Iacobescu Loredana, Ciobanu Andrea Olivia, Macarie Razvan, Vadana Mihaela, Ciortan Letitia, Tucureanu Monica Madalina, Butoi Elena, Simionescu Maya, Vinereanu Dragos
Department of Cardiology, University of Medicine and Pharmacy Carol Davila, Dionisie Lupu Street, 126900 Bucharest, Romania.
University and Emergency Hospital, Splaiul Independentei 169, 050098 Bucharest, Romania.
Curr Issues Mol Biol. 2024 Aug 3;46(8):8499-8511. doi: 10.3390/cimb46080500.
Recent studies reported that circulating microRNAs (miRNAs) can target different metalloproteases (MMPs) involved in matrix remodeling and plaque vulnerability. Consequently, they might have a role in the diagnosis and prognosis of coronary artery disease. To quantify circulating miRNAs (miRNA126, miRNA146, and miRNA21) suggested to have possible cardiovascular implications, as well as levels of MMP-1 and MMP-9, and to determine their association with left ventricular (LV) function and with arterial function, in patients with either ST-segment elevation acute myocardial infarction (STEMI) or stable ischemic heart disease (SIHD). A total of 90 patients with coronary artery disease (61% men, 58 ± 12 years), including 60 patients with STEMI and 30 patients with SIHD, were assessed within 24 h of admission, by measuring serum microRNAs, and serum MMP-1 and MMP-9. LV function was assessed by measuring ejection fraction (EF) by 2D and 3D echocardiography, and global longitudinal strain (GLS) by speckle tracking. Arterial function was assessed by echo tracking, CAVI, and peripheral Doppler. Circulating levels of miRNA146, miRNA21, and MMP1 were significantly increased in patients with STEMI vs. SIHD ( = 0.0001, = 0.0001, = 0.04, respectively). MiRNA126 negatively correlated with LVEF (r = -0.33, = 0.01) and LV deformation parameters (r = -0.31, = 0.03) in patients with STEMI and negatively correlated with ABI parameters (r = -0.39, = 0.03, r = -0.40, = 0.03, respectively) in patients with SIHD. MiRNA146 did not have any significant correlations, while higher values of miRNA21 were associated with lower values of GLS in STEMI patients and with higher values of GLS in SIHD patients. Both MMP1 and MMP9 correlated negatively with LVEF (r = -0.27, = 0.04, r = -0.40, = 0.001, respectively) and GLS in patients with STEMI, and positively with arterial stiffness in patients with SIHD (r = 0.40 and r = 0.32, respectively; both < 0.05). MiRNA126, miRNA21, and both MMP1 and MMP9 are associated with LV and arterial function parameters in patients with acute coronary syndrome. Meanwhile, they inversely correlate with arterial function in patients with chronic atherosclerotic disease. However, further studies are needed to establish whether these novel biomarkers have diagnosis and prognosis significance.
近期研究报道,循环微RNA(miRNA)可靶向参与基质重塑和斑块易损性的不同金属蛋白酶(MMP)。因此,它们可能在冠状动脉疾病的诊断和预后中发挥作用。为了量化提示可能具有心血管影响的循环miRNA(miRNA126、miRNA146和miRNA21)以及MMP-1和MMP-9的水平,并确定它们与ST段抬高型急性心肌梗死(STEMI)或稳定型缺血性心脏病(SIHD)患者左心室(LV)功能及动脉功能的关联。共纳入90例冠状动脉疾病患者(男性占61%,年龄58±12岁),其中包括60例STEMI患者和30例SIHD患者,在入院后24小时内通过检测血清微RNA、血清MMP-1和MMP-9进行评估。通过二维和三维超声心动图测量射血分数(EF)以及通过斑点追踪测量整体纵向应变(GLS)来评估LV功能。通过回声追踪、CAVI和外周多普勒评估动脉功能。与SIHD患者相比,STEMI患者中miRNA146、miRNA21和MMP1的循环水平显著升高(分别为P = 0.0001、P = 0.0001、P = 0.04)。在STEMI患者中,miRNA126与左心室射血分数(LVEF)呈负相关(r = -0.33,P = 0.01)以及与LV变形参数呈负相关(r = -0.31,P = 0.03);在SIHD患者中,miRNA126与ABI参数呈负相关(分别为r = -0.39,P = 0.03;r = -0.40,P = 0.03)。miRNA146无任何显著相关性,而在STEMI患者中miRNA21值越高与GLS值越低相关,在SIHD患者中则与GLS值越高相关。在STEMI患者中,MMP1和MMP9均与LVEF呈负相关(分别为r = -0.27,P = 0.04;r = -0.40,P = 0.001)以及与GLS呈负相关,在SIHD患者中与动脉僵硬度呈正相关(分别为r = 0.40和r = 0.32;均P < 0.05)。miRNA126、miRNA21以及MMP1和MMP9均与急性冠状动脉综合征患者的LV和动脉功能参数相关。同时,它们与慢性动脉粥样硬化疾病患者的动脉功能呈负相关。然而,需要进一步研究来确定这些新型生物标志物是否具有诊断和预后意义。