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Impact of microRNA expression in human atrial tissue in patients with atrial fibrillation undergoing cardiac surgery
Although microRNA (miRNA) regulates initiation and/or progression of atrial fibrillation (AF) in canine AF models, the underlying mechanism in humans remains unclear. We speculated that certain miRNAs in atrial tissue are related to AF, and evaluated the relationship of miRNA expression in human atr...
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Published in: | PloS one 2013-09, Vol.8 (9), p.e73397-e73397 |
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description | Although microRNA (miRNA) regulates initiation and/or progression of atrial fibrillation (AF) in canine AF models, the underlying mechanism in humans remains unclear. We speculated that certain miRNAs in atrial tissue are related to AF, and evaluated the relationship of miRNA expression in human atrial tissue in cardiac surgery patients.
Right atrial tissues from 29 patients undergoing cardiovascular surgery were divided into 3 groups [A: chronic AF or unsuccessful maze, n=6; B: successful maze, n=10; C: sinus rhythm (SR) n=13]. miRNA expression was determined using high density microarrays and with Reverse transcriptase-polymerase chain reaction (RT-PCR). Fibrosis was examined using Masson trichrome staining.
miRNA microarray analysis showed elevated miRNA-21, miRNA-23b, miRNA-199b, and miRNA-208b in AF as compared to SR groups. RT-PCR showed elevated miRNA-21 (1.9-fold) and miRNA-208b (4.2-fold) in AF as compared to the SR groups. miRNA-21 expression increased from Group C to A (A: 2.1-fold, B: 1.8-fold, C: 1.0-fold). Fibrosis increased from C to A (A: 43.0±12.9%, B: 21.3±6.1%, C: 11.9±3.1%). Percent fibrosis and miRNA-21 expression were correlated (r=0.508, p |
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Right atrial tissues from 29 patients undergoing cardiovascular surgery were divided into 3 groups [A: chronic AF or unsuccessful maze, n=6; B: successful maze, n=10; C: sinus rhythm (SR) n=13]. miRNA expression was determined using high density microarrays and with Reverse transcriptase-polymerase chain reaction (RT-PCR). Fibrosis was examined using Masson trichrome staining.
miRNA microarray analysis showed elevated miRNA-21, miRNA-23b, miRNA-199b, and miRNA-208b in AF as compared to SR groups. RT-PCR showed elevated miRNA-21 (1.9-fold) and miRNA-208b (4.2-fold) in AF as compared to the SR groups. miRNA-21 expression increased from Group C to A (A: 2.1-fold, B: 1.8-fold, C: 1.0-fold). Fibrosis increased from C to A (A: 43.0±12.9%, B: 21.3±6.1%, C: 11.9±3.1%). Percent fibrosis and miRNA-21 expression were correlated (r=0.508, p<0.05). The plasma levels of miRNA-21 in AF patients was significantly decreased as compared to the healthy volunteers (p<0.05).
The expression of miRNA-21 in human atrial tissue was found to be related to atrial fibrosis and might affect AF occurrence, indicating its usefulness as a biomarker for cardiac surgery management.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0073397</identifier><identifier>PMID: 24069193</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Aged ; Atrial fibrillation ; Atrial Fibrillation - genetics ; Atrial Fibrillation - metabolism ; Biomarkers ; Cardiac arrhythmia ; Cardiac Surgical Procedures ; Cardiovascular disease ; Care and treatment ; Coronary vessels ; DNA microarrays ; DNA polymerases ; Electrocardiography ; Fibrillation ; Fibrosis ; Heart ; Heart Atria - metabolism ; Heart diseases ; Heart failure ; Heart surgery ; Humans ; Medicine ; MicroRNA ; MicroRNAs ; MicroRNAs - genetics ; Middle Aged ; miRNA ; Patients ; Plasma levels ; Polymerase chain reaction ; Reverse Transcriptase Polymerase Chain Reaction ; Ribonucleic acid ; RNA ; RNA-directed DNA polymerase ; Sinus ; Studies ; Surgery ; Tissues ; University graduates</subject><ispartof>PloS one, 2013-09, Vol.8 (9), p.e73397-e73397</ispartof><rights>COPYRIGHT 2013 Public Library of Science</rights><rights>2013 Nishi et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2013 Nishi et al 2013 Nishi et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c775t-1f94cefc25ce3e88e2641762930963e10f73ccd3227c23954c3d8d93aac3e1da3</citedby><cites>FETCH-LOGICAL-c775t-1f94cefc25ce3e88e2641762930963e10f73ccd3227c23954c3d8d93aac3e1da3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1434401609/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1434401609?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24069193$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Hosoda, Toru</contributor><creatorcontrib>Nishi, Hiroyuki</creatorcontrib><creatorcontrib>Sakaguchi, Taichi</creatorcontrib><creatorcontrib>Miyagawa, Shigeru</creatorcontrib><creatorcontrib>Yoshikawa, Yasushi</creatorcontrib><creatorcontrib>Fukushima, Satsuki</creatorcontrib><creatorcontrib>Saito, Shunsuke</creatorcontrib><creatorcontrib>Ueno, Takayoshi</creatorcontrib><creatorcontrib>Kuratani, Toru</creatorcontrib><creatorcontrib>Sawa, Yoshiki</creatorcontrib><title>Impact of microRNA expression in human atrial tissue in patients with atrial fibrillation undergoing cardiac surgery</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Although microRNA (miRNA) regulates initiation and/or progression of atrial fibrillation (AF) in canine AF models, the underlying mechanism in humans remains unclear. We speculated that certain miRNAs in atrial tissue are related to AF, and evaluated the relationship of miRNA expression in human atrial tissue in cardiac surgery patients.
