Sex differences in plasma MicroRNA biomarkers of early and complicated diabetes mellitus in Israeli Arab and jewish patients

Ari Meerson, Azwar Najjar, Elias Saad, Wisam Sbeit, Masad Barhoum, Nimer Assy

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19 Scopus citations

Abstract

MicroRNAs play functional roles in the etiology of type 2 diabetes mellitus (T2DM) and complications, and extracellular microRNAs have attracted interest as potential biomarkers of these conditions. We aimed to identify a set of plasma microRNAs, which could serve as biomarkers of T2DM and complications in a mixed Israeli Arab/Jewish patient sample. Subjects included 30 healthy volunteers, 29 early-stage T2DM patients, and 29 late-stage T2DM patients with renal and/or vascular complications. RNA was isolated from plasma, and the levels of 12 candidate microRNAs were measured by quantitative reverse transcription and polymerase chain reaction (qRT-PCR). MicroRNA levels were compared between the groups and correlated to clinical measurements, followed by stepwise regression analysis and discriminant analysis. Plasma miR-486-3p and miR-423 were respectively up- and down-regulated in T2DM patients compared to healthy controls. MiR-28-3p and miR-423 were up-regulated in patients with complicated T2DM compared to early T2DM, while miR-486-3p was down-regulated. Combined, four microRNAs (miR-146a-5p, miR-16-2-3p, miR-126-5p, and miR-30d) could distinguish early from complicated T2DM with 77% accuracy and 79% sensitivity. In male patients only, the same microRNAs, with the addition of miR-423, could distinguish early from complicated T2DM with 83.3% accuracy. Furthermore, plasma microRNA levels showed significant correlations with clinical measurements, and these differed between men and women. Additionally, miR-183-5p levels differed significantly between the ethnic groups. Our study identified a panel of specific plasma microRNAs which can serve as biomarkers of T2DM and its complications and emphasizes the importance of sex differences in their clinical application.

Original languageEnglish
Article number32
JournalNon-coding RNA
Volume5
Issue number2
DOIs
StatePublished - 5 Apr 2019

Bibliographical note

Publisher Copyright:
© 2018 by the authors.

Funding

Funding: This research was funded by a Diabetes Research Grant from D-Cure and the Ministry of Health, Israel, to AM, and by the European Union’s FP7-REGPOT-2012-2013-1, Agreement No 316157 (“CEREHA”). We thank Hila Yehuda, MIGAL and Nelly Bar-Guy, Galilee Medical Center for skilled technical and administrative assistance. This research was funded by a Diabetes Research Grant from D-Cure and the Ministry of Health, Israel, to AM, and by the European Union's FP7-REGPOT-2012-2013-1, Agreement No 316157 ("CEREHA")

FundersFunder number
Diabetes
European Union's FP7-REGPOT-2012-2013-1
Seventh Framework Programme316157
European CommissionFP7-REGPOT-2012-2013-1
Ministry of Health, State of Israel

    Keywords

    • Biomarkers
    • Blood-borne
    • Complications
    • Diabetes mellitus
    • Extracellular
    • MicroRNAs
    • Sex differences

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