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 |
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| Sprache: | Englisch |
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Springer Japan
01.01.2017
Springer Nature B.V |
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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. |
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| 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 – sequence: 2 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 – sequence: 3 givenname: Toshio surname: Kobayashi fullname: Kobayashi, Toshio organization: Miyagi University – sequence: 4 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 – sequence: 6 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 – sequence: 9 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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| Keywords | Gut microbiota Terminal restriction fragment length polymorphism (T-RFLP) Data mining analysis Coronary artery disease Decision tree |
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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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