Association of circulating miR-20a, miR-27a, and miR-126 with non-alcoholic fatty liver disease in general population
Non-alcoholic fatty liver disease (NAFLD) is closely associated with obesity, metabolic syndrome, and type II diabetes mellitus. Recently, circulating microRNAs (miRNAs) have been proposed as useful disease biomarkers. We examined whether circulating miRNAs, such as miR-20a, miR-27a, and miR-126, we...
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creator | Ando, Yoshitaka Yamazaki, Mirai Yamada, Hiroya Munetsuna, Eiji Fujii, Ryosuke Mizuno, Genki Ichino, Naohiro Osakabe, Keisuke Sugimoto, Keiko Ishikawa, Hiroaki Ohashi, Koji Teradaira, Ryoji Ohta, Yoshiji Hamajima, Nobuyuki Hashimoto, Shuji Suzuki, Koji |
description | Non-alcoholic fatty liver disease (NAFLD) is closely associated with obesity, metabolic syndrome, and type II diabetes mellitus. Recently, circulating microRNAs (miRNAs) have been proposed as useful disease biomarkers. We examined whether circulating miRNAs, such as miR-20a, miR-27a, and miR-126, were useful biomarkers for NAFLD. We conducted a cross-sectional analysis of 527 subjects aged 39 years or older who had undergone a health examination in the Yakumo Study. Of the residents, 92 were diagnosed with NAFLD using a registered medical sonographer. Serum miR-20a, miR-27a and miR-126 levels were measured by quantitative real-time PCR. We then calculated the odds ratios for serum miRNA level changes according to the severity of NAFLD using normal liver status as the reference group. Serum levels of miR-20a and 27a, but not miR-126, were significantly lower in NAFLD subjects than normal subjects. Serum miR-20a and miR-27a levels were significantly lower in both male and female severe NAFLD subjects. Logistic regression analysis showed a significant relationship between low circulating miR-20a and 27a levels and severe NAFLD. Down-regulated circulating miR-20a and 27a levels were significantly associated with severe NAFLD in the general population. Circulating miR-20a and miR-27a may be useful biomarkers for severe NAFLD. |
doi_str_mv | 10.1038/s41598-019-55076-z |
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Recently, circulating microRNAs (miRNAs) have been proposed as useful disease biomarkers. We examined whether circulating miRNAs, such as miR-20a, miR-27a, and miR-126, were useful biomarkers for NAFLD. We conducted a cross-sectional analysis of 527 subjects aged 39 years or older who had undergone a health examination in the Yakumo Study. Of the residents, 92 were diagnosed with NAFLD using a registered medical sonographer. Serum miR-20a, miR-27a and miR-126 levels were measured by quantitative real-time PCR. We then calculated the odds ratios for serum miRNA level changes according to the severity of NAFLD using normal liver status as the reference group. Serum levels of miR-20a and 27a, but not miR-126, were significantly lower in NAFLD subjects than normal subjects. Serum miR-20a and miR-27a levels were significantly lower in both male and female severe NAFLD subjects. Logistic regression analysis showed a significant relationship between low circulating miR-20a and 27a levels and severe NAFLD. Down-regulated circulating miR-20a and 27a levels were significantly associated with severe NAFLD in the general population. Circulating miR-20a and miR-27a may be useful biomarkers for severe NAFLD.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/s41598-019-55076-z</identifier><identifier>PMID: 31827150</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>45 ; 692/308/174 ; 692/53 ; 692/699/1503/1607/2750 ; Adult ; Aged ; Biomarkers ; Biomarkers - blood ; Circulating MicroRNA - blood ; Cross-Sectional Studies ; Fatty liver ; Female ; Humanities and Social Sciences ; Humans ; Japan ; Liver diseases ; Male ; Metabolic disorders ; MicroRNAs ; MicroRNAs - blood ; Middle Aged ; multidisciplinary ; Non-alcoholic Fatty Liver Disease - blood ; Real-Time Polymerase Chain Reaction ; Regression analysis ; Science ; Science (multidisciplinary)</subject><ispartof>Scientific reports, 2019-12, Vol.9 (1), p.18856-8, Article 18856</ispartof><rights>The Author(s) 2019</rights><rights>2019. