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Let-7a-5p在原发性高血压中的诊断价值

Diagnostic Value of Let-7a-5p in Essential Hypertension.

作者信息

Wang Lan, Zhu Qianqian, Cheng Bin, Jiang Nan, Dong Changwu

机构信息

Anhui University of Traditional Chinese Medicine, Anhui, China.

The Second Affiliated Hospital of Anhui University of Traditional Chinese Medicine, Anhui, China.

出版信息

J Clin Hypertens (Greenwich). 2025 Mar;27(3):e70033. doi: 10.1111/jch.70033.

Abstract

This study aimed to investigate the role of let-7a-5p in the pathogenesis of essential hypertension (EH) and its correlation with the renin-angiotensin-aldosterone system (RAAS) biomarkers. Ninety-eight EH patients and 24 healthy controls (HC) enrolled in the study were assayed for the relative expression of let-7a-5p in plasma by quantitative real-time polymerase chain reaction (Q-PCR), and biomarkers of the RAAS system, including angiotensin-converting enzyme 2 (ACE2), Ang (1-7), MAS1, angiotensin-converting enzyme (ACE), angiotensin II (Ang II), and angiotensin II type 1 receptor (AT1R), were determined by enzyme-linked immunosorbent assay (ELISA) The expression levels of the biomarkers of RAAS system were determined. The results showed that the expression levels of let-7a-5p in the plasma of EH patients were remarkably higher than those of HC. The prediction model of combined let-7a-5p showed high accuracy by constructing a subject operating characteristic (ROC) curve with an area under the curve (AUC) of 0.885, and the reliability of the model was further verified by the Hosmer-Lemeshow (H-L) goodness-of-fit test, the Model Calibration Curve, and the Decision Curve Analysis. Spearman correlation analysis revealed that the expression of let-7a-5p was positively correlated with ACE (r = 0.352, p < 0.001), and mediation analysis indicated that ACE partially mediated between let-7a-5p and the development of hypertension. The present study concludes with the potential of let-7a-5p as a companion diagnostic biomarker for EH. It suggests that there may be a complex regulatory mechanism between it and specific RAAS biomarkers, which provides a new perspective on the pathogenesis and diagnosis of EH.

摘要

本研究旨在探讨let-7a-5p在原发性高血压(EH)发病机制中的作用及其与肾素-血管紧张素-醛固酮系统(RAAS)生物标志物的相关性。对纳入本研究的98例EH患者和24例健康对照(HC),采用定量实时聚合酶链反应(Q-PCR)检测血浆中let-7a-5p的相对表达,并通过酶联免疫吸附测定(ELISA)法检测RAAS系统的生物标志物,包括血管紧张素转换酶2(ACE2)、血管紧张素(1-7)、MAS1、血管紧张素转换酶(ACE)、血管紧张素II(Ang II)和血管紧张素II 1型受体(AT1R),并测定RAAS系统生物标志物的表达水平。结果显示,EH患者血浆中let-7a-5p的表达水平显著高于HC。通过构建受试者工作特征(ROC)曲线,曲线下面积(AUC)为0.885,联合let-7a-5p的预测模型显示出较高的准确性,并且通过Hosmer-Lemeshow(H-L)拟合优度检验、模型校准曲线和决策曲线分析进一步验证了该模型的可靠性。Spearman相关性分析显示,let-7a-5p的表达与ACE呈正相关(r = 0.352,p < 0.001),中介分析表明ACE在let-7a-5p与高血压发生之间起部分中介作用。本研究得出结论,let-7a-5p具有作为EH伴随诊断生物标志物的潜力。这表明它与特定RAAS生物标志物之间可能存在复杂的调节机制,为EH的发病机制和诊断提供了新的视角。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2a1/11932552/2327f6bfbb47/JCH-27-e70033-g005.jpg

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