Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/17837
Title: Elevated plasma angiotensin converting enzyme 2 activity is an independent predictor of major adverse cardiac events in patients with obstructive coronary artery disease.
Austin Authors: Ramchand, Jay ;Patel, Sheila K ;Srivastava, Piyush M ;Farouque, Omar ;Burrell, Louise M 
Affiliation: Medicine (University of Melbourne)
Cardiology
Issue Date: 13-Jun-2018
Date: 2018-06-13
Publication information: PLoS One 2018; 13(6): e0198144
Abstract: Angiotensin converting enzyme 2 (ACE2) is an endogenous regulator of the renin angiotensin system. Increased circulating ACE2 predicts adverse outcomes in patients with heart failure (HF), but it is unknown if elevated plasma ACE2 activity predicts major adverse cardiovascular events (MACE) in patients with obstructive coronary artery disease (CAD). We prospectively recruited patients with obstructive CAD (defined as ≥50% stenosis of the left main coronary artery and/or ≥70% stenosis in ≥ 1 other major epicardial vessel on invasive coronary angiography) and measured plasma ACE2 activity. Patients were followed up to determine if circulating ACE2 activity levels predicted the primary endpoint of MACE (cardiovascular mortality, HF or myocardial infarction). We recruited 79 patients with obstructive coronary artery disease. The median (IQR) plasma ACE2 activity was 29.3 pmol/ml/min [21.2-41.2]. Over a median follow up of 10.5 years [9.6-10.8years], MACE occurred in 46% of patients (36 events). On Kaplan-Meier analysis, above-median plasma ACE2 activity was associated with MACE (log-rank test, p = 0.035) and HF hospitalisation (p = 0.01). After Cox multivariable adjustment, log ACE2 activity remained an independent predictor of MACE (hazard ratio (HR) 2.4, 95% confidence interval (CI) 1.24-4.72, p = 0.009) and HF hospitalisation (HR: 4.03, 95% CI: 1.42-11.5, p = 0.009). Plasma ACE2 activity independently increased the hazard of adverse long-term cardiovascular outcomes in patients with obstructive CAD.
URI: https://ahro.austin.org.au/austinjspui/handle/1/17837
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0198144
ORCID: 0000-0003-1863-7539
0000-0002-0626-1899
Journal: PLoS One
PubMed URL: 29897923
Type: Journal Article
Appears in Collections:Journal articles

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