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      Clinical association and diagnostic significance of miRNA-29a and miRNA-147b in type 2 diabetes mellitus

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          Abstract

          Background: Micro RNAs (miRs) expression is involved in the pathogenesis of type 2 diabetes mellitus (T2DM). This study investigates the expression levels of plasma miR-29a, miR-146a, and miR-147b and their correlations with clinical parameters in patients with T2DM.

          Methods: 105 patients with T2DM who categorized either as newly diagnosed T2DM (n=52) or treated T2DM (n=53) and 93 healthy individuals were included in this study. The expression levels of miR-29a, miR-146a, and miR-147b were quantified by real-time PCR and analyzed for possible association with T2DM.

          Results: The expressions of miR-29a and miR-147b were significantly increased in T2DM patients compared with healthy controls ( P<0.0001). The expression levels of miR-29a in newly diagnosed T2DM patients were higher than that in the group of treated T2DM ( P=0.002). The expression of studied miRs was correlated with several clinical parameters such as blood glucose levels, HbA1C, microalbuminuria, C-peptide, triglyceride levels as well as the HOMA-β index. The expression levels of miR-29a and miR-147b show a potential diagnostic performance to discriminate newly diagnostic T2DM (AUCs=0.77 and 0.84, respectively) and beta-cell dysfunction (AUCs= 0.62 and 0.75, respectively).

          Conclusions: The plasma miR-29a and miR-147b expression levels in T2DM patients are significantly associated with T2DM while miR-146a shows poor evidence in relation to T2DM. miR-147b shows potential as a biomarker for the diagnosis of T2DM and pancreatic beta cell dysfunction.

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          Analyzing real-time PCR data by the comparative C(T) method.

          Two different methods of presenting quantitative gene expression exist: absolute and relative quantification. Absolute quantification calculates the copy number of the gene usually by relating the PCR signal to a standard curve. Relative gene expression presents the data of the gene of interest relative to some calibrator or internal control gene. A widely used method to present relative gene expression is the comparative C(T) method also referred to as the 2 (-DeltaDeltaC(T)) method. This protocol provides an overview of the comparative C(T) method for quantitative gene expression studies. Also presented here are various examples to present quantitative gene expression data using this method.
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            MicroRNA-29a is up-regulated in beta-cells by glucose and decreases glucose-stimulated insulin secretion.

            Chronically elevated levels of glucose impair pancreatic beta-cell function while inducing beta-cell proliferation. MicroRNA-29a (miR-29a) levels are increased in several tissues in diabetic animals and mediate decreased insulin-stimulated glucose-transport of adipocytes. The aim was to investigate the impact of glucose on miR-29a levels in INS-1E beta-cells and in human islets of Langerhans and furthermore to evaluate the impact of miR-29a on beta-cell function and proliferation. Increased glucose levels up-regulated miR-29a in beta-cells and human and rat islets of Langerhans. Glucose-stimulated insulin-secretion (GSIS) of INS-1E beta-cells was decreased by forced expression of miR-29a, while depletion of endogenous miR-29a improved GSIS. Over-expression of miR-29a increased INS-1E proliferation. Thus, miR-29a up-regulation is involved in glucose-induced proliferation of beta-cells. Furthermore, as depletion of miR-29a improves beta-cell function, miR-29a is a mediator of glucose-induced beta-cell dysfunction. Glucose-induced up-regulation of miR-29a in beta-cells could be implicated in progression from impaired glucose tolerance to type 2 diabetes. Copyright © 2012 Elsevier Inc. All rights reserved.
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              Serum MiR-377 and MiR-29a in Type II Diabetic Patients with Diabetic Nephropathy

              (2016)
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                Author and article information

                Journal
                Int J Med Sci
                Int J Med Sci
                ijms
                International Journal of Medical Sciences
                Ivyspring International Publisher (Sydney )
                1449-1907
                2023
                28 August 2023
                : 20
                : 10
                : 1316-1325
                Affiliations
                [1 ]Endocrine Hospital, Nghe An, Vietnam.
                [2 ]Department of Pathophysiology, Vietnam Military Medical University, Hanoi, Vietnam.
                [3 ]Centre for Genetics Counsulation and Cancer Screening, 108 Military Central Hospital, Hanoi, Vietnam.
                [4 ]Institute of Biomedicine and Pharmacy, Vietnam Military Medical University, Hanoi, Vietnam.
                [5 ]Internal Department, Vinh Medical University, Nghe An, Vietnam.
                [6 ]103 Military Hospital, Vietnam Military Medical University, Hanoi, Vietnam.
                Author notes
                ✉ Corresponding authors: Prof. Nguyen Linh Toan, MD. PhD. Vietnam Military Medical University, 160 Phung Hung Street, Ha Dong, Hanoi, Vietnam; Tel.: +84 979 166 868; E-mail: toannl@ 123456vmmu.edu.vn . Dr. Ngo Tat Trung, PhD. Centre for Genetics Counsulation and Cancer Screening, 108 Military Central Hospital, No 1, Tran Hung Dao Street, Hai Ba Trung Dist, Hanoi, Vietnam; Tel. +84-919119416; Email: tatrungngo@ 123456gmail.com .

                Competing Interests: The authors have declared that no competing interest exists.

                Article
                ijmsv20p1316
                10.7150/ijms.84899
                10542027
                37786444
                bd06dd6e-48c3-4e29-88e1-7f8198be9314
                © The author(s)

                This is an open access article distributed under the terms of the Creative Commons Attribution License ( https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions.

                History
                : 3 April 2023
                : 1 July 2023
                Categories
                Research Paper

                Medicine
                mir-29a,mir-146a,mir-147b,type 2 diabetes mellitus,beta-cell dysfunction
                Medicine
                mir-29a, mir-146a, mir-147b, type 2 diabetes mellitus, beta-cell dysfunction

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