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Exploring of gut microbiota features in dyslipidemia and chronic coronary syndrome patients undergoing coronary angiography

Chronic coronary syndrome (CCS) has a high mortality rate, and dyslipidemia is a major risk factor. Atherosclerosis, a cause of CCS, is influenced by gut microbiota dysbiosis and its metabolites. The objective of this study was to study the diversity and composition of gut microbiota and related cli...

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Bibliographic Details
Published in:Frontiers in microbiology 2024, Vol.15, p.1384146-1384146
Main Authors: Luangphiphat, Wongsakorn, Prombutara, Pinidphon, Muangsillapasart, Viroj, Sukitpunyaroj, Damrong, Eeckhout, Eric, Taweechotipatr, Malai
Format: Article
Language:English
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Summary:Chronic coronary syndrome (CCS) has a high mortality rate, and dyslipidemia is a major risk factor. Atherosclerosis, a cause of CCS, is influenced by gut microbiota dysbiosis and its metabolites. The objective of this study was to study the diversity and composition of gut microbiota and related clinical parameters among CCS patients undergoing coronary angiography and dyslipidemia patients in comparison to healthy volunteers in Thailand. CCS patients had more risk factors and higher inflammatory markers, high-sensitivity C-reactive protein (hs-CRP) than others. The alpha diversity was lower in dyslipidemia and CCS patients than in the healthy group. A significant difference in the composition of gut microbiota was observed among the three groups. The relative abundance of Proteobacteria, Fusobacteria, Enterobacteriaceae, and was significantly increased while , and were lower in CCS patients. In CCS patients, Lachnospiraceae, Peptostreptococcaceae, and were positively correlated with hs-CRP. In dyslipidemia patients, was strongly positively correlated with triglyceride (TG) level and negatively correlated with high-density lipoprotein cholesterol (HDL-C). The modification of gut microbiota was associated with changes in clinical parameters involved in the development of coronary artery disease (CAD) in CCS patients.
ISSN:1664-302X
1664-302X
DOI:10.3389/fmicb.2024.1384146