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Expression of serum microRNA 30e-5p in type 2 diabetic patients with diabetic kidney disease
Raghda E Ibrahim1, Shymaa O A Khalil1, Khadiga Abougabal1
1Department of Clinical and Chemical Pathology, Faculty of Medicine, Beni-Suef University, , Beni-Suef, Egypt.
Abstract:
Type 2 diabetes (T2DM) is the most prevalent form of diabetes, and frequently associated with diabetic nephropathy, a leading contributor to chronic kidney disease (CKD). The presence of microalbuminuria serves as an early marker for diabetic kidney disease (DKD). Emerging evidence suggested that alterations in microRNA (miRNA) 30e-5p expression may be linked to T2DM progression, positioning it as a potential biomarker. This study investigated the clinical relevance of miRNA 30e-5p dysregulation by assessing its expression levels in T2DM patients with and without DKD. A total of 50 participants, including 25 T2DM patients with DKD and 25 T2DM patients without DKD, were examined. Serum miRNA 30e-5p levels were quantified using real-time polymerase chain reaction. Findings revealed a significant reduction in miRNA 30e-5p expression among patients with DKD compared to those without DKD (0.25 ± 0.26 vs. 0.89 ± 0.13, p < 0.001). In conclusion, miRNA 30e-5p dysregulation appears to contribute to DKD development in Egyptian T2DM patients, suggesting its potential as a prognostic biomarker.
Insights
Reduced microRNA 30e-5p expression is linked to diabetic kidney disease (DKD) in Egyptian type 2 diabetes (T2DM) patients. This finding suggests miRNA 30e-5p may serve as a prognostic biomarker for DKD development.
Area of Science:
- Endocrinology
- Molecular Biology
- Nephrology
Background:
- Type 2 diabetes (T2DM) is a leading cause of chronic kidney disease (CKD), with diabetic kidney disease (DKD) being a major complication.
- Microalbuminuria is an early indicator of DKD.
- MicroRNA (miRNA) 30e-5p dysregulation is implicated in T2DM progression and may act as a biomarker.
Purpose of the Study:
- To investigate the clinical significance of miRNA 30e-5p dysregulation in T2DM patients.
- To assess serum miRNA 30e-5p expression levels in T2DM patients with and without DKD.
Main Methods:
- Real-time polymerase chain reaction was used to quantify serum miRNA 30e-5p levels.
- The study included 50 participants: 25 T2DM patients with DKD and 25 T2DM patients without DKD.
Main Results:
- Serum miRNA 30e-5p levels were significantly lower in T2DM patients with DKD compared to those without DKD (0.25 ± 0.26 vs. 0.89 ± 0.13, p < 0.001).
Conclusions:
- miRNA 30e-5p dysregulation is associated with DKD development in Egyptian T2DM patients.
- miRNA 30e-5p shows potential as a prognostic biomarker for DKD.
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