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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Veröffentlicht in:Scientific reports 2019-12, Vol.9 (1), p.18856-8, Article 18856
Hauptverfasser: 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
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container_end_page 8
container_issue 1
container_start_page 18856
container_title Scientific reports
container_volume 9
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.
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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. 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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. 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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.</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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