Right atrial tissues from 29 patients undergoing cardiovascular surgery were divided into 3 groups [A: chronic AF or unsuccessful maze, n=6; B: successful maze, n=10; C: sinus rhythm (SR) n=13]. miRNA expression was determined using high density microarrays and with Reverse transcriptase-polymerase chain reaction (RT-PCR). Fibrosis was examined using Masson trichrome staining.
miRNA microarray analysis showed elevated miRNA-21, miRNA-23b, miRNA-199b, and miRNA-208b in AF as compared to SR groups. RT-PCR showed elevated miRNA-21 (1.9-fold) and miRNA-208b (4.2-fold) in AF as compared to the SR groups. miRNA-21 expression increased from Group C to A (A: 2.1-fold, B: 1.8-fold, C: 1.0-fold). Fibrosis increased from C to A (A: 43.0±12.9%, B: 21.3±6.1%, C: 11.9±3.1%). Percent fibrosis and miRNA-21 expression were correlated (r=0.508, p<0.05). The plasma levels of miRNA-21 in AF patients was significantly decreased as compared to the healthy volunteers (p<0.05).
The expression of miRNA-21 in human atrial tissue was found to be related to atrial fibrosis and might affect AF occurrence, indicating its usefulness as a biomarker for cardiac surgery management.</description><subject>Aged</subject><subject>Atrial fibrillation</subject><subject>Atrial Fibrillation - genetics</subject><subject>Atrial Fibrillation - metabolism</subject><subject>Biomarkers</subject><subject>Cardiac arrhythmia</subject><subject>Cardiac Surgical Procedures</subject><subject>Cardiovascular disease</subject><subject>Care and treatment</subject><subject>Coronary vessels</subject><subject>DNA microarrays</subject><subject>DNA polymerases</subject><subject>Electrocardiography</subject><subject>Fibrillation</subject><subject>Fibrosis</subject><subject>Heart</subject><subject>Heart Atria - metabolism</subject><subject>Heart diseases</subject><subject>Heart failure</subject><subject>Heart surgery</subject><subject>Humans</subject><subject>Medicine</subject><subject>MicroRNA</subject><subject>MicroRNAs</subject><subject>MicroRNAs - genetics</subject><subject>Middle Aged</subject><subject>miRNA</subject><subject>Patients</subject><subject>Plasma levels</subject><subject>Polymerase chain reaction</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>Ribonucleic acid</subject><subject>RNA</subject><subject>RNA-directed DNA polymerase</subject><subject>Sinus</subject><subject>Studies</subject><subject>Surgery</subject><subject>Tissues</subject><subject>University graduates</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqNk9tu1DAQhiMEomXhDRBEQkJwsYtPieMbpFXFYaWKSuVwaznOJOsqiVPbgfbt8Xaz1Qb1Avki1sz3j-PfM0nyEqMVphx_uLKj61W7GmwPK4Q4pYI_Sk6xoGSZE0QfH-1PkmfeXyGU0SLPnyYnhKFcxOxpEjbdoHRIbZ12Rjt7-W2dws3gwHtj-9T06XbsVJ-q4Ixq02C8H2EXHlQw0Aef_jFhe0jXpnSmbWMqase-AtdY0zepVq4ySqd-dA242-fJk1q1Hl5M30Xy8_OnH2dfl-cXXzZn6_Ol5jwLS1wLpqHWJNNAoSiA5AzznAiKRE4Bo5pTrStKCNeEioxpWhWVoErpmK0UXSSv93WH1no5GeYlZpQxhHMkIrHZE5VVV3JwplPuVlpl5F3AukYqF4xuQVJc07LKGGOlZgTKEnOiUM04CAJcVLHWx-m0seyg0tEdp9pZ0XmmN1vZ2N-Sck5QfKVF8m4q4Oz1CD7IzngN0c8e7Hj33zwrUCZIRN_8gz58u4lqVLyA6Wsbz9W7onLNeEERyjMcqdUDVFwVxJaI3VWbGJ8J3s8EkQlwExo1ei833y__n734NWffHrFbUG3YetuOu27yc5Dtwdiw3juo703GSO6G4-CG3A2HnIYjyl4dP9C96DAN9C-LhwsQ</recordid><startdate>20130912</startdate><enddate>20130912</enddate><creator>Nishi, Hiroyuki</creator><creator>Sakaguchi, Taichi</creator><creator>Miyagawa, Shigeru</creator><creator>Yoshikawa, Yasushi</creator><creator>Fukushima, Satsuki</creator><creator>Saito, Shunsuke</creator><creator>Ueno, Takayoshi</creator><creator>Kuratani, Toru</creator><creator>Sawa, Yoshiki</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</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>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20130912</creationdate><title>Impact