4.7 Article

Aggravated Gut Microbiota and Metabolomic Imbalances Are Associated with Hypertension Patients Comorbid with Atrial Fibrillation

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BIOMOLECULES
卷 12, 期 10, 页码 -

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MDPI
DOI: 10.3390/biom12101445

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atrial fibrillation; hypertension; metagenome; metabolome; saturated fatty acids; unsaturated fatty acids

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This study explored the altered gut microbiota community and metabolic patterns in hypertensive patients with atrial fibrillation (HTN-AF), compared to hypertensive patients without AF. The study found significant differences in microbial diversity and dominant species between the two groups, as well as changes in metabolite levels, particularly saturated and unsaturated fatty acids. These findings suggest that the dysbiosis of gut microbiota and imbalances in metabolites are associated with increased susceptibility to AF in hypertensive patients. This provides potential targets for AF prediction and prevention in hypertensive patients.
Disordered gut microbiota (GM) as the co-contributor of atrial fibrillation (AF) and hypertension (HTN) might be associated with AF risk in HTN. This study aimed to explore the altered GM community and metabolic patterns between 27 HTN patients with AF (HTN-AF) and 27 non-AF HTN patients through fecal metagenomic and serum metabolomic analysis. Compared to non-AF HTN patients, significant microbial alterations (p = 0.004), including increased microbial diversity (p < 0.05), shifted enterotype dominated by Prevotella to Bacteroides, and abundant disease-linked genera Ruminococcus, Streptococcus, Veillonella, Dorea, and Enterococcus, were observed in HTN-AF patients. A species-based random forest prediction model was associated with the risk of AF occurrence in HTN patients. Furthermore, GM metabolic profiles dramatically differed between HTN and HTN-AF patients, especially the imbalance of saturated and unsaturated fatty acids. In HTN-AF patients, circulating palmitic acid and arachidonic acid levels were significantly elevated, while the levels of tetracosahexaenoic acid, oleic acid, linoleic acid, and stearic acid were decreased (p < 0.001, VIP > 1), mediating 85.99% of gut microbial indirect effects on AF (p < 0.001). Thus, our findings preliminarily indicated that exacerbated dysbiosis of GM and relevant metabolites was associated with high AF susceptibility and might be a potential target for AF prediction and prevention in HTN.

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