Characterization of gut microbiota profiles in coronary artery disease patients using data mining analysis of terminal restriction fragment length polymorphism: gut microbiota could be a diagnostic marker of coronary artery disease

The association between atherosclerosis and gut microbiota has been attracting increased attention. We previously demonstrated a possible link between gut microbiota and coronary artery disease. Our aim of this study was to clarify the gut microbiota profiles in coronary artery disease patients usin...

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Veröffentlicht in:Heart and vessels Jg. 32; H. 1; S. 39 - 46
Hauptverfasser: Emoto, Takuo, Yamashita, Tomoya, Kobayashi, Toshio, Sasaki, Naoto, Hirota, Yushi, Hayashi, Tomohiro, So, Anna, Kasahara, Kazuyuki, Yodoi, Keiko, Matsumoto, Takuya, Mizoguchi, Taiji, Ogawa, Wataru, Hirata, Ken-ichi
Format: Journal Article
Sprache:Englisch
Veröffentlicht: Tokyo Springer Japan 01.01.2017
Springer Nature B.V
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ISSN:0910-8327, 1615-2573
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Abstract The association between atherosclerosis and gut microbiota has been attracting increased attention. We previously demonstrated a possible link between gut microbiota and coronary artery disease. Our aim of this study was to clarify the gut microbiota profiles in coronary artery disease patients using data mining analysis of terminal restriction fragment length polymorphism (T-RFLP). This study included 39 coronary artery disease (CAD) patients and 30 age- and sex- matched no-CAD controls (Ctrls) with coronary risk factors. Bacterial DNA was extracted from their fecal samples and analyzed by T-RFLP and data mining analysis using the classification and regression algorithm. Five additional CAD patients were newly recruited to confirm the reliability of this analysis. Data mining analysis could divide the composition of gut microbiota into 2 characteristic nodes. The CAD group was classified into 4 CAD pattern nodes (35/39 = 90 %), while the Ctrl group was classified into 3 Ctrl pattern nodes (28/30 = 93 %). Five additional CAD samples were applied to the same dividing model, which could validate the accuracy to predict the risk of CAD by data mining analysis. We could demonstrate that operational taxonomic unit 853 (OTU853), OTU657, and OTU990 were determined important both by the data mining method and by the usual statistical comparison. We classified the gut microbiota profiles in coronary artery disease patients using data mining analysis of T-RFLP data and demonstrated the possibility that gut microbiota is a diagnostic marker of suffering from CAD.
AbstractList The association between atherosclerosis and gut microbiota has been attracting increased attention. We previously demonstrated a possible link between gut microbiota and coronary artery disease. Our aim of this study was to clarify the gut microbiota profiles in coronary artery disease patients using data mining analysis of terminal restriction fragment length polymorphism (T-RFLP). This study included 39 coronary artery disease (CAD) patients and 30 age- and sex- matched no-CAD controls (Ctrls) with coronary risk factors. Bacterial DNA was extracted from their fecal samples and analyzed by T-RFLP and data mining analysis using the classification and regression algorithm. Five additional CAD patients were newly recruited to confirm the reliability of this analysis. Data mining analysis could divide the composition of gut microbiota into 2 characteristic nodes. The CAD group was classified into 4 CAD pattern nodes (35/39 = 90 %), while the Ctrl group was classified into 3 Ctrl pattern nodes (28/30 = 93 %). Five additional CAD samples were applied to the same dividing model, which could validate the accuracy to predict the risk of CAD by data mining analysis. We could demonstrate that operational taxonomic unit 853 (OTU853), OTU657, and OTU990 were determined important both by the data mining method and by the usual statistical comparison. We classified the gut microbiota profiles in coronary artery disease patients using data mining analysis of T-RFLP data and demonstrated the possibility that gut microbiota is a diagnostic marker of suffering from CAD.
The association between atherosclerosis and gut microbiota has been attracting increased attention. We previously demonstrated a possible link between gut microbiota and coronary artery disease. Our aim of this study was to clarify the gut microbiota profiles in coronary artery disease patients using data mining analysis of terminal restriction fragment length polymorphism (T-RFLP). This study included 39 coronary artery disease (CAD) patients and 30 age- and sex- matched no-CAD controls (Ctrls) with coronary risk factors. Bacterial DNA was extracted from their fecal samples and analyzed by T-RFLP and data mining analysis using the classification and regression algorithm. Five additional CAD patients were newly recruited to confirm the reliability of this analysis. Data mining analysis could divide the composition of gut microbiota into 2 characteristic nodes. The CAD group was classified into 4 CAD pattern nodes (35/39 = 90 %), while the Ctrl group was classified into 3 Ctrl pattern nodes (28/30 = 93 %). Five additional CAD samples were applied to the same dividing model, which could validate the accuracy to predict the risk of CAD by data mining analysis. We could demonstrate that operational taxonomic unit 853 (OTU853), OTU657, and OTU990 were determined important both by the data mining method and by the usual statistical comparison. We classified the gut microbiota profiles in coronary artery disease patients using data mining analysis of T-RFLP data and demonstrated the possibility that gut microbiota is a diagnostic marker of suffering from CAD.
