Evidence map›Paper›PMID 33469835›Full record

ArticleGeroScience2021

Level of the SARS-CoV-2 receptor ACE2 activity is highly elevated in old-aged patients with aortic stenosis: implications for ACE2 as a biomarker for the severity of COVID-19.

Miklós Fagyas, Attila Kertész, Ivetta Mányiné Siket, Viktor Bánhegyi, Bertalan Kracskó, Andrea Szegedi, Miklós Szokol, Gusztáv Vajda, Ildikó Rácz, Hajnalka Gulyás and 6 more

Open access · hybridAbstract read
In one paragraph

Article in GeroScience, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
4.4field-weighted citation impact, top 5% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 30 citations in OpenAlex.

  1. SARS-CoV-2 cell entry beyond the ACE2 receptor.Molecular biology reports · 2022
    Pooled it
  2. Article
  3. Article
  4. Article
  5. ACE2, ACE, DPPIV, PREP and CAT L enzymatic activities in COVID-19: imbalance of ACE2/ACE ratio and potential RAAS dysregulation in severe cases.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2023
    Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Circulating ACE2 activity predicts mortality and disease severity in hospitalized COVID-19 patients.International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases · 2022
    Article
  11. Article
  12. Article
  13. Towards Personalized Therapy of Aortic Stenosis.Journal of personalized medicine · 2021
    Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. 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

16 authors at 1 institution in 1 country.

Miklós Fagyas *Division of Clinical Physiology, Department of Cardiology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Attila Kertész *Department of Cardiology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Ivetta Mányiné SiketDivision of Clinical Physiology, Department of Cardiology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Viktor BánhegyiDivision of Clinical Physiology, Department of Cardiology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Bertalan KracskóDepartment of Cardiology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Andrea SzegediDepartment of Cardiology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Miklós SzokolDepartment of Cardiology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Gusztáv VajdaDepartment of Cardiology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Ildikó RáczDepartment of Cardiology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Hajnalka GulyásDivision of Clinical Physiology, Department of Cardiology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Noémi SzkibákDepartment of Cardiology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Vivienn RáczDepartment of Cardiology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Zoltán CsanádiDepartment of Cardiology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Zoltán PappDivision of Clinical Physiology, Department of Cardiology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Attila Tóth *Division of Clinical Physiology, Department of Cardiology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary. atitoth@med.unideb.hu.ORCID http://orcid.org/0000-0001-6503-3653
Sándor Sipka *Department of Cardiology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
University of Debrecen · HU

Funding

European Regional Development Fund GINOP-2.3.2-15-2016-00043European Regional Development Fund GINOP-2.3.2-15-2016-00050European Social Fund EFOP-3.6.2-16-2017-00006National Research, Development and Innovation Fund of Hungary FK 128809National Research, Development and Innovation Fund of Hungary K 116940National Research, Development and Innovation Fund of Hungary K 132623Thematic Excellence Programme of the Ministry for Innovation and Technology in Hungary ED_18-1-2019-0028
6 · The paper itself

Abstract

Coronavirus disease 2019 (COVID-19) has a high mortality in elderly patients with pre-existing cardiovascular diseases. The cellular receptor of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the angiotensin-converting enzyme 2 (ACE2), thereby implicating a link between cardiovascular diseases and SARS-CoV-2 susceptibility. Aortic stenosis (AS) represents a chronic inflammatory state with severe cardiovascular complications in the elderly, a prime condition for COVID-19 mortality. The circulating ACE2 levels were measured in 111 patients with severe AS and compared to patients with hypertension and healthy individuals. About 4 times higher circulating ACE2 activity was found in patients with severe AS than in hypertensives or healthy individuals (88.3 ± 61.6., n = 111, 20.6 ± 13.4, n = 540, and 16.1 ± 7.4 mU/L, n = 46, respectively). Patients with severe AS were older than patients with hypertension (80 ± 6 years vs. 60 ± 15 years, P < 0.05). Serum ACE2 activity correlated negatively with the left ventricular ejection fraction, aortic root area, TAPSE, and positively with the right ventricular systolic pressure, cardiac diameters in patients with AS. In contrast, circulating ACE2 activity was independent of the blood pressure, peak flow velocity at the aortic root, kidney function (GFR), and inflammatory state (CRP). We found no effect of RAAS inhibitory drugs on the serum ACE2 activity in this group of patients. Our results illustrate circulating ACE2 as a potential interface between chronic inflammation, cardiovascular disease, and COVID-19 susceptibility. Elderly patients with AS have markedly elevated ACE2 levels together with altered left and right ventricular functions, which may pose higher risks during COVID-19. Our clinical data do not support a role for RAAS inhibitors in regulating circulating ACE2 levels.

Indexed as

Aortic Valve StenosisCOVID-19AgedAngiotensin-Converting Enzyme 2BiomarkersHumansMiddle AgedPeptidyl-Dipeptidase ARenin-Angiotensin SystemSARS-CoV-2Stroke VolumeVentricular Function, LeftAngiotensin-Converting Enzyme 2BiomarkersPeptidyl-Dipeptidase AACE2 activityAortic stenosisCardiovascular diseaseCoronavirus disease 2019 (COVID-19)SARS-CoV-2

Identifiers

PMID33469835
PMCPMC7815502
OpenAlexW3123045749

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.