Cited by 315Gut microbiota and healthOral microbiology and periodontitis researchNutritional Studies and Diet

Analysis of Gut Microbiota in Coronary Artery Disease Patients: a Possible Link between Gut Microbiota and Coronary Artery Disease

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Emoto, Takuo, Yamashita, Tomoya, Sasaki, Naoto, Hirota, Yushi, Hayashi, Tomohiro, So, Anna, Kasahara, Kazuyuki, Yodoi, Keiko +4 more·2016·Journal of Atherosclerosis and Thrombosis

Abstract

AIM: Recent studies have suggested that metabolic disorders such as obesity and type 2 diabetes are associated with gut microbiota. The association between atherosclerosis and gut microbiota has also been attracting increased attention. Our aim was to specify a characteristic trend of gut microbiota in coronary artery disease (CAD). METHODS: This study included 39 CAD patients, 30 age- and sex-matched no-CAD controls (Ctrls) with coronary risk factors and 50 healthy volunteers (HVs) without coronary risk factors. Bacterial DNA was extracted from their fecal samples and analyzed by terminal restriction fragment length polymorphism. RESULTS: A characteristic change of gut microbiota was observed in CAD patients, where the order Lactobacillales was increased (CAD, Ctrl vs. HV; 13.6%±12.0%, 6.2%±7.7% vs. 4.1%±5.9%; p<0.001) and the phylum Bacteroidetes (Bacteroides+Prevotella) was decreased (CAD, Ctrl vs. HV;35.5%±11.6%, 43.9%±11.2% vs. 47.4%±11.5%; p<0.001). The CAD group was over-represented in enterotype "others" (III), compared with the Ctrl or HV group (p<0.001, chi-squared test), although we could not deny the possibility that some drugs affect the gut flora types. CONCLUSIONS: Although this study had some limitations, we demonstrated that the incidence of CAD was linked with an alteration of gut microbiota. A prospective study is desired to clarify a causal relationship between CAD and gut microbiota.

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  1. Wu GD, Chen J, Hoffmann C, Bittinger K, Chen YY, Keilbaugh SA, Bewtra M, Knights D, Walters WA, Knight R, Sinha R, Gilroy E, Gupta K, Baldassano R, Nessel L, Li H, Bushman FD and Lewis JD: Linking come! European heart journal, 2013;
  2. Nagashima K. Mochizuki J, Hisada T, Suzuki S, Shimo- mura S. Phylogenetic Analysis of 16S Ribosomal RNA Gene Sequences from Human Fecal Microbiota and lmproved Utility of Terminal Restriction Fragment Length Polymorphism Profiling. Bioscience Microflora 2006; 25: 99-107

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Authors
Emoto, T., Yamashita, T., Sasaki, N., Hirota, Y., Hayashi, T., So, A., Kasahara, K., Yodoi, K., Matsumoto, T., Mizoguchi, T., Ogawa, W., & Hirata, K.-I.
Affiliations
Kobe University (JP)
Venue
Journal of Atherosclerosis and Thrombosis
Published
2016
Volume
23
Issue
8
Pages
908-921
ISSN
  • 1340-3478 (ISSN-L)
  • 1880-3873
OpenAlex
W2293306613
Cited by
315
References
24
Citations by year
2026: 17 · 2025: 30 · 2024: 38 · 2023: 32 · 2022: 58 · 2021: 44 · 2020: 33 · 2019: 18 · 2018: 20 · 2017: 11 · 2016: 13
FWCI
10.74
Type
journal article
Language
en
Open access
Licence
cc-by-nc-sa
Locations
  • Journal of Atherosclerosis and Thrombosis (publishedVersion, cc-by-nc-sa)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
  • Kobe University Repository Kernel (Kobe University) (submittedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
  • Health Sciences › Dentistry › Periodontics › Oral microbiology and periodontitis research
  • Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Nutritional Studies and Diet
Keywords
gut microbiota, coronary artery disease, Lactobacillales, Bacteroidetes, enterotypes, atherosclerosis, fecal microbiota, obesity, type 2 diabetes, coronary risk factors
MeSH terms
Gastrointestinal Microbiome, Aged, Coronary Artery Disease, Diabetes Mellitus, Type 2, DNA, Bacterial, Feces, Female, Humans, Male, Middle Aged, Obesity, Polymorphism, Restriction Fragment Length, Risk Factors, Case-Control Studies, Bacteroidetes

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