Evidence map›Paper›PMID 36143280›Full record

ArticleJournal of personalized medicine2022

Plasma Angiotensin Converting Enzyme 2 (ACE2) Activity in Healthy Controls and Patients with Cardiovascular Risk Factors and/or Disease.

Hui Yin Lim, Sheila K Patel, Ping Huang, Mark Tacey, Kay Weng Choy, Julie Wang, Geoffrey Donnan, Harshal H Nandurkar, Prahlad Ho, Louise M Burrell

Open access · goldAbstract read
In one paragraph

Article in Journal of personalized medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 33% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 6 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 4 institutions in 1 country.

Hui Yin LimNorthern Pathology Victoria, Northern Health, Epping, Melbourne, VIC 3076, Australia.ORCID 0000-0003-2455-3155
Sheila K PatelDepartment of Medicine, Austin Health, University of Melbourne, Heidelberg, Melbourne, VIC 3084, Australia.ORCID 0000-0002-0626-1899
Ping HuangDepartment of Medicine, Austin Health, University of Melbourne, Heidelberg, Melbourne, VIC 3084, Australia.
Mark TaceyThe Northern Hospital, Epping, VIC 3076, Australia.
Kay Weng ChoyNorthern Pathology Victoria, Northern Health, Epping, Melbourne, VIC 3076, Australia.
Julie WangNorthern Pathology Victoria, Northern Health, Epping, Melbourne, VIC 3076, Australia.ORCID 0000-0003-2857-6514
Geoffrey DonnanThe Melbourne Brain Centre, Royal Melbourne Hospital, University of Melbourne, Parkville, VIC 3052, Australia.
Harshal H NandurkarAustralian Centre for Blood Diseases, Monash University, Melbourne VIC 3004, Australia.
Prahlad HoNorthern Pathology Victoria, Northern Health, Epping, Melbourne, VIC 3076, Australia.
Louise M BurrellDepartment of Medicine, Austin Health, University of Melbourne, Heidelberg, Melbourne, VIC 3084, Australia.ORCID 0000-0003-1863-7539
The University of Melbourne · AUAustralian Centre for HIV and Hepatitis Virology Research · AUNorthern Health · AUThe Royal Melbourne Hospital · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

angiotensin converting enzyme 2cardiovascular diseasecoagulationrenin angiotensin system

Identifiers

PMID36143280
PMCPMC9501250
OpenAlexW4296004816

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.