Zhang Xia, Zhu Mengmeng, Zeng Peng, Guan Mingxiu, Zhang Hongyu, Duan Shaohua, Huang Heli, Liu Yulian, Cong Hongliang, Chen Yuanli
Tianjin Baodi Hospital, Baodi Clinical College of Tianjin Medical University, Tianjin, China.
Key Laboratory of Metabolism and Regulation for Major Diseases of Anhui Higher Education Institutes, College of Food and Biological Engineering, Hefei University of Technology, Hefei, China.
SAGE Open Med. 2024 Aug 18;12:20503121241272646. doi: 10.1177/20503121241272646. eCollection 2024.
Several circulating microRNAs, including microRNA-126-3p, have been identified as diagnostic and prognostic biomarker of cardiovascular disease. However, whether microRNA-126-3p is an independent risk predictor for coronary artery calcification is unclear.
In this prospective single-center study, we collected blood samples from coronary artery atherosclerosis patients ( = 54), patients with coronary artery calcification ( = 33) and controls ( = 56). Total RNA was extracted from plasma and blood cells with TRIzol reagents. The microRNA-126-3p level was determined via quantitative real-time polymerase chain reaction (RT-PCR).
MicroRNA-126-3p levels were significantly increased in patients with coronary artery calcification than in coronary artery atherosclerosis patients or controls. The highest expression of microRNA-126-3p was observed in patients with moderate calcification who were diagnosed with Grade 2 calcification by coronary angiography. Age, microRNA-126-3p expression in veins, hypertension and diabetes significantly influence the occurrence of coronary artery calcification, among which diabetes and venous microRNA-126-3p expression were found to be independent risk factors for coronary artery calcification.
Taken together, the data in this study suggest that circulating microRNA-126-3p may be a novel noninvasive biomarker for coronary artery calcification. Regulating microRNA-126-3p expression may be an effective and promising strategy for the diagnosis and treatment of cardiovascular diseases, especially coronary artery calcification.
包括微小RNA - 126 - 3p在内的几种循环微小RNA已被确定为心血管疾病的诊断和预后生物标志物。然而,微小RNA - 126 - 3p是否为冠状动脉钙化的独立风险预测因子尚不清楚。
在这项前瞻性单中心研究中,我们收集了冠状动脉粥样硬化患者(n = 54)、冠状动脉钙化患者(n = 33)和对照组(n = 56)的血样。使用TRIzol试剂从血浆和血细胞中提取总RNA。通过定量实时聚合酶链反应(RT-PCR)测定微小RNA - 126 - 3p水平。
冠状动脉钙化患者的微小RNA - 126 - 3p水平显著高于冠状动脉粥样硬化患者或对照组。在冠状动脉造影诊断为2级钙化的中度钙化患者中观察到微小RNA - 126 - 3p的最高表达。年龄、静脉中微小RNA - 126 - 3p表达、高血压和糖尿病显著影响冠状动脉钙化的发生,其中糖尿病和静脉微小RNA - 126 - 3p表达是冠状动脉钙化的独立危险因素。
综上所述,本研究数据表明循环微小RNA - 126 - 3p可能是冠状动脉钙化的一种新型非侵入性生物标志物。调节微小RNA - 126 - 3p表达可能是诊断和治疗心血管疾病,尤其是冠状动脉钙化的有效且有前景的策略。