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Plasma Angiotensin Converting Enzyme 2 (ACE2) Activity in Healthy Controls and Patients with Cardiovascular Risk Factors and/or Disease.
Lim, Hui Yin; Patel, Sheila K; Huang, Ping; Tacey, Mark; Choy, Kay Weng; Wang, Julie; Donnan, Geoffrey; Nandurkar, Harshal H; Ho, Prahlad; Burrell, Louise M.
  • Lim HY; Northern Pathology Victoria, Northern Health, Epping, Melbourne, VIC 3076, Australia.
  • Patel SK; Department of Medicine, Northern Health, University of Melbourne, Epping, Melbourne, VIC 3076, Australia.
  • Huang P; Department of Medicine, Austin Health, University of Melbourne, Heidelberg, Melbourne, VIC 3084, Australia.
  • Tacey M; Australian Centre for Blood Diseases, Monash University, Melbourne VIC 3004, Australia.
  • Choy KW; Department of Medicine, Austin Health, University of Melbourne, Heidelberg, Melbourne, VIC 3084, Australia.
  • Wang J; Department of Medicine, Austin Health, University of Melbourne, Heidelberg, Melbourne, VIC 3084, Australia.
  • Donnan G; The Northern Hospital, Epping, VIC 3076, Australia.
  • Nandurkar HH; Department of Medicine & Radiology, University of Melbourne, Parkville, VIC 3052, Australia.
  • Ho P; Northern Pathology Victoria, Northern Health, Epping, Melbourne, VIC 3076, Australia.
  • Burrell LM; Northern Pathology Victoria, Northern Health, Epping, Melbourne, VIC 3076, Australia.
J Pers Med ; 12(9)2022 Sep 13.
Article in English | MEDLINE | ID: covidwho-2033039
ABSTRACT
Angiotensin 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.
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Full text: Available Collection: International databases Database: MEDLINE Type of study: Observational study / Prognostic study / Randomized controlled trials Language: English Year: 2022 Document Type: Article Affiliation country: Jpm12091495

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Observational study / Prognostic study / Randomized controlled trials Language: English Year: 2022 Document Type: Article Affiliation country: Jpm12091495