of microRNA expression in human atrial tissue in patients with atrial fibrillation undergoing cardiac surgery</title><author>Nishi, Hiroyuki ; Sakaguchi, Taichi ; Miyagawa, Shigeru ; Yoshikawa, Yasushi ; Fukushima, Satsuki ; Saito, Shunsuke ; Ueno, Takayoshi ; Kuratani, Toru ; Sawa, Yoshiki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c775t-1f94cefc25ce3e88e2641762930963e10f73ccd3227c23954c3d8d93aac3e1da3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Aged</topic><topic>Atrial fibrillation</topic><topic>Atrial Fibrillation - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nishi, Hiroyuki</au><au>Sakaguchi, Taichi</au><au>Miyagawa, Shigeru</au><au>Yoshikawa, Yasushi</au><au>Fukushima, Satsuki</au><au>Saito, Shunsuke</au><au>Ueno, Takayoshi</au><au>Kuratani, Toru</au><au>Sawa, Yoshiki</au><au>Hosoda, Toru</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Impact of microRNA expression in human atrial tissue in patients with atrial fibrillation undergoing cardiac surgery</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2013-09-12</date><risdate>2013</risdate><volume>8</volume><issue>9</issue><spage>e73397</spage><epage>e73397</epage><pages>e73397-e73397</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Although microRNA (miRNA) regulates initiation and/or progression of atrial fibrillation (AF) in canine AF models, the underlying mechanism in humans remains unclear. We speculated that certain miRNAs in atrial tissue are related to AF, and evaluated the relationship of miRNA expression in human atrial tissue in cardiac surgery patients.
Right atrial tissues from 29 patients undergoing cardiovascular surgery were divided into 3 groups [A: chronic AF or unsuccessful maze, n=6; B: successful maze, n=10; C: sinus rhythm (SR) n=13]. miRNA expression was determined using high density microarrays and with Reverse transcriptase-polymerase chain reaction (RT-PCR). Fibrosis was examined using Masson trichrome staining.
miRNA microarray analysis showed elevated miRNA-21, miRNA-23b, miRNA-199b, and miRNA-208b in AF as compared to SR groups. RT-PCR showed elevated miRNA-21 (1.9-fold) and miRNA-208b (4.2-fold) in AF as compared to the SR groups. miRNA-21 expression increased from Group C to A (A: 2.1-fold, B: 1.8-fold, C: 1.0-fold). Fibrosis increased from C to A (A: 43.0±12.9%, B: 21.3±6.1%, C: 11.9±3.1%). Percent fibrosis and miRNA-21 expression were correlated (r=0.508, p<0.05). The plasma levels of miRNA-21 in AF patients was significantly decreased as compared to the healthy volunteers (p<0.05).
The expression of miRNA-21 in human atrial tissue was found to be related to atrial fibrosis and might affect AF occurrence, indicating its usefulness as a biomarker for cardiac surgery management.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>24069193</pmid><doi>10.1371/journal.pone.0073397</doi><tpages>e73397</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aged Atrial fibrillation Atrial Fibrillation - genetics Atrial Fibrillation - metabolism Biomarkers Cardiac arrhythmia Cardiac Surgical Procedures Cardiovascular disease Care and treatment Coronary vessels DNA microarrays DNA polymerases Electrocardiography Fibrillation Fibrosis Heart Heart Atria - metabolism Heart diseases Heart failure Heart surgery Humans Medicine MicroRNA MicroRNAs MicroRNAs - genetics Middle Aged miRNA Patients Plasma levels Polymerase chain reaction Reverse Transcriptase Polymerase Chain Reaction Ribonucleic acid RNA RNA-directed DNA polymerase Sinus Studies Surgery Tissues University graduates |
title | Impact of microRNA expression in human atrial tissue in patients with atrial fibrillation undergoing cardiac surgery |
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