Evidence map›Paper›PMID 36082632›Full record

ArticleTherapeutic advances in respiratory disease

The prognostic importance of the angiotensin II/angiotensin-(1-7) ratio in patients with SARS-CoV-2 infection.

Luis M Amezcua-Guerra, Leonardo Del Valle, Héctor González-Pacheco, Rashidi Springall, Ricardo Márquez-Velasco, Felipe Massó, Malinalli Brianza-Padilla, Daniel Manzur-Sandoval, Julieta González-Flores, Carlos García-Ávila and 12 more

Open access · goldAbstract read
In one paragraph

Article in Therapeutic advances in respiratory disease. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.8field-weighted citation impact, top 13% 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

8 citing papers in PubMed, 18 citations in OpenAlex.

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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

22 authors at 1 institution in 1 country.

Luis M Amezcua-GuerraImmunology Department, Ignacio Chávez National Institute of Cardiology, Mexico City, Mexico.
Leonardo Del VallePharmacology Department, Ignacio Chávez National Institute of Cardiology, Mexico City, Mexico.
Héctor González-PachecoCoronary Care Unit, Ignacio Chávez National Institute of Cardiology, Mexico City, Mexico.
Rashidi SpringallImmunology Department, Ignacio Chávez National Institute of Cardiology, Mexico City, Mexico.
Ricardo Márquez-VelascoImmunology Department, Ignacio Chávez National Institute of Cardiology, Mexico City, Mexico.
Felipe MassóTranslational Medicine Lab UNAM-INC Unit, Ignacio Chávez National Institute of Cardiology, Mexico City, Mexico.
Malinalli Brianza-PadillaImmunology Department, Ignacio Chávez National Institute of Cardiology, Mexico City, Mexico.
Daniel Manzur-SandovalIntensive Care Unit, Ignacio Chávez National Institute of Cardiology, Mexico City, Mexico.
Julieta González-FloresImmunology Department, Ignacio Chávez National Institute of Cardiology, Mexico City, Mexico.
Carlos García-ÁvilaImmunology Department, Ignacio Chávez National Institute of Cardiology, Mexico City, Mexico.
Yaneli Juárez-VicuñaImmunology Department, Ignacio Chávez National Institute of Cardiology, Mexico City, Mexico.
Fausto Sánchez-MuñozImmunology Department, Ignacio Chávez National Institute of Cardiology, Mexico City, Mexico.
Martha A Ballinas-VerdugoImmunology Department, Ignacio Chávez National Institute of Cardiology, Mexico City, Mexico.
Edna Basilio-GálvezImmunology Department, Ignacio Chávez National Institute of Cardiology, Mexico City, Mexico.
Araceli Paez-ArenasTranslational Medicine Lab UNAM-INC Unit, Ignacio Chávez National Institute of Cardiology, Mexico City, Mexico.
Mauricio Castillo-SalazarImmunology Department, Ignacio Chávez National Institute of Cardiology, Mexico City, Mexico.
Sergio Cásares-AlvaradoImmunology Department, Ignacio Chávez National Institute of Cardiology, Mexico City, Mexico.
Adrián Hernández-DiazcouderImmunology Department, Ignacio Chávez National Institute of Cardiology, Mexico City, Mexico.
José L Sánchez-GloriaImmunology Department, Ignacio Chávez National Institute of Cardiology, Mexico City, Mexico.
Claudia Tavera-AlonsoCore Lab, Ignacio Chávez National Institute of Cardiology, Mexico City, Mexico.
Rodrigo Gopar-NietoCoronary Care Unit, Ignacio Chávez National Institute of Cardiology, Mexico City, Mexico.ORCID 0000-0002-4865-4869
Julio SandovalImmunology Department, Ignacio Chávez National Institute of Cardiology, Juan Badiano # 1, Colonia Sección XVI Tlalpan, México City 14080, México.
Instituto Nacional de Cardiología · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInformation about angiotensin II (Ang II), angiotensin-converting enzyme 2 (ACE2), and Ang-(1-7) levels in patients with COVID-19 is scarce.

objectiveTo characterize the Ang II-ACE2-Ang-(1-7) axis in patients with SARS-CoV-2 infection to understand its role in pathogenesis and prognosis.

methodsPatients greater than 18 years diagnosed with COVID-19, based on clinical findings and positive RT-PCR test, who required hospitalization and treatment were included. We compared Ang II, aldosterone, Ang-(1-7), and Ang-(1-9) concentrations and ACE2 concentration and activity between COVID-19 patients and historic controls. We compared baseline demographics, laboratory results (enzyme, peptide, and inflammatory marker levels), and outcome (patients who survived

resultsSerum from 74 patients [age: 58 (48-67.2) years; 68% men] with moderate (20%) or severe (80%) COVID-19 were analyzed. During 13 (10-21) days of hospitalization, 25 patients died from COVID-19 and 49 patients survived. Compared with controls, Ang II concentration was higher and Ang-(1-7) concentration was lower, despite significantly higher ACE2 activity in patients. Ang II concentration was higher and Ang-(1-7) concentration was lower in patients who died. The Ang II/Ang-(1-7) ratio was significantly higher in patients who died. In multivariate analysis, Ang II/Ang-(1-7) ratio greater than 3.45 (OR = 5.87) and lymphocyte count ⩽0.65 × 10

conclusionIn patients with severe SARS-CoV-2 infection, imbalance in the Ang II-ACE2-Ang-(1-7) axis may reflect deleterious effects of Ang II and may indicate a worse outcome.

Indexed as

Angiotensin-Converting Enzyme 2Angiotensin IAngiotensin IICOVID-19Angiotensin-Converting Enzyme InhibitorsFemaleHumansMaleMiddle AgedPeptide FragmentsPeptidyl-Dipeptidase APrognosisSARS-CoV-2Angiotensin-Converting Enzyme 2Angiotensin-Converting Enzyme InhibitorsAngiotensin Iangiotensin I (1-7)Angiotensin IIPeptide FragmentsPeptidyl-Dipeptidase Aangiotensin-(1-7)angiotensin-converting enzyme 2angiotensin IICOVID-19SARS-CoV-2

Identifiers

PMID36082632
PMCPMC9465579
OpenAlexW4295088792

What OpenQuestion holds

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LicenceCC BY-NC
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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.