Analysis of Gut Microbiota in Coronary Artery Disease Patients: a Possible Link between Gut Microbiota and Coronary Artery Disease
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...
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Veröffentlicht in: | Journal of Atherosclerosis and Thrombosis 2016/08/01, Vol.23(8), pp.908-921 |
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creator | Emoto, Takuo Yamashita, Tomoya Sasaki, Naoto Hirota, Yushi Hayashi, Tomohiro So, Anna Kasahara, Kazuyuki Yodoi, Keiko Matsumoto, Takuya Mizoguchi, Taiji Ogawa, Wataru Hirata, Ken-ichi |
description | 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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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.</description><identifier>ISSN: 1340-3478</identifier><identifier>EISSN: 1880-3873</identifier><identifier>DOI: 10.5551/jat.32672</identifier><identifier>PMID: 26947598</identifier><language>eng</language><publisher>Japan: Japan Atherosclerosis Society</publisher><subject>Aged ; Bacteroidetes ; Bacteroidetes - pathogenicity ; Case-Control Studies ; Coronary artery disease ; Coronary Artery Disease - microbiology ; Coronary Artery Disease - physiopathology ; Diabetes Mellitus, Type 2 - complications ; DNA, Bacterial - genetics ; Feces - microbiology ; Female ; Gastrointestinal Microbiome - physiology ; Gut microbiota ; Humans ; Lactobacillales ; Male ; Middle Aged ; Obesity - complications ; Original ; Polymorphism, Restriction Fragment Length ; Risk Factors</subject><ispartof>Journal of Atherosclerosis and Thrombosis, 2016/08/01, Vol.23(8), pp.908-921</ispartof><rights>2016 This article is distributed under the terms of the latest version of CC BY-NC-SA defined by the Creative Commons Attribution License.</rights><rights>2016 Japan Atherosclerosis Society 2016</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c726t-142772d40466d40228a176ed72e5e6f0fff18ffbfe6380142049e097505445e53</citedby><cites>FETCH-LOGICAL-c726t-142772d40466d40228a176ed72e5e6f0fff18ffbfe6380142049e097505445e53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7399299/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7399299/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,1877,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26947598$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Emoto, Takuo</creatorcontrib><creatorcontrib>Yamashita, Tomoya</creatorcontrib><creatorcontrib>Sasaki, Naoto</creatorcontrib><creatorcontrib>Hirota, Yushi</creatorcontrib><creatorcontrib>Hayashi, Tomohiro</creatorcontrib><creatorcontrib>So, Anna</creatorcontrib><creatorcontrib>Kasahara, Kazuyuki</creatorcontrib><creatorcontrib>Yodoi, Keiko</creatorcontrib><creatorcontrib>Matsumoto, Takuya</creatorcontrib><creatorcontrib>Mizoguchi, Taiji</creatorcontrib><creatorcontrib>Ogawa, Wataru</creatorcontrib><creatorcontrib>Hirata, Ken-ichi</creatorcontrib><creatorcontrib>Division of Diabetes and Endocrinology</creatorcontrib><creatorcontrib>Division of Cardiovascular Medicine</creatorcontrib><creatorcontrib>Department of Internal Medicine</creatorcontrib><creatorcontrib>Kobe University Graduate School of Medicine</creatorcontrib><title>Analysis of Gut Microbiota in Coronary Artery Disease Patients: a Possible Link between Gut Microbiota and Coronary Artery Disease</title><title>Journal of Atherosclerosis and Thrombosis</title><addtitle>JAT</addtitle><description>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.</description><subject>Aged</subject><subject>Bacteroidetes</subject><subject>Bacteroidetes - pathogenicity</subject><subject>Case-Control Studies</subject><subject>Coronary artery disease</subject><subject>Coronary Artery Disease - microbiology</subject><subject>Coronary Artery Disease - physiopathology</subject><subject>Diabetes Mellitus, Type 2 - complications</subject><subject>DNA, Bacterial - genetics</subject><subject>Feces - microbiology</subject><subject>Female</subject><subject>Gastrointestinal Microbiome - physiology</subject><subject>Gut microbiota</subject><subject>Humans</subject><subject>Lactobacillales</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Obesity - complications</subject><subject>Original</subject><subject>Polymorphism, Restriction Fragment Length</subject><subject>Risk