Author Kobayashi, Toshio
Yamashita, Tomoya
Kasahara, Kazuyuki
Mizoguchi, Taiji
Hayashi, Tomohiro
Hirata, Ken-ichi
Yodoi, Keiko
Matsumoto, Takuya
Emoto, Takuo
So, Anna
Hirota, Yushi
Ogawa, Wataru
Sasaki, Naoto
Author_xml – sequence: 1
  givenname: Takuo
  surname: Emoto
  fullname: Emoto, Takuo
  organization: Division of Cardiovascular Medicine, Department of Internal Medicine, Kobe University Graduate School of Medicine
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  givenname: Tomoya
  surname: Yamashita
  fullname: Yamashita, Tomoya
  email: tomoya@med.kobe-u.ac.jp
  organization: Division of Cardiovascular Medicine, Department of Internal Medicine, Kobe University Graduate School of Medicine
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  givenname: Toshio
  surname: Kobayashi
  fullname: Kobayashi, Toshio
  organization: Miyagi University
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  givenname: Naoto
  surname: Sasaki
  fullname: Sasaki, Naoto
  organization: Division of Cardiovascular Medicine, Department of Internal Medicine, Kobe University Graduate School of Medicine
– sequence: 5
  givenname: Yushi
  surname: Hirota
  fullname: Hirota, Yushi
  organization: Division of Diabetes and Endocrinology, Department of Internal Medicine, Kobe University Graduate School of Medicine
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  givenname: Tomohiro
  surname: Hayashi
  fullname: Hayashi, Tomohiro
  organization: Division of Cardiovascular Medicine, Department of Internal Medicine, Kobe University Graduate School of Medicine
– sequence: 7
  givenname: Anna
  surname: So
  fullname: So, Anna
  organization: Division of Diabetes and Endocrinology, Department of Internal Medicine, Kobe University Graduate School of Medicine
– sequence: 8
  givenname: Kazuyuki
  surname: Kasahara
  fullname: Kasahara, Kazuyuki
  organization: Division of Cardiovascular Medicine, Department of Internal Medicine, Kobe University Graduate School of Medicine
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  givenname: Keiko
  surname: Yodoi
  fullname: Yodoi, Keiko
  organization: Division of Cardiovascular Medicine, Department of Internal Medicine, Kobe University Graduate School of Medicine
– sequence: 10
  givenname: Takuya
  surname: Matsumoto
  fullname: Matsumoto, Takuya
  organization: Division of Cardiovascular Medicine, Department of Internal Medicine, Kobe University Graduate School of Medicine
– sequence: 11
  givenname: Taiji
  surname: Mizoguchi
  fullname: Mizoguchi, Taiji
  organization: Division of Cardiovascular Medicine, Department of Internal Medicine, Kobe University Graduate School of Medicine
– sequence: 12
  givenname: Wataru
  surname: Ogawa
  fullname: Ogawa, Wataru
  organization: Division of Diabetes and Endocrinology, Department of Internal Medicine, Kobe University Graduate School of Medicine
– sequence: 13
  givenname: Ken-ichi
  surname: Hirata
  fullname: Hirata, Ken-ichi
  organization: Division of Cardiovascular Medicine, Department of Internal Medicine, Kobe University Graduate School of Medicine
BackLink https://www.ncbi.nlm.nih.gov/pubmed/27125213$$D View this record in MEDLINE/PubMed
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ContentType Journal Article
Copyright Springer Japan 2016
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ISSN 0910-8327
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Issue 1
Keywords Gut microbiota
Terminal restriction fragment length polymorphism (T-RFLP)
Data mining analysis
Coronary artery disease
Decision tree
Language English
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Springer Nature B.V
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Snippet The association between atherosclerosis and gut microbiota has been attracting increased attention. We previously demonstrated a possible link between gut...
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StartPage 39
SubjectTerms Aged
Atherosclerosis
Bacteria
Biomarkers
Biomedical Engineering and Bioengineering
Cardiac Surgery
Cardiology
Cardiovascular disease
Case-Control Studies
Coronary Artery Disease - diagnosis
Coronary Artery Disease - microbiology
Data analysis
Data Mining
Decision trees
DNA, Bacterial - genetics
Feces - microbiology
Female
Gastrointestinal Microbiome
Humans
Japan
Male
Medicine
Medicine & Public Health
Middle Aged
Original Article
Polymorphism
Polymorphism, Restriction Fragment Length
Vascular Surgery
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Title Characterization of gut microbiota profiles in coronary artery disease patients using data mining analysis of terminal restriction fragment length polymorphism: gut microbiota could be a diagnostic marker of coronary artery disease
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