Úri Katalin, Fagyas Miklós, Mányiné Siket Ivetta, Kertész Attila, Csanádi Zoltán, Sándorfi Gábor, Clemens Marcell, Fedor Roland, Papp Zoltán, Édes István, Tóth Attila, Lizanecz Erzsébet
Division of Clinical Physiology, Institute of Cardiology, Medical and Health Science Centre, University of Debrecen, Debrecen, Hungary.
Institute of Cardiology, Medical and Health Science Centre, University of Debrecen, Debrecen, Hungary.
PLoS One. 2014 Apr 1;9(4):e87845. doi: 10.1371/journal.pone.0087845. eCollection 2014.
Growing evidence exists for soluble Angiotensin Converting Enzyme-2 (sACE2) as a biomarker in definitive heart failure (HF), but there is little information about changes in sACE2 activity in hypertension with imminent heart failure and in reverse remodeling.
METHODS, FINDINGS: Patients with systolic HF (NYHAII-IV, enrolled for cardiac resynchronisation therapy, CRT, n = 100) were compared to hypertensive patients (n = 239) and to a healthy cohort (n = 45) with preserved ejection fraction (EF>50%) in a single center prospective clinical study. The status of the heart failure patients were checked before and after CRT. Biochemical (ACE and sACE2 activity, ACE concentration) and echocardiographic parameters (EF, left ventricular end-diastolic (EDD) and end-systolic diameter (ESD) and dP/dt) were measured. sACE2 activity negatively correlated with EF and positively with ESD and EDD in all patient's populations, while it was independent in the healthy cohort. sACE2 activity was already increased in the hypertensive group, where signs for imminent heart failure (slightly decreased EF and barely increased NT-proBNP levels) were detected. sACE2 activities further increased in patients with definitive heart failure (EF<50%), while sACE2 activities decreased with the improvement of the heart failure after CRT (reverse remodeling). Serum angiotensin converting enzyme (ACE) concentrations were lower in the diseased populations, but did not show a strong correlation with the echocardiographic parameters.
Soluble ACE2 activity appears to be biomarker in heart failure, and in hypertension, where heart failure may be imminent. Our data suggest that sACE2 is involved in the pathomechanism of hypertension and HF.
越来越多的证据表明,可溶性血管紧张素转换酶2(sACE2)作为终末期心力衰竭(HF)的生物标志物,但关于即将发生心力衰竭的高血压患者以及逆向重构过程中sACE2活性变化的信息却很少。
方法、研究结果:在一项单中心前瞻性临床研究中,将收缩性心力衰竭患者(纽约心脏协会II-IV级,入选心脏再同步治疗,CRT,n = 100)与高血压患者(n = 239)以及射血分数保留(EF>50%)的健康队列(n = 45)进行比较。在CRT前后检查心力衰竭患者的状态。测量生化指标(ACE和sACE2活性、ACE浓度)和超声心动图参数(EF、左心室舒张末期内径(EDD)和收缩末期内径(ESD)以及dP/dt)。在所有患者群体中,sACE2活性与EF呈负相关,与ESD和EDD呈正相关,而在健康队列中则无相关性。高血压组中sACE2活性已经升高,在该组中检测到即将发生心力衰竭的迹象(EF略有下降且NT-proBNP水平略有升高)。在终末期心力衰竭患者(EF<50%)中,sACE2活性进一步升高,而在CRT后心力衰竭改善(逆向重构)时,sACE2活性降低。患病群体中血清血管紧张素转换酶(ACE)浓度较低,但与超声心动图参数没有很强的相关性。
可溶性ACE2活性似乎是心力衰竭以及可能即将发生心力衰竭的高血压中的生物标志物。我们的数据表明,sACE2参与了高血压和HF的发病机制。