Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/30939
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dc.contributor.authorLim, Hui Yin-
dc.contributor.authorPatel, Sheila K-
dc.contributor.authorHuang, Ping-
dc.contributor.authorTacey, Mark A-
dc.contributor.authorChoy, Kay Weng-
dc.contributor.authorWang, Julie-
dc.contributor.authorDonnan, Geoffrey A-
dc.contributor.authorNandurkar, Harshal H-
dc.contributor.authorHo, Prahlad-
dc.contributor.authorBurrell, Louise M-
dc.date2022-
dc.date.accessioned2022-09-30T06:17:44Z-
dc.date.available2022-09-30T06:17:44Z-
dc.date.issued2022-09-13-
dc.identifier.citationJournal of Personalized medicine 2022; 12(9)en
dc.identifier.issn2075-4426
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/30939-
dc.description.abstractAngiotensin converting enzyme 2 (ACE2) is an endogenous negative regulator of the renin-angiotensin system, a key factor in the development of cardiovascular disease (CVD). ACE2 is also used by SARS-CoV-2 for host cell entry. Given that COVID-19 is associated with hypercoagulability, it is timely to explore the potential relationship between plasma ACE2 activity and the coagulation profile. In this cross-sectional study, ACE2 activity and global coagulation assays (GCA) including thromboelastography, thrombin, and fibrin generation were measured in adult healthy controls (n = 123; mean age 41 ± 17 years; 35% male) and in patients with cardiovascular risk factors and/or disease (n = 258; mean age 65 ± 14 years; 55% male). ACE2 activity was significantly lower in controls compared to patients with cardiovascular risk factors and/or disease (median 0.10 (0.02, 3.33) vs. 5.99 (1.95, 10.37) pmol/mL/min, p < 0.001). Of the healthy controls, 48% had undetectable ACE2 activity. Controls with detectable ACE2 had lower maximum amplitude (p < 0.001). In patients with cardiovascular risk factors and/or disease, those in the 3rd tertile were older and male (p = 0.002), with a higher Framingham grade and increased number of cardiovascular risk factors (p < 0.001). In conclusion, plasma ACE2 activity is undetectable to very low in young healthy controls with minimal clinically relevant associations to GCA. Patients with cardiovascular risk factors and/or disease have increased plasma ACE2 activity, suggesting that it may be an important biomarker of endothelial dysfunction and atherosclerosis.en
dc.language.isoeng
dc.subjectangiotensin converting enzyme 2en
dc.subjectcardiovascular diseaseen
dc.subjectcoagulationen
dc.subjectrenin angiotensin systemen
dc.titlePlasma Angiotensin Converting Enzyme 2 (ACE2) Activity in Healthy Controls and Patients with Cardiovascular Risk Factors and/or Disease.en
dc.typeJournal Articleen
dc.identifier.journaltitleJournal of Personalized Medicineen
dc.identifier.affiliationThe Melbourne Brain Centre, Royal Melbourne Hospital, University of Melbourne, Parkville, VIC 3052,Australiaen
dc.identifier.affiliationNorthern Pathology Victoria, Northern Health, Epping, Melbourne, VIC 3076,Australiaen
dc.identifier.affiliationDepartment of Medicine, Northern Health, University of Melbourne, Epping, Melbourne, VIC 3076,Australiaen
dc.identifier.affiliationGeneral Medicineen
dc.identifier.affiliationAustralian Centre for Blood Diseases, Monash University, Melbourne VIC 3004,Australiaen
dc.identifier.affiliationThe Northern Hospital, Epping, VIC 3076,Australiaen
dc.identifier.affiliationDepartment of Medicine & Radiology, University of Melbourne, Parkville, VIC 3052,Australiaen
dc.identifier.doi10.3390/jpm12091495en
dc.type.contentTexten
dc.identifier.orcid0000-0003-2455-3155en
dc.identifier.orcid0000-0002-0626-1899en
dc.identifier.orcid0000-0003-2857-6514en
dc.identifier.orcid0000-0003-1863-7539en
dc.identifier.pubmedid36143280
local.name.researcherBurrell, Louise M
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.grantfulltextnone-
crisitem.author.deptMedicine (University of Melbourne)-
crisitem.author.deptRadiation Oncology-
crisitem.author.deptOlivia Newton-John Cancer Wellness and Research Centre-
crisitem.author.deptThe Florey Institute of Neuroscience and Mental Health-
crisitem.author.deptCardiology-
crisitem.author.deptGeneral Medicine-
crisitem.author.deptMedicine (University of Melbourne)-
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