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c474t-f5e8ebb84462d2406ac47d0d69dc47791af0db0b656ccb7229ec7822702a1ffd3</citedby><cites>FETCH-LOGICAL-c474t-f5e8ebb84462d2406ac47d0d69dc47791af0db0b656ccb7229ec7822702a1ffd3</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/PMC6906495/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6906495/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,725,778,782,862,883,27913,27914,41109,42178,51565,53780,53782</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31827150$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ando, Yoshitaka</creatorcontrib><creatorcontrib>Yamazaki, Mirai</creatorcontrib><creatorcontrib>Yamada, Hiroya</creatorcontrib><creatorcontrib>Munetsuna, Eiji</creatorcontrib><creatorcontrib>Fujii, Ryosuke</creatorcontrib><creatorcontrib>Mizuno, Genki</creatorcontrib><creatorcontrib>Ichino, Naohiro</creatorcontrib><creatorcontrib>Osakabe, Keisuke</creatorcontrib><creatorcontrib>Sugimoto, Keiko</creatorcontrib><creatorcontrib>Ishikawa, Hiroaki</creatorcontrib><creatorcontrib>Ohashi, Koji</creatorcontrib><creatorcontrib>Teradaira, Ryoji</creatorcontrib><creatorcontrib>Ohta, Yoshiji</creatorcontrib><creatorcontrib>Hamajima, Nobuyuki</creatorcontrib><creatorcontrib>Hashimoto, Shuji</creatorcontrib><creatorcontrib>Suzuki, Koji</creatorcontrib><title>Association of circulating miR-20a, miR-27a, and miR-126 with non-alcoholic fatty liver disease in general population</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>Non-alcoholic fatty liver disease (NAFLD) is closely associated with obesity, metabolic syndrome, and type II diabetes mellitus. Recently, circulating microRNAs (miRNAs) have been proposed as useful disease biomarkers. We examined whether circulating miRNAs, such as miR-20a, miR-27a, and miR-126, were useful biomarkers for NAFLD. We conducted a cross-sectional analysis of 527 subjects aged 39 years or older who had undergone a health examination in the Yakumo Study. Of the residents, 92 were diagnosed with NAFLD using a registered medical sonographer. Serum miR-20a, miR-27a and miR-126 levels were measured by quantitative real-time PCR. We then calculated the odds ratios for serum miRNA level changes according to the severity of NAFLD using normal liver status as the reference group. Serum levels of miR-20a and 27a, but not miR-126, were significantly lower in NAFLD subjects than normal subjects. Serum miR-20a and miR-27a levels were significantly lower in both male and female severe NAFLD subjects. Logistic regression analysis showed a significant relationship between low circulating miR-20a and 27a levels and severe NAFLD. Down-regulated circulating miR-20a and 27a levels were significantly associated with severe NAFLD in the general population. Circulating miR-20a and miR-27a may be useful biomarkers for severe NAFLD.</description><subject>45</subject><subject>692/308/174</subject><subject>692/53</subject><subject>692/699/1503/1607/2750</subject><subject>Adult</subject><subject>Aged</subject><subject>Biomarkers</subject><subject>Biomarkers - blood</subject><subject>Circulating MicroRNA - blood</subject><subject>Cross-Sectional Studies</subject><subject>Fatty liver</subject><subject>Female</subject><subject>Humanities and Social Sciences</subject><subject>Humans</subject><subject>Japan</subject><subject>Liver diseases</subject><subject>Male</subject><subject>Metabolic disorders</subject><subject>MicroRNAs</subject><subject>MicroRNAs - blood</subject><subject>Middle Aged</subject><subject>multidisciplinary</subject><subject>Non-alcoholic Fatty Liver Disease - blood</subject><subject>Real-Time Polymerase Chain Reaction</subject><subject>Regression analysis</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><issn>2045-2322</issn><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9UU1v3CAQRVWqJkrzB3qokHrJobQDBmwulaJV-iFFqlS1Z4QB7xJ5YQt2ouTXl6zTNM0hXHjDvHkzw0PoDYUPFJruY-FUqI4AVUQIaCW5fYGOGHBBWMPYwSN8iE5KuYR6BFOcqlfosKEda6mAIzSflZJsMFNIEacB25DtPNYwrvE2_CAMzPsFtBWY6PYBZRJfh2mDY4rEjDZt0hgsHsw03eAxXPmMXSjeFI9DxGsffTYj3qXdXjrF1-jlYMbiT-7vY_Tr8_nP1Vdy8f3Lt9XZBbG85RMZhO9833ecS-YYB2nquwMnlaugVdQM4HropZDW9i1jytu2Y6wFZugwuOYYfVp0d3O_9c76ONVB9C6Hrck3Opmg_8_EsNHrdKWlAsmVqAKn9wI5_Z59mfQ2FOvH0USf5qLr_4oGgHdNpb57Qr1Mc451vTsWV9BIxSqLLSybUynZDw_DUNB3xurFWF2N1Xtj9W0tevt4jYeSvzZWQrMQSk3Ftc__ej8j-wcd_q7x</recordid><startdate>20191211</startdate><enddate>20191211</enddate><creator>Ando, Yoshitaka</creator><creator>Yamazaki, Mirai</creator><creator>Yamada, Hiroya</creator><creator>Munetsuna, Eiji</creator><creator>Fujii, Ryosuke</creator><creator>Mizuno, Genki</creator><creator>Ichino, Naohiro</creator><creator>Osakabe, Keisuke</creator><creator>Sugimoto, Keiko</creator><creator>Ishikawa, Hiroaki</creator><creator>Ohashi, Koji</creator><creator>Teradaira, Ryoji</creator><creator>Ohta, Yoshiji</creator><creator>Hamajima, Nobuyuki</creator><creator>Hashimoto, Shuji</creator><creator>Suzuki, Koji</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>C6C</scope><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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20191211</creationdate><title>Association