Yao S Y, Liu J, Li Y, Wang M, Wang C, Xue H
Department of Cardiology, People's Liberition Army General Hospital, Beijing 100853, China.
Medicine School of Nankai Uninversity, Tianjin 300071, China.
Zhonghua Xin Xue Guan Bing Za Zhi. 2019 Mar 24;47(3):215-220. doi: 10.3760/cma.j.issn.0253-3758.2019.03.007.
Previous studies have shown that plasma microRNA-29a (miRNA-29a) is associated with myocardial fibrosis and the degree of cardiac hypertrophy in patients with hypertrophic cardiomyopathy. However, the relationship between plasma miRNA-29a and hypertensive left ventricular hypertrophy (LVH) has not yet been reported. So the purpose of this study is to investigate the relationship between the plasma miRNA-29a and hypertensive LVH. Enrolled 168 hypertensive patients and classified the patients into 2 groups: those with LVH (LVH group, 41) and those without LVH (NLVH group, 127). All patients underwent echocardiography examination. Left ventricular mass index (LVMI) was calculated by interventricular septal thickness (IVSd), left ventricular posterior wall thickness(LVPWTd), left ventricular end diastolic dimension (LVEDD) and left ventricular mass index (LVMI) were obtained. Plasma levels of miRNA-29a were assessed by quantitative real-time polymerase chain reaction (qRT-PCR). The relationship between plasma miRNA-29a levels and LVH was analyzed. Plasma miRNA-29a was significantly higher in LVH group than in NLVH group (0.52±0.10 vs. 0.37±0.07, 9.788, 0.01) . Pearson correlation analysis evidenced a positive correlation between plasma miRNA-29a levels and IVSd(=0.459, 0.01), LVPWTd (=0.398, 0.01), and LVMI (=0.745, 0.01). After adjustment for gender, age, systolic blood pressure, diastolic blood pressure, body mass index, hypertension duration, antihypertensive drugs, multiple regression analysis showed that there were still positive correlations between plasma miRNA-29a level and IVSd (β=0.535, 0.01), LVPWTd (β=0.085, 0.01), and LVMI (β=0.806, 0.01). Plasma miRNA-29a level is positively associated with LVH in hypertensive patients, and future studies are warranted to explore if miRNA-29a could be used as a potential biomarker for LVH assessment in hypertensive patients.
既往研究表明,血浆微小RNA-29a(miRNA-29a)与肥厚型心肌病患者的心肌纤维化及心脏肥厚程度相关。然而,血浆miRNA-29a与高血压性左心室肥厚(LVH)之间的关系尚未见报道。因此,本研究旨在探讨血浆miRNA-29a与高血压性LVH之间的关系。纳入168例高血压患者,并将其分为2组:LVH组(41例)和非LVH组(127例)。所有患者均接受超声心动图检查。通过室间隔厚度(IVSd)、左心室后壁厚度(LVPWTd)计算左心室质量指数(LVMI),并获取左心室舒张末期内径(LVEDD)和左心室质量指数(LVMI)。采用定量实时聚合酶链反应(qRT-PCR)评估血浆miRNA-29a水平。分析血浆miRNA-29a水平与LVH的关系。LVH组血浆miRNA-29a水平显著高于非LVH组(0.52±0.10对0.37±0.07,9.788,0.01)。Pearson相关性分析表明,血浆miRNA-29a水平与IVSd(r=0.459,P=0.01)、LVPWTd(r=0.398,P=0.01)和LVMI(r=0.745,P=0.01)呈正相关。在对性别、年龄、收缩压、舒张压、体重指数、高血压病程、降压药物进行校正后,多元回归分析显示血浆miRNA-29a水平与IVSd(β=0.535,P=0.01)、LVPWTd(β=0.085,P=0.01)和LVMI(β=0.806,P=0.01)仍呈正相关。高血压患者血浆miRNA-29a水平与LVH呈正相关,未来有必要进行研究以探索miRNA-29a是否可作为高血压患者LVH评估的潜在生物标志物。