Factors</subject><issn>1340-3478</issn><issn>1880-3873</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kcuOEzEQRVsIxDxgwQ8gL2GRwc-2zQIUZSAgBTELWFvu7vKMQ8cebDeQLV-OkwwRILGpKqmObl3VbZonBF8IIciLtS0XjLaS3mtOiVJ4xpRk9-vMeJ25VCfNWc5rjBkTgj5sTmiruRRanTY_58GO2-wzig4tp4I--D7FzsdikQ9oEVMMNm3RPBWo7dJnsBnQlS0eQskvkUVXMWffjYBWPnxBHZTvAOFfLRuG_4k9ah44O2Z4fNfPm89v33xavJutPi7fL-arWS9pW2aEUynpwDFv21opVZbIFgZJQUDrsHOOKOc6By1TuNKYa8BaCiw4FyDYefPqoHs7dRsY-uo_2dHcJr-ppky03vy9Cf7GXMdvRjKtqdZV4NmdQIpfJ8jFbHzuYRxtgDhlQxRWTBGKaUWfH9D6gJwTuOMZgs0uM1MzM_vMKvv0T19H8ndIFVgegLr1vR1jGH0As45TquFlAz_kEDdbaygmrcH1PFa1CYP1btCUUMWw0KwqvT4orXOx13A8ZVPx_Qh7U5QZtSt7c8dNf2OTgcB-AfOBwJ0</recordid><startdate>20160101</startdate><enddate>20160101</enddate><creator>Emoto, Takuo</creator><creator>Yamashita, Tomoya</creator><creator>Sasaki, Naoto</creator><creator>Hirota, Yushi</creator><creator>Hayashi, Tomohiro</creator><creator>So, Anna</creator><creator>Kasahara, Kazuyuki</creator><creator>Yodoi, Keiko</creator><creator>Matsumoto, Takuya</creator><creator>Mizoguchi, Taiji</creator><creator>Ogawa, Wataru</creator><creator>Hirata, Ken-ichi</creator><general>Japan Atherosclerosis Society</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20160101</creationdate><title>Analysis of Gut Microbiota in Coronary Artery Disease Patients: a Possible Link between Gut Microbiota and Coronary Artery Disease</title><author>Emoto, Takuo ; Yamashita, Tomoya ; Sasaki, Naoto ; Hirota, Yushi ; Hayashi, Tomohiro ; So, Anna ; Kasahara, Kazuyuki ; Yodoi, Keiko ; Matsumoto, Takuya ; Mizoguchi, Taiji ; Ogawa, Wataru ; Hirata, Ken-ichi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c726t-142772d40466d40228a176ed72e5e6f0fff18ffbfe6380142049e097505445e53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Aged</topic><topic>Bacteroidetes</topic><topic>Bacteroidetes - pathogenicity</topic><topic>Case-Control Studies</topic><topic>Coronary artery disease</topic><topic>Coronary Artery Disease - microbiology</topic><topic>Coronary Artery Disease - physiopathology</topic><topic>Diabetes Mellitus, Type 2 - complications</topic><topic>DNA, Bacterial - genetics</topic><topic>Feces - microbiology</topic><topic>Female</topic><topic>Gastrointestinal Microbiome - physiology</topic><topic>Gut microbiota</topic><topic>Humans</topic><topic>Lactobacillales</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Obesity - complications</topic><topic>Original</topic><topic>Polymorphism, Restriction Fragment Length</topic><topic>Risk Factors</topic><toplevel>online_resources</toplevel><creatorcontrib>Emoto, Takuo</creatorcontrib><creatorcontrib>Yamashita, Tomoya</creatorcontrib><creatorcontrib>Sasaki, Naoto</creatorcontrib><creatorcontrib>Hirota, Yushi</creatorcontrib><creatorcontrib>Hayashi, Tomohiro</creatorcontrib><creatorcontrib>So, Anna</creatorcontrib><creatorcontrib>Kasahara, Kazuyuki</creatorcontrib><creatorcontrib>Yodoi, Keiko</creatorcontrib><creatorcontrib>Matsumoto, Takuya</creatorcontrib><creatorcontrib>Mizoguchi, Taiji</creatorcontrib><creatorcontrib>Ogawa, Wataru</creatorcontrib><creatorcontrib>Hirata, Ken-ichi</creatorcontrib><creatorcontrib>Division of Diabetes and Endocrinology</creatorcontrib><creatorcontrib>Division of Cardiovascular Medicine</creatorcontrib><creatorcontrib>Department of Internal Medicine</creatorcontrib><creatorcontrib>Kobe University Graduate School of Medicine</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of Atherosclerosis and Thrombosis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Emoto, Takuo</au><au>Yamashita, Tomoya</au><au>Sasaki, Naoto</au><au>Hirota, Yushi</au><au>Hayashi, Tomohiro</au><au>So, Anna</au><au>Kasahara, Kazuyuki</au><au>Yodoi, Keiko</au><au>Matsumoto, Takuya</au><au>Mizoguchi, Taiji</au><au>Ogawa, Wataru</au><au>Hirata, Ken-ichi</au><aucorp>Division of Diabetes and Endocrinology</aucorp><aucorp>Division of Cardiovascular Medicine</aucorp><aucorp>Department of Internal Medicine</aucorp><aucorp>Kobe University Graduate School of Medicine</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Analysis of Gut Microbiota in Coronary Artery Disease Patients: a Possible Link between Gut Microbiota and Coronary Artery Disease</atitle><jtitle>Journal of Atherosclerosis and Thrombosis</jtitle><addtitle>JAT</addtitle><date>2016-01-01</date><risdate>2016</risdate><volume>23</volume><issue>8</issue><spage>908</spage><epage>921</epage><pages>908-921</pages><issn>1340-3478</issn><eissn>1880-3873</eissn><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.</abstract><cop>Japan</cop><pub>Japan Atherosclerosis Society</pub><pmid>26947598</pmid><doi>10.5551/jat.32672</doi><tpages>14</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aged Bacteroidetes Bacteroidetes - pathogenicity Case-Control Studies Coronary artery disease Coronary Artery Disease - microbiology Coronary Artery Disease - physiopathology Diabetes Mellitus, Type 2 - complications DNA, Bacterial - genetics Feces - microbiology Female Gastrointestinal Microbiome - physiology Gut microbiota Humans Lactobacillales Male Middle Aged Obesity - complications Original Polymorphism, Restriction Fragment Length Risk Factors |
title | Analysis of Gut Microbiota in Coronary Artery Disease Patients: a Possible Link between Gut Microbiota and Coronary Artery Disease |
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