Advances in the study of oral microbiota and metabolism associated fatty liver disease: a systematic review.

IF 4.6 2区 医学 Q2 IMMUNOLOGY Frontiers in Cellular and Infection Microbiology Pub Date : 2024-11-12 eCollection Date: 2024-01-01 DOI:10.3389/fcimb.2024.1491696
Mingming Huang, Xinbi Zhang, Rui Zhou, Yingzhe Song, Jing Zhang, Jian Wu
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Abstract

Objective: The oral microbiota is the second largest microbiota in the human body and has a significant impact on human health. Recent evidence suggests that dysbiosis of the oral microbiota may be associated with the development of metabolism-associated fatty liver disease (MAFLD). This review aimed to validate the relationship between oral microbial diversity and the development of MAFLD.

Methods: A systematic evaluation was performed based on PRISMA guidelines. Three independent reviewers searched for relevant literature in several databases, including PubMed/Medline, Web of Science, and Scopus, with a search date ranging from the establishment of the databases to June 2024.

Results: A total of 1278 publications were initially screened, including five cross-sectional studies, seven case-control studies, one cohort study, and one retrospective study. These studies included a total of 3335 patients with MAFLD, 254 patients with MASH, and 105 patients with liver cirrhosis. All 14 included studies concluded that there was a correlation or potential correlation between oral microbiota and MAFLD. Seven studies found that the composition of the oral microbiota in MAFLD patients differed from that of healthy controls, and specific oral bacteria may be associated with an increased incidence of MAFLD. At the phylum level, several studies found differences in the abundance of the phyla Firmicutes, Proteobacteria, and Clostridia compared to healthy controls. Additionally, a study on oral fungi found significant differences in the phyla Proteobacteria and in the genus Staphylococcus between patients with MAFLD and healthy controls. At the genus level, Porphyromonas was studied most frequently, with all 8 studies identifying infection with Porphyromonas as a significant risk factor for pathological progression in MAFLD. Furthermore, a dysbiosis in the ratio of Porphyromonas gingivalis./Porphyromonas anomalies may be an important marker of MAFLD progression.

Conclusion: There is an important association between the diversity of oral microbiota composition and MAFLD. This finding suggests the importance of oral health assessment and monitoring for the prevention or intervention of MAFLD.

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口腔微生物群与代谢相关脂肪肝研究进展:系统综述。
目的:口腔微生物群是人体内第二大微生物群,对人体健康有重大影响。最近的证据表明,口腔微生物菌群失调可能与代谢相关性脂肪肝(MAFLD)的发生有关。本综述旨在验证口腔微生物多样性与 MAFLD 发病之间的关系:方法:根据 PRISMA 指南进行了系统评估。三位独立审稿人在多个数据库中检索了相关文献,包括 PubMed/Medline、Web of Science 和 Scopus,检索日期从数据库建立之初到 2024 年 6 月:共初步筛选出 1278 篇文献,包括 5 项横断面研究、7 项病例对照研究、1 项队列研究和 1 项回顾性研究。这些研究共纳入了 3335 名 MAFLD 患者、254 名 MASH 患者和 105 名肝硬化患者。所纳入的 14 项研究均认为,口腔微生物群与 MAFLD 之间存在相关性或潜在相关性。七项研究发现,MAFLD 患者口腔微生物群的组成与健康对照组不同,特定的口腔细菌可能与 MAFLD 发病率的增加有关。在菌门层面,几项研究发现,与健康对照组相比,固缩菌门、变形菌门和梭状芽孢杆菌门的丰度存在差异。此外,一项关于口腔真菌的研究发现,在变形菌门和葡萄球菌属中,MAFLD 患者与健康对照组之间存在显著差异。在属的层面上,卟啉单胞菌被研究得最多,所有8项研究都认为感染卟啉单胞菌是MAFLD病理进展的一个重要风险因素。此外,牙龈卟啉单胞菌/异常卟啉单胞菌比例失调可能是 MAFLD 病变进展的重要标志:结论:口腔微生物群组成的多样性与 MAFLD 之间存在重要关联。这一发现表明,口腔健康评估和监测对于预防或干预 MAFLD 非常重要。
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来源期刊
CiteScore
7.90
自引率
7.00%
发文量
1817
审稿时长
14 weeks
期刊介绍: Frontiers in Cellular and Infection Microbiology is a leading specialty journal, publishing rigorously peer-reviewed research across all pathogenic microorganisms and their interaction with their hosts. Chief Editor Yousef Abu Kwaik, University of Louisville is supported by an outstanding Editorial Board of international experts. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. Frontiers in Cellular and Infection Microbiology includes research on bacteria, fungi, parasites, viruses, endosymbionts, prions and all microbial pathogens as well as the microbiota and its effect on health and disease in various hosts. The research approaches include molecular microbiology, cellular microbiology, gene regulation, proteomics, signal transduction, pathogenic evolution, genomics, structural biology, and virulence factors as well as model hosts. Areas of research to counteract infectious agents by the host include the host innate and adaptive immune responses as well as metabolic restrictions to various pathogenic microorganisms, vaccine design and development against various pathogenic microorganisms, and the mechanisms of antibiotic resistance and its countermeasures.
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