of circulating miR-20a, miR-27a, and miR-126 with non-alcoholic fatty liver disease in general population</title><author>Ando, Yoshitaka ; Yamazaki, Mirai ; Yamada, Hiroya ; Munetsuna, Eiji ; Fujii, Ryosuke ; Mizuno, Genki ; Ichino, Naohiro ; Osakabe, Keisuke ; Sugimoto, Keiko ; Ishikawa, Hiroaki ; Ohashi, Koji ; Teradaira, Ryoji ; Ohta, Yoshiji ; Hamajima, Nobuyuki ; Hashimoto, Shuji ; Suzuki, Koji</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c474t-f5e8ebb84462d2406ac47d0d69dc47791af0db0b656ccb7229ec7822702a1ffd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>45</topic><topic>692/308/174</topic><topic>692/53</topic><topic>692/699/1503/1607/2750</topic><topic>Adult</topic><topic>Aged</topic><topic>Biomarkers</topic><topic>Biomarkers - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ando, Yoshitaka</au><au>Yamazaki, Mirai</au><au>Yamada, Hiroya</au><au>Munetsuna, Eiji</au><au>Fujii, Ryosuke</au><au>Mizuno, Genki</au><au>Ichino, Naohiro</au><au>Osakabe, Keisuke</au><au>Sugimoto, Keiko</au><au>Ishikawa, Hiroaki</au><au>Ohashi, Koji</au><au>Teradaira, Ryoji</au><au>Ohta, Yoshiji</au><au>Hamajima, Nobuyuki</au><au>Hashimoto, Shuji</au><au>Suzuki, Koji</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Association of circulating miR-20a, miR-27a, and miR-126 with non-alcoholic fatty liver disease in general population</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2019-12-11</date><risdate>2019</risdate><volume>9</volume><issue>1</issue><spage>18856</spage><epage>8</epage><pages>18856-8</pages><artnum>18856</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>Non-alcoholic fatty liver disease (NAFLD) is closely associated with obesity, metabolic syndrome, and type II diabetes mellitus. Recently, circulating microRNAs (miRNAs) have been proposed as useful disease biomarkers. We examined whether circulating miRNAs, such as miR-20a, miR-27a, and miR-126, were useful biomarkers for NAFLD. We conducted a cross-sectional analysis of 527 subjects aged 39 years or older who had undergone a health examination in the Yakumo Study. Of the residents, 92 were diagnosed with NAFLD using a registered medical sonographer. Serum miR-20a, miR-27a and miR-126 levels were measured by quantitative real-time PCR. We then calculated the odds ratios for serum miRNA level changes according to the severity of NAFLD using normal liver status as the reference group. Serum levels of miR-20a and 27a, but not miR-126, were significantly lower in NAFLD subjects than normal subjects. Serum miR-20a and miR-27a levels were significantly lower in both male and female severe NAFLD subjects. Logistic regression analysis showed a significant relationship between low circulating miR-20a and 27a levels and severe NAFLD. Down-regulated circulating miR-20a and 27a levels were significantly associated with severe NAFLD in the general population. Circulating miR-20a and miR-27a may be useful biomarkers for severe NAFLD.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>31827150</pmid><doi>10.1038/s41598-019-55076-z</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 45 692/308/174 692/53 692/699/1503/1607/2750 Adult Aged Biomarkers Biomarkers - blood Circulating MicroRNA - blood Cross-Sectional Studies Fatty liver Female Humanities and Social Sciences Humans Japan Liver diseases Male Metabolic disorders MicroRNAs MicroRNAs - blood Middle Aged multidisciplinary Non-alcoholic Fatty Liver Disease - blood Real-Time Polymerase Chain Reaction Regression analysis Science Science (multidisciplinary) |
title | Association of circulating miR-20a, miR-27a, and miR-126 with non-alcoholic fatty liver disease in general population |
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