Serum miR-377-3p levels were significantly lower in carotid artery stenosis patients, demonstrating high diagnostic value with an AUC of 0.9597.
Does serum miR-377-3p have diagnostic value for carotid artery stenosis?
Serum miR-377-3p is significantly downregulated in patients with carotid artery stenosis and demonstrates high diagnostic accuracy, while also inhibiting vascular smooth muscle cell proliferation and migration by targeting EDIL3.
Absolute Event Rate: 0% vs 0%
Purpose: To determine the serum expression profile of miR-377-3p in carotid artery stenosis (CAS) patients and to assess its diagnostic potential in a clinical setting. Patients and Methods: Using qRT-PCR, miR-377-3p expression was measured in serum samples from 78 CAS patients and 78 matched healthy controls. We used the Pearson correlation to analyze inter-indicator relationships and the ROC curve to assess the diagnostic significance of miR-377-3p. The cellular functions of human aortic smooth muscle cells (HASMCs) were assessed. Bioinformatics predictions of target associations were experimentally verified with a luciferase activity assay. Results: Patients diagnosed with CAS had a lower serum level of miR-377-3p. ROC curve-based analysis showed that miR-377-3p exerted high diagnostic value, where the area under the curve (AUC) was 0.9597. Serum miR-377-3p was negatively correlated with systolic blood pressure (SBP), diastolic blood pressure (DBP), fasting blood glucose (FBG), and low-density lipoprotein cholesterol (LDL), while positively correlated with high-density lipoprotein cholesterol (HDL). miR-377-3p inhibited the proliferation and migration of HASMCs, but this effect was counteracted by EDIL3. Conclusion: These results suggest the dual utility of miR-377-3p as a promising biomarker and a potential therapeutic target in the management of CAS. miR-377-3p can inhibit the proliferation and migration of HASMCs by targeting EDIL3.
Qie et al. (Thu,) reported a other. Serum miR-377-3p levels were significantly lower in carotid artery stenosis patients, demonstrating high diagnostic value with an AUC of 0.9597.
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