Expression of miR-210-3p as a Prognostic Marker for Development of Diabetic Neuropathy

TL;DR

This study explores how miR-210-3p gene expression relates to diabetic neuropathy severity and suggests it could help diagnose and monitor the condition.

Contribution

The study identifies miR-210-3p as a potential prognostic marker for diabetic neuropathy when combined with corneal confocal microscopy.

Findings

Lower ΔCt values (higher miR-210-3p expression) were found in patients with combined neuropathy.

miR-210-3p expression was inversely correlated with neuropathy severity but positively with diabetes duration.

Corneal nerve parameters were significantly reduced in diabetic neuropathy patients.

Abstract

Background/Objectives: Diabetic neuropathy (DN) is one of the most common complications of type 2 diabetes mellitus (T2DM), involving complex metabolic, vascular, and epigenetic mechanisms. MicroRNA-210-3p (miR-210-3p), a hypoxia-responsive molecule, has been implicated in various diabetic complications, but its role in DN is not well defined. This study aimed to investigate the relationship between miR-210-3p expression, measured as delta Ct (ΔCt), and the presence and type of diabetic neuropathy, as well as correlations with corneal nerve parameters assessed by corneal confocal microscopy (CCM). Methods: Eighty patients with T2DM were stratified into four groups: no neuropathy, autonomic neuropathy, peripheral neuropathy, and combined neuropathy. Expression of miR-210-3p was quantified using RT-qPCR, and CCM was used to measure corneal nerve fiber density (CNFD), length (CNFL), and branch density (CNBD). Results: ΔCt values were significantly lower in patients with combined neuropathy compared to those without neuropathy, indicating higher miR-210-3p expression. Intermediate values were observed in autonomic and peripheral neuropathy groups. CCM parameters were significantly reduced in patients with DN. ΔCt was inversely correlated with neuropathy severity but positively associated with diabetes duration. Conclusions: These findings suggest that miR-210-3p may serve as a biomarker of nerve damage and cellular stress in diabetes, and that combining gene expression profiling with CCM could improve DN diagnosis and monitoring.

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