Key result
Bloodstream microbiota dysbiosis is linked to cardiometabolic disease, characterized by high Proteobacteria and low Bacteroides.
Why the study?
Dysbiosis of circulating bacteria is considered a key regulator of chronic inflammation implicated in cardio-metabolic diseases, but its role requires further clarification.
Is circulating bacterial dysbiosis associated with cardio-metabolic diseases in humans?
Meta-Analysis (n=11,132)
Is circulating bacterial dysbiosis associated with cardio-metabolic diseases in humans?
Circulating bacterial dysbiosis, specifically involving Proteobacteria, Firmicutes, and Bacteroidetes, is associated with cardio-metabolic diseases and may serve as a future biomarker or therapeutic target.
Dysbiosis of Proteobacteria, Firmicutes, and Bacteroidetes links to CMDs; leaves open causal role and therapeutic targeting.
AIMS: Scientists have recently discovered a link between the circulating microbiome and homeostasis, as well as the pathogenesis of a number of metabolic diseases. It has been demonstrated that low-grade chronic inflammation is one of the primary mechanisms that has long been implicated in the risk of cardio-metabolic disease (CMDs) and its progression. Currently, the dysbiosis of circulating bacteria is considered as a key regulator for chronic inflammation in CMDs, which is why we have conducted this systemic review focused on circulating bacterial dysbiosis. METHODS: A systemic review of clinical and research-based studies was conducted via PubMed, Scopus, Medline, and Web of Science. Literature was considered for risk of bias and patterns of intervention effects. A randomized effect model was used to evaluate the dysbiosis of circulating microbiota and clinical outcomes. We conducted a meta-analysis considering the circulating bacteria in both healthy people and people with cardio-metabolic disorders, in reports published mainly from 2008 to 2022, according to the PRISMA guidelines. RESULTS: We searched 627 studies and, after completing the risk of bias and selection, 31 studies comprising of 11,132 human samples were considered. This meta-analysis found that dysbiosis of phyla Proteobacteria, Firmicutes, and Bacteroidetes was associated with metabolic diseases. CONCLUSIONS: In most instances, metabolic diseases are linked to higher diversity and elevated bacterial DNA levels. Bacteroides abundance was higher in healthy people than with metabolic disorders. However, more rigorous studies are required to determine the role of bacterial dysbiosis in cardio-metabolic diseases. Understanding the relationship between dysbiosis and cardio-metabolic diseases, we can use the bacteria as therapeutics for the reversal of dysbiosis and targets for therapeutics use in cardio-metabolic diseases. In the future, circulating bacterial signatures can be used as biomarkers for the early detection of metabolic diseases.
No takes yet. Share an insight, caveat, or question.
Goraya et al. (2023) conducted a meta-analysis in Cardio-metabolic diseases (n=11,132). Blood stream microbiota dysbiosis vs. Healthy individuals (normal blood microbiota) was evaluated on Association of circulating bacterial dysbiosis with cardio-metabolic diseases. Blood stream microbiota dysbiosis, characterized by increased Proteobacteria and decreased Bacteroides abundance, is associated with cardio-metabolic diseases.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: