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Comparisons of serum miRNA expression profiles in patients with diabetic retinopathy and type 2 diabetes mellitus.

Authors :
Ma J
Wang J
Liu Y
Wang C
Duan D
Lu N
Wang K
Zhang L
Gu K
Chen S
Zhang T
You D
Han L
Source :
Clinics (Sao Paulo, Brazil) [Clinics (Sao Paulo)] 2017 Feb 01; Vol. 72 (2), pp. 111-115. Date of Electronic Publication: 2017 Feb 01.
Publication Year :
2017

Abstract

Objectives:: The aim of this study was to compare the expression levels of serum miRNAs in diabetic retinopathy and type 2 diabetes mellitus.<br />Methods:: Serum miRNA expression profiles from diabetic retinopathy cases (type 2 diabetes mellitus patients with diabetic retinopathy) and type 2 diabetes mellitus controls (type 2 diabetes mellitus patients without diabetic retinopathy) were examined by miRNA-specific microarray analysis. Quantitative real-time polymerase chain reaction was used to validate the significantly differentially expressed serum miRNAs from the microarray analysis of 45 diabetic retinopathy cases and 45 age-, sex-, body mass index- and duration-of-diabetes-matched type 2 diabetes mellitus controls. The relative changes in serum miRNA expression levels were analyzed using the 2-ΔΔCt method.<br />Results:: A total of 5 diabetic retinopathy cases and 5 type 2 diabetes mellitus controls were included in the miRNA-specific microarray analysis. The serum levels of miR-3939 and miR-1910-3p differed significantly between the two groups in the screening stage; however, quantitative real-time polymerase chain reaction did not reveal significant differences in miRNA expression for 45 diabetic retinopathy cases and their matched type 2 diabetes mellitus controls.<br />Conclusion:: Our findings indicate that miR-3939 and miR-1910-3p may not play important roles in the development of diabetic retinopathy; however, studies with a larger sample size are needed to confirm our findings.

Details

Language :
English
ISSN :
1980-5322
Volume :
72
Issue :
2
Database :
MEDLINE
Journal :
Clinics (Sao Paulo, Brazil)
Publication Type :
Academic Journal
Accession number :
28273235
Full Text :
https://doi.org/10.6061/clinics/2017(02)08