1. Non-Ischemic Heart Failure With Reduced Ejection Fraction Is Associated With Altered Intestinal Microbiota
- Author
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Hidetaka Kioka, Ryu Okumura, Shota Nakamura, Tetsuya Iida, Kei Nakamoto, Yasumasa Tsukamoto, Themistoklis Katsimichas, Hiroshi Miyawaki, Tomohito Ohtani, Misato Chimura, Kiyoshi Takeda, Taiki Sakaguchi, Kaoruko Sengoku, Konstantinos Theofilis, Shozo Konishi, Daisuke Motooka, and Yasushi Sakata
- Subjects
DNA, Bacterial ,0301 basic medicine ,Vitamin ,Firmicutes ,030204 cardiovascular system & hematology ,Gut flora ,Microbiology ,Veillonella ,03 medical and health sciences ,chemistry.chemical_compound ,0302 clinical medicine ,Microbial ecology ,RNA, Ribosomal, 16S ,medicine ,Humans ,Heart Failure ,biology ,Bacteroidetes ,Streptococcus ,Stroke Volume ,General Medicine ,Classification ,biology.organism_classification ,medicine.disease ,Gastrointestinal Microbiome ,030104 developmental biology ,chemistry ,Case-Control Studies ,Cardiology and Cardiovascular Medicine ,Dysbiosis ,Bacteria ,Drug metabolism - Abstract
Background Research suggests that heart failure with reduced ejection fraction (HFrEF) is a state of systemic inflammation that may be triggered by microbial products passing into the bloodstream through a compromised intestinal barrier. However, whether the intestinal microbiota exhibits dysbiosis in HFrEF patients is largely unknown.Methods and Results:Twenty eight non-ischemic HFrEF patients and 19 healthy controls were assessed by 16S rRNA analysis of bacterial DNA extracted from stool samples. After processing of sequencing data, bacteria were taxonomically classified, diversity indices were used to examine microbial ecology, and relative abundances of common core genera were compared between groups. Furthermore, we predicted gene carriage for bacterial metabolic pathways and inferred microbial interaction networks on multiple taxonomic levels.Bacterial communities of both groups were dominated by the Firmicutes and Bacteroidetes phyla. The most abundant genus in both groups wasBacteroides. Although α diversity did not differ between groups, ordination by β diversity metrics revealed a separation of the groups across components of variation.StreptococcusandVeillonellawere enriched in the common core microbiota of patients, whileSMB53was depleted. Gene families in amino acid, carbohydrate, vitamin, and xenobiotic metabolism showed significant differences between groups. Interaction networks revealed a higher degree of correlations between bacteria in patients. Conclusions Non-ischemic HFrEF patients exhibited multidimensional differences in intestinal microbial communities compared with healthy subjects.
- Published
- 2018
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