Emerging markers in cardiovascular disease: Where does angiotensin-converting enzyme 2 fit in?

• Published in: Clinical and experimental pharmacology & physiology Vol. 40; no. 8; pp. 551 - 559
• Main Authors: Patel, Sheila K, Velkoska, Elena, Burrell, Louise M
• Format: Journal Article
• Language: English
• Published: Australia Blackwell Publishing Ltd 01.08.2013; Wiley Subscription Services, Inc
• Subjects: angiotensin-converting enzyme 2; Biomarkers; cardiovas-cular disease; Cardiovascular diseases; Cardiovascular Diseases - genetics; Cardiovascular Diseases - metabolism; coronary artery disease; Gene Expression Regulation, Enzymologic; Health risks; heart failure; Humans; Kidney transplantation; Peptidyl-Dipeptidase A - genetics; Peptidyl-Dipeptidase A - metabolism; renin-angiotensin system; Renin-Angiotensin System - physiology; Risk Factors; Sex Factors; coronary artery disease; heart failure; angiotensin-converting enzyme 2; renin-angiotensin system; cardiovas-cular disease
• ISSN: 0305-1870; 1440-1681; 1440-1681
• DOI: 10.1111/1440-1681.12069

Summary The renin–angiotensin system plays a major role in the pathophysiology of cardiovascular disease (CVD). The enzyme angiotensin‐converting enzyme (ACE) converts angiotensin (Ang) I into the vasoconstrictor AngII and was thought, until recently, to be the main effector of the system. The enzyme ACE2, discovered in 2000, can counterbalance the effects of ACE through degradation of AngII and generation of Ang‐(1–7). Angiotensin‐converting enzyme 2 is abundantly expressed in the heart and localized to the endothelial cells of coronary vessels and smooth muscle cells. Its catalytically active ectodomain undergoes shedding, resulting in ACE2 in the circulation. There are 10 studies to date that have measured circulating ACE2 activity in humans, including in healthy subjects and those with heart failure, Type 1 diabetes, implantable cardioverter/defibrillator, elderly subjects undergoing emergency orthopaedic surgery and kidney transplant patients. The results suggest that circulating ACE2 activity may be a marker of CVD, with low levels in healthy individuals and increased levels in those with cardiovascular risk factors or disease. Whether increased plasma ACE2 activity reflects increased synthesis from tissue ACE2 mRNA or increased shedding of tissue ACE2 remains to be determined. Angiotensin‐converting enzyme 2 is located on the X‐chromosome and circulating ACE2 levels are higher in men than in women. Large clinical studies in CVD are needed to more precisely clarify the role of ACE2 as a biomarker of CVD, determine the prognostic significance of circulating ACE2 activity and assess whether the measurement of ACE2 will improve CVD risk prediction.