Evidence map›Paper›PMID 36593047›Full record

ArticleIn vivo (Athens, Greece)

Angiotensin Converting Enzyme 1 Polymorphisms and Lipid Profile in Mexican Patients With COVID-19.

Evelyn Romero Mateos, Paola Berenice Zarate, Fernando Bastida Gonzalez, Maria Jose Perez-Mendez, Eduardo Dávila-Gonzalez, Aaron Garduno-Gutierrez, Rosalva Sotelo-Salas, Ceballos-Macias Jose Juan, Sosa-Corales Horacio, Lucio-Monter Pascual Francisco and 1 more

Open access · diamondAbstract read
In one paragraph

Article in In vivo (Athens, Greece). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.2field-weighted citation impact, top 54% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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

11 authors at 4 institutions in 1 country.

Evelyn Romero MateosDepartment of Postgraduate Studies, Medical School, National Polytechnic Institute, Mexico City, Mexico.
Paola Berenice ZarateDepartment of Postgraduate Studies, Medical School, National Polytechnic Institute, Mexico City, Mexico.
Fernando Bastida GonzalezMolecular Biology Laboratory, Public Health Laboratory of Mexico State, Toluca, Mexico.
Maria Jose Perez-MendezDepartment of Postgraduate Studies, Medical School, National Polytechnic Institute, Mexico City, Mexico.
Eduardo Dávila-GonzalezMolecular Biology Laboratory, Public Health Laboratory of Mexico State, Toluca, Mexico.
Aaron Garduno-GutierrezDepartment of Epidemiology, Tlalnepantla Health Jurisdiction, Tlalnepantla, Mexico.
Rosalva Sotelo-SalasDepartment of Epidemiology, Tlalnepantla Health Jurisdiction, Tlalnepantla, Mexico.
Ceballos-Macias Jose JuanPunta Medica Hospital, Tlalnepantla, Mexico.
Sosa-Corales HoracioCentral Military Hospital, Mexico City, Mexico.
Lucio-Monter Pascual FranciscoCentral Military Hospital, Mexico City, Mexico.
Cleva VillanuevaDepartment of Postgraduate Studies, Medical School, National Polytechnic Institute, Mexico City, Mexico; gvillanueval@ipn.mx.
Instituto Politécnico Nacional · MXHospital Central Militar · MXHospital Médica Sur · MXTecnológico Nacional de México · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimRenin-angiotensin system (RAS) is present in a diverse type of cells and plays an important role in lung physiology and pathophysiology. Angiotensin converting enzymes (ACE) are part of the RAS system. There are still controversies about the association of I/D polymorphisms of ACE1 with COVID-19 severity. The goal of the study was to determine whether there is an association of the I/D polymorphism with severity of COVID-19 in Mexican patients. PATIENTS AND

methodsThe study included voluntary participants: 53 healthy individuals negative to RT-PCR COVID-19 (control), and 165 patients positive to COVID-19. Severity was defined by the need of hospitalization, invasive ventilation, shock, or multiple organ failure. The patient group consisted of 28 asymptomatic, 82 with mild, and 55 with severe COVID-19. I/D polymorphism was determined by PCR. Rutinary laboratory tests were performed in all the participants.

resultsDD polymorphism was significantly associated with severe COVID-19, independently of comorbidities, or any other variable. Receiver operator characteristic curves demonstrated association of low total cholesterol, low high-density lipoproteins, and high c-reactive protein with severity of COVID-19.

conclusionThe DD polymorphism was associated with the course of the infection and severity of COVID-19 in a sample of Mexican patients.

Indexed as

COVID-19HumansLipidsNorth American PeoplePeptidyl-Dipeptidase APolymorphism, GeneticRenin-Angiotensin SystemACE protein, humanLipidsPeptidyl-Dipeptidase AACE-1asymptomaticCOVID-19I/D polymorphismlipid profilesevere

Identifiers

PMID36593047
PMCPMC9843789
OpenAlexW4313475209

What Socratic holds

Textmetadata
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 Socratic graph.