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The rs2910164 variant is associated with reduced miR-146a expression but not cytokine levels in patients with type 2 diabetes

Authors :
Alipoor, B.
Ghaedi, H.
Meshkani, R.
Omrani, M.
Sharifi, Z.
Golmohammadi, T.
Source :
Journal of Endocrinological Investigation; May 2018, Vol. 41 Issue: 5 p557-566, 10p
Publication Year :
2018

Abstract

Previous reports have demonstrated that genetic variations in microRNAs regulome could affect microRNAs-mediated regulation. Therefore, in the present study we were aimed at (1) comparison of microRNA 146-a (miR-146a) peripheral blood mononuclear cells (PBMCs) and plasma levels between diabetic patients and controls, and (2) investigating the possible association of rs2910164 with miR-146a and its related target genes expression and also serum cytokine levels. The study population consisted of 60 subjects including 30 type 2 diabetes (T2D) patients and 30 controls with determined genotypes for rs2910164. The RNA expression levels were determined by real-time PCR. Moreover, TNF-α, IL-6, IL-10 and IL-1β serum levels were measured using ELISA method. Our results showed that the miR-146a expression levels were significantly decreased in PBMCs (P= 0.004) and plasma (P= 0.008) samples of patients with T2D compared to healthy participants. In addition, we observed that IRAK1mRNA expression—but not TLR4, TRAF6and NFĸB—was significantly increased in patients with T2D compared to controls (P= 0.028). The relative expression levels of miR-146a in plasma and PBMCs samples of diabetic patients with the rs2910164 GG genotypes were significantly higher than that in CC (P< 0.05). Moreover, no significant differences were found in miR-146a targets and cytokine levels between the rs2910164 different genotypes. Our study demonstrated that miR-146a circulating levels were significantly elevated in controls compared with T2D patients. In addition, we identified that rs2910164-C allele is associated with reduced expression levels of the miR-146a but not its mRNAs targets and cytokine levels in diabetic patients.

Details

Language :
English
ISSN :
03914097 and 17208386
Volume :
41
Issue :
5
Database :
Supplemental Index
Journal :
Journal of Endocrinological Investigation
Publication Type :
Periodical
Accession number :
ejs44746383
Full Text :
https://doi.org/10.1007/s40618-017-0766-z