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Increased MicroRNA-146a Levels in Plasma of Patients with Newly Diagnosed Type 2 Diabetes Mellitus

BACKGROUND: MicroRNAs (miRNAs), a class of small non-coding RNAs, are thought to serve as crucial regulators of gene expression. Dysregulated expression of miRNAs has been described in various diseases and may contribute to related pathologic processes. Our aim was to examine circulating miRNA-146a...

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Autores principales: Rong, Ying, Bao, Wei, Shan, Zhilei, Liu, Jun, Yu, Xuefeng, Xia, Songfan, Gao, Hui, Wang, Xia, Yao, Ping, Hu, Frank B., Liu, Liegang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3759444/
https://www.ncbi.nlm.nih.gov/pubmed/24023848
http://dx.doi.org/10.1371/journal.pone.0073272
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author Rong, Ying
Bao, Wei
Shan, Zhilei
Liu, Jun
Yu, Xuefeng
Xia, Songfan
Gao, Hui
Wang, Xia
Yao, Ping
Hu, Frank B.
Liu, Liegang
author_facet Rong, Ying
Bao, Wei
Shan, Zhilei
Liu, Jun
Yu, Xuefeng
Xia, Songfan
Gao, Hui
Wang, Xia
Yao, Ping
Hu, Frank B.
Liu, Liegang
author_sort Rong, Ying
collection PubMed
description BACKGROUND: MicroRNAs (miRNAs), a class of small non-coding RNAs, are thought to serve as crucial regulators of gene expression. Dysregulated expression of miRNAs has been described in various diseases and may contribute to related pathologic processes. Our aim was to examine circulating miRNA-146a levels in newly diagnosed type 2 diabetes mellitus (new-T2DM) patients from a Chinese Han population. METHODOLOGY/PRINCIPAL FINDINGS: Circulating miRNA-146a was extracted from plasma samples of 90 new-T2DM patients and 90 age- and sex-matched controls. Quantitative PCR assessment revealed that circulating miRNA-146a levels were significantly elevated in new-T2DM patients compared with controls. Participants in the highest tertile of circulating miRNA-146a levels showed a notably higher risk for new-T2DM (crude OR 4.333, 95% CI, 1.935 to 9.705, P = 0.001) than persons in the lowest tertile. Controlling for known risk factors and some biochemical indicators did not attenuate the aforementioned association. In addition, receiver operating characteristic (ROC) curves generated for miRNA-146a revealed an area under the curve (AUC) of 0.725 (95% CI, 0.651 to 0.799, P < 0.001). Moreover, higher circulating miRNA-146a levels were significantly associated with higher plasma heme oxygenase-1 (HO-1) concentrations (β coefficient = 0.131, P < 0.001) and lower HOMA-beta (β coefficient = -0.153, P = 0.015). CONCLUSIONS/SIGNIFICANCE: We found that circulating miRNA-146a levels were significantly elevated in new-T2DM patients compared with healthy controls. Whether expression of circulating miRNA-146a holds predictive value for T2DM warrants further investigations.
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spelling pubmed-37594442013-09-10 Increased MicroRNA-146a Levels in Plasma of Patients with Newly Diagnosed Type 2 Diabetes Mellitus Rong, Ying Bao, Wei Shan, Zhilei Liu, Jun Yu, Xuefeng Xia, Songfan Gao, Hui Wang, Xia Yao, Ping Hu, Frank B. Liu, Liegang PLoS One Research Article BACKGROUND: MicroRNAs (miRNAs), a class of small non-coding RNAs, are thought to serve as crucial regulators of gene expression. Dysregulated expression of miRNAs has been described in various diseases and may contribute to related pathologic processes. Our aim was to examine circulating miRNA-146a levels in newly diagnosed type 2 diabetes mellitus (new-T2DM) patients from a Chinese Han population. METHODOLOGY/PRINCIPAL FINDINGS: Circulating miRNA-146a was extracted from plasma samples of 90 new-T2DM patients and 90 age- and sex-matched controls. Quantitative PCR assessment revealed that circulating miRNA-146a levels were significantly elevated in new-T2DM patients compared with controls. Participants in the highest tertile of circulating miRNA-146a levels showed a notably higher risk for new-T2DM (crude OR 4.333, 95% CI, 1.935 to 9.705, P = 0.001) than persons in the lowest tertile. Controlling for known risk factors and some biochemical indicators did not attenuate the aforementioned association. In addition, receiver operating characteristic (ROC) curves generated for miRNA-146a revealed an area under the curve (AUC) of 0.725 (95% CI, 0.651 to 0.799, P < 0.001). Moreover, higher circulating miRNA-146a levels were significantly associated with higher plasma heme oxygenase-1 (HO-1) concentrations (β coefficient = 0.131, P < 0.001) and lower HOMA-beta (β coefficient = -0.153, P = 0.015). CONCLUSIONS/SIGNIFICANCE: We found that circulating miRNA-146a levels were significantly elevated in new-T2DM patients compared with healthy controls. Whether expression of circulating miRNA-146a holds predictive value for T2DM warrants further investigations. Public Library of Science 2013-09-02 /pmc/articles/PMC3759444/ /pubmed/24023848 http://dx.doi.org/10.1371/journal.pone.0073272 Text en © 2013 Rong et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Rong, Ying
Bao, Wei
Shan, Zhilei
Liu, Jun
Yu, Xuefeng
Xia, Songfan
Gao, Hui
Wang, Xia
Yao, Ping
Hu, Frank B.
Liu, Liegang
Increased MicroRNA-146a Levels in Plasma of Patients with Newly Diagnosed Type 2 Diabetes Mellitus
title Increased MicroRNA-146a Levels in Plasma of Patients with Newly Diagnosed Type 2 Diabetes Mellitus
title_full Increased MicroRNA-146a Levels in Plasma of Patients with Newly Diagnosed Type 2 Diabetes Mellitus
title_fullStr Increased MicroRNA-146a Levels in Plasma of Patients with Newly Diagnosed Type 2 Diabetes Mellitus
title_full_unstemmed Increased MicroRNA-146a Levels in Plasma of Patients with Newly Diagnosed Type 2 Diabetes Mellitus
title_short Increased MicroRNA-146a Levels in Plasma of Patients with Newly Diagnosed Type 2 Diabetes Mellitus
title_sort increased microrna-146a levels in plasma of patients with newly diagnosed type 2 diabetes mellitus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3759444/
https://www.ncbi.nlm.nih.gov/pubmed/24023848
http://dx.doi.org/10.1371/journal.pone.0073272
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