Startseite miR-21-3p and miR-192-5p in patients with type 2 diabetic nephropathy
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miR-21-3p and miR-192-5p in patients with type 2 diabetic nephropathy

  • Kadriye Akpınar ORCID logo EMAIL logo , Diler Aslan ORCID logo , Semin Melahat Fenkçi ORCID logo und Vildan Caner ORCID logo
Veröffentlicht/Copyright: 18. August 2022
Diagnosis
Aus der Zeitschrift Diagnosis Band 9 Heft 4

Abstract

Objectives

Microribonucleic acids (microRNA/miRNA/miR-) are predicted to be useful in the early diagnosis, monitoring, and treatment of diabetic nephropathy (DN). We aimed to investigate the relationship of DN to miR-21-3p, miR-29a-3p, miR-29b-3p, miR-29c-3p, miR-126-3p, miR-129-1-3p, miR-137, miR-192-5p, miR-212-3p, and miR-320c.

Methods

There were 50 healthy controls and 100 patients with type 2 diabetes mellitus (T2DM). The diabetic patients were divided into three subgroups: normal to mildly increased (A1, n=51), moderately increased (A2, n=25), and severely increased (A3, n=24) albuminuria. The biochemical measurements were analysed using Roche Cobas 8000. The plasma miRNAs were analysed using RT-qPCR based on SYBR green chemistry.

Results

The relative expression of miR-21-3p was significantly lower in the (A3 p=0.005, 6.6-fold decrease) and DN (A1 + A3) (p=0.005, 6.6-fold decrease) groups compared to the controls. The relative expression of miR-192-5p was also significantly lower in the DN group (p=0.027, 2.4-fold decrease) compared to the controls. The area under curve value was 0.726 for miR-21-3p and 0.717 for miR-192-5p for distinguishing the DN group from the controls.

Conclusions

The decreased expressions of miR-21-3p and miR-192-5p are associated with the development of DN and may be potential biomarkers for the early diagnosis of DN.


Corresponding author: Kadriye Akpınar, Department of Medical Biochemistry, School of Medicine, Pamukkale University, Burdur State Hospital, Biochemistry Laboratory, 15030, Denizli, Burdur, Turkey, E-mail:

Acknowledgments

Grant sponsor: Pamukkale University Scientific Research Projects Department (grant number and date: 2017TIPF018, 26/12/2017).

  1. Research funding: This work was supported by the Pamukkale University Scientific Research Projects Department.

  2. Author contributions: All authors have accepted responsibility for the entire content of this manuscript and approved its submission.

  3. Competing interests: Authors state no conflict of interest.

  4. Informed consent: Informed consent was obtained from all individuals included in this study.

  5. Ethical approval: Research involving human subjects complied with all relevant national regulations, institutional policies and is in accordance with the tenets of the Helsinki Declaration (as revised in 2013), and has been approved by the Research and Ethics Committee of the Medical Faculty of Pamukkale University (approval number: 07; date 16/05/2017).

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Supplementary Material

The online version of this article offers supplementary material (https://doi.org/10.1515/dx-2022-0036).


Received: 2022-04-19
Accepted: 2022-07-23
Published Online: 2022-08-18

© 2022 Walter de Gruyter GmbH, Berlin/Boston

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