic dysfunction-associated steatotic liver disease (MASLD) is a significant global health issue, affecting over 30% of the population worldwide due to the rising prevalence of metabolic risk factors such as obesity and type 2 diabetes mellitus (T2DM). This spectrum of liver disease ranges from isolated steatosis to more severe forms such as steatohepatitis, fibrosis, and cirrhosis. Recent studies highlight the role of gut microbiota in MASLD pathogenesis, showing that dysbiosis significantly impacts metabolic health and the progression of liver disease. This review critically evaluates current microbiome-centered therapies in MASLD management, including prebiotics, probiotics, synbiotics, fecal microbiota transplantation (FMT), and emerging therapies such as engineered bacteria and bacteriophage therapy. We explore the scientific rationale, clinical evidence, and potential mechanisms by which these interventions influence MASLD. The gut-liver axis is crucial in MASLD, with notable changes in microbiome composition linked to disease progression. For instance, specific microbial profiles and reduced alpha diversity are associated with MASLD severity. Therapeutic strategies targeting the microbiome could modulate disease progression by improving gut permeability, reducing endotoxin-producing bacteria, and altering bile acid metabolism. Although promising, these therapies require further research to fully understand their mechanisms and optimize their efficacy. This review integrates findings from clinical trials and experimental studies, providing a comprehensive overview of microbiome-centered therapies' potential in managing MASLD. Future research should focus on personalized strategies, utilizing microbiome features, blood metabolites, and customized dietary interventions to enhance the effectiveness of these therapies.

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来源期刊
Clinical and Molecular Hepatology
Clinical and Molecular Hepatology Medicine-Hepatology
CiteScore
15.60
自引率
9.00%
发文量
89
审稿时长
10 weeks
期刊介绍: Clinical and Molecular Hepatology is an internationally recognized, peer-reviewed, open-access journal published quarterly in English. Its mission is to disseminate cutting-edge knowledge, trends, and insights into hepatobiliary diseases, fostering an inclusive academic platform for robust debate and discussion among clinical practitioners, translational researchers, and basic scientists. With a multidisciplinary approach, the journal strives to enhance public health, particularly in the resource-limited Asia-Pacific region, which faces significant challenges such as high prevalence of B viral infection and hepatocellular carcinoma. Furthermore, Clinical and Molecular Hepatology prioritizes epidemiological studies of hepatobiliary diseases across diverse regions including East Asia, North Asia, Southeast Asia, Central Asia, South Asia, Southwest Asia, Pacific, Africa, Central Europe, Eastern Europe, Central America, and South America. The journal publishes a wide range of content, including original research papers, meta-analyses, letters to the editor, case reports, reviews, guidelines, editorials, and liver images and pathology, encompassing all facets of hepatology.
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