Key result
Urinary exosomal miR-136-5p was significantly elevated in diabetic kidney disease compared to type 2 diabetes, demonstrating diagnostic value with an AUC of 0.722, sensitivity of 72.2%, and specificity of 78.4%.
Why the study?
Diabetic kidney disease is a major cause of chronic and end-stage kidney disease, and exosomal miRNAs play a crucial role in its pathophysiological processes.
Does urinary exosomal miR-136-5p have diagnostic value for identifying diabetic kidney disease in patients with type 2 diabetes?
Case-Control (n=64)
No
Does urinary exosomal miR-136-5p have diagnostic value for identifying diabetic kidney disease in patients with type 2 diabetes?
Effect estimate: AUC 0.722 (95% CI 0.552-0.892)
p-value: p=0.008
Urinary exosomal miR-136-5p is significantly elevated in patients with diabetic kidney disease and may serve as a novel non-invasive diagnostic biomarker.
May support urinary exosomal miRNAs as DKD biomarkers; leaves open prospective validation before clinical use.
Diabetic kidney disease (DKD) has become a major cause of chronic kidney disease and end-stage renal disease. Numerous studies have indicated that exosomal miRNAs play a crucial role in the pathophysiological processes of DKD. We screened differentially expressed miRNAs in urinary exosomes from patients with DKD using the GEO database and performed PCR validation both in patients who were pathologically diagnosed and clinically diagnosed. We assessed the clinical diagnostic value of urinary exosomal miRNAs using ROC curves, analyzed the correlation between miRNAs and clinical indicators, predicted the target genes using the miRTarBase database and explored the potential signaling pathways involved through functional enrichment analysis. Screening results showed that the expression of miR-136-5p was significantly elevated in the DKD group compared to the DM group, with significance maintained in validation samples. The sensitivity and specificity of miR-136-5p for diagnosing DKD were 72.2% and 78.4%, respectively, with an area under the curve of 0.722. Additionally, the expression of miR-136-5p was positively correlated with UACR, urea nitrogen, cystatin C, chronic kidney disease progression risk stratification indicators, and negatively correlated with eGFR. 152 target genes of miR-136-5p were predicted and enriched in 25 pathways, including insulin secretion, cAMP signaling pathway, and sphingolipid signaling pathway.
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Zheng et al. (2025) conducted a case-control in Diabetic kidney disease (n=64). Urinary exosomal miR-136-5p vs. Type 2 diabetes mellitus without diabetic kidney disease was evaluated on Diagnosis of diabetic kidney disease (AUC 0.722, 95% CI 0.552-0.892, p=0.008). Urinary exosomal miR-136-5p was significantly elevated in diabetic kidney disease compared to type 2 diabetes, demonstrating diagnostic value with an AUC of 0.722, sensitivity of 72.2%, and specificity of 78.4%.
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