Department of Chemistry and Biology "A. Zambelli", University of Salerno, Via Giovanni Paolo II 132, 84084 Fisciano, SA, Italy.
European Institute of Metabolomics (EIM) Foundation, Via G. Puccini, 3, 84081 Baronissi, SA, Italy.
Nutrients. 2024 Apr 1;16(7):1025. doi: 10.3390/nu16071025.
Portal hypertension (PH) is a complex clinical challenge with severe complications, including variceal bleeding, ascites, hepatic encephalopathy, and hepatorenal syndrome. The gut microbiota (GM) and its interconnectedness with human health have emerged as a captivating field of research. This review explores the intricate connections between the gut and the liver, aiming to elucidate how alterations in GM, intestinal barrier function, and gut-derived molecules impact the development and progression of PH. A systematic literature search, following PRISMA guidelines, identified 12 original articles that suggest a relationship between GM, the gut-liver axis, and PH. Mechanisms such as dysbiosis, bacterial translocation, altered microbial structure, and inflammation appear to orchestrate this relationship. One notable study highlights the pivotal role of the farnesoid X receptor axis in regulating the interplay between the gut and liver and proposes it as a promising therapeutic target. Fecal transplantation experiments further emphasize the pathogenic significance of the GM in modulating liver maladies, including PH. Recent advancements in metagenomics and metabolomics have expanded our understanding of the GM's role in human ailments. The review suggests that addressing the unmet need of identifying gut-liver axis-related metabolic and molecular pathways holds potential for elucidating pathogenesis and directing novel therapeutic interventions.
门静脉高压症 (PH) 是一种具有严重并发症的复杂临床挑战,包括静脉曲张出血、腹水、肝性脑病和肝肾综合征。肠道微生物群 (GM) 及其与人类健康的相互联系已成为一个引人入胜的研究领域。本综述探讨了肠道和肝脏之间的复杂联系,旨在阐明 GM 改变、肠道屏障功能和肠道来源分子如何影响 PH 的发生和发展。根据 PRISMA 指南进行系统文献检索,确定了 12 篇原始文章,这些文章表明 GM、肠道-肝脏轴和 PH 之间存在关系。例如,生态失调、细菌易位、微生物结构改变和炎症等机制似乎在协调这种关系。一项引人注目的研究强调了法尼醇 X 受体轴在调节肠道和肝脏相互作用中的关键作用,并提出它作为一个有前途的治疗靶点。粪便移植实验进一步强调了 GM 在调节肝脏疾病(包括 PH)中的致病意义。宏基因组学和代谢组学的最新进展扩展了我们对 GM 在人类疾病中的作用的理解。该综述表明,解决确定与肠道-肝脏轴相关的代谢和分子途径的未满足需求,有可能阐明发病机制并指导新的治疗干预。