Evidence map›Paper›PMID 38226800›Full record

ArticleBiomolecules & biomedicine2024

ELANE rs17223045C/T and rs3761007G/A variants: Protective factors against COVID-19.

José Manuel Fragoso, Gilberto Vargas-Alarcón, Ángel Emmanuel Martínez-Flores, Isela Montufar-Robles, Rosa Elda Barbosa-Cobos, Gustavo Rojas-Velasco, Julian Ramírez-Bello

Open access · diamondAbstract read
In one paragraph

Article in Biomolecules & biomedicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.8field-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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
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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

7 authors at 2 institutions in 1 country.

José Manuel FragosoLaboratorio de Biología Molecular, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico.
Gilberto Vargas-AlarcónDirección de Investigación, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico.
Ángel Emmanuel Martínez-FloresUnidad de Investigación, Hospital Juárez de México, Mexico City, Mexico.
Isela Montufar-RoblesUnidad de Investigación, Hospital Juárez de México, Mexico City, Mexico.
Rosa Elda Barbosa-CobosServicio de Reumatología, Hospital Juárez de México, Mexico City, Mexico.
Gustavo Rojas-VelascoUnidad de Cuidados Intensivos, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico.
Julian Ramírez-BelloSubdirección de Investigación Clínica, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico.
Instituto Nacional de Cardiología · MXHospital Juárez de México · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is responsible for causing coronavirus disease 2019 (COVID-19). The development and severity of this infectious disease is influenced by a combination of environmental and genetic factors. Angiotensin-converting enzyme 2 (ACE2) facilitates SARS-CoV-2 entry into human cells, with transmembrane serine protease 2 (TMPRSS2) playing a crucial role in S protein priming. Other proteases, such as cathepsin L and elastase, neutrophil-expressed (ELANE), have the capability to prime the S protein and contribute to SARS-CoV-2 infection. ELANE variants have not been previously examined in COVID-19 patients. We aimed to assess the association of single nucleotide variants (SNVs) within ELANE with COVID-19 and biochemical markers. The study included 319 SARS-CoV-2-infected patients and 288 controls. Genotyping of ELANE rs17216663C/T (Pro257Leu), rs17223045C/T (As1n30Asn), and rs3761007G/A was conducted using a 5'-nuclease allelic discrimination assay (TaqMan assay). Our findings indicate that ELANE rs17223045C/T (C vs T: odds ratio [OR] 0.08, P = 0.005, and CC vs CT: OR 0.08, P = 0.005) and rs3761007G/A (G vs A: OR 0.38, P = 0.009, and GG vs GA: OR 0.40, P = 0.008) confer protection against COVID-19. However, these variants were not associated with biochemical markers. In conclusion, our data suggests that ELANE rs17223045C/T and rs3761007G/A SNVs may play a protective role against COVID-19.

Indexed as

COVID-19Leukocyte ElastasePolymorphism, Single NucleotideAdultAgedAngiotensin-Converting Enzyme 2Case-Control StudiesFemaleHumansMaleMiddle AgedProtective FactorsSARS-CoV-2Angiotensin-Converting Enzyme 2ELANE protein, humanLeukocyte Elastase

Identifiers

PMID38226800
PMCPMC11088890
OpenAlexW4390882839

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.