Evidence map›Paper›PMID 37715121›Full record

ArticleBMC infectious diseases2023

Differential expression of biomarkers in saliva related to SARS-CoV-2 infection in patients with mild, moderate and severe COVID-19.

Lázaro Verdiguel-Fernández, Rene Arredondo-Hernández, Jesús Andrés Mejía-Estrada, Adolfo Ortiz, Antonio Verdugo-Rodríguez, Patricia Orduña, Samuel Ponce de León-Rosales, Juan José Calva, Yolanda López-Vidal

Open access · goldAbstract read
In one paragraph

Article in BMC infectious diseases, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

7 citing papers in PubMed, 7 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

9 authors at 3 institutions in 2 countries.

Lázaro Verdiguel-FernándezDepartamento de Microbiología Y Parasitología, Programa de Inmunología Molecular Microbiana, Facultad de Medicina, UNAM, CDMX, México.
Rene Arredondo-HernándezLaboratorio de Microbioma, División de Investigación, Facultad de Medicina, UNAM, CDMX, México.
Jesús Andrés Mejía-EstradaDepartamento de Microbiología Y Parasitología, Programa de Inmunología Molecular Microbiana, Facultad de Medicina, UNAM, CDMX, México.
Adolfo OrtizDepartamento de Microbiología E Inmunología, Unidad de Bioseguridad de Brucella, Facultad de Medicina Veterinaria Y Zootecnia, Universidad Nacional Autónoma de México, CDMX, México.
Antonio Verdugo-RodríguezDepartamento de Microbiología E Inmunología, Laboratorio de Microbiología Molecular, Facultad de Medicina Veterinaria Y Zootecnia, Universidad Nacional Autónoma de México, CDMX, México.
Patricia OrduñaLaboratorio de Microbioma, División de Investigación, Facultad de Medicina, UNAM, CDMX, México.
Samuel Ponce de León-RosalesPrograma Universitario de Investigación en Salud, Universidad Nacional Autónoma de México, CDMX, México.
Juan José CalvaDepartamento de Infectología, Instituto Nacional de Ciencias Médicas y Nutrición "Salvador Zubirán", CDMX, México. juanjcalva@gmail.com.
Yolanda López-VidalDepartamento de Microbiología Y Parasitología, Programa de Inmunología Molecular Microbiana, Facultad de Medicina, UNAM, CDMX, México. lvidal@unam.mx.
Universidad Nacional Autónoma de México · MXInstituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán · MXLaboratory of Molecular Genetics · PL

Funding

CONACyT for the postdoctoral scholarship granted to CVU 391838 CVU 391838General Directorate of Academic Staff Affairs- Support Program for Research Projects in Technological Innovation DGAPA-PAPIIT IV200321, IT 202020
6 · The paper itself

Abstract

backgroundSevere COVID-19 is a disease characterized by profound dysregulation of the innate immune system. There is a need to identify highly reliable prognostic biomarkers that can be rapidly assessed in body fluids for early identification of patients at higher risk for hospitalization and/or death. This study aimed to assess whether differential gene expression of immune response molecules and cellular enzymes, detected in saliva samples of COVID-19 patients, occurs according to disease severity staging.

methodsIn this cross-sectional study, subjects with a COVID-19 diagnosis were classified as having mild, moderate, or severe disease based on clinical features. Transcripts of genes encoding 6 biomarkers, IL-1β, IL-6, IL-10, C-reactive protein, IDO1 and ACE2, were measured by RT‒qPCR in saliva samples of patients and COVID-19-free individuals.

resultsThe gene expression levels of all 6 biomarkers in saliva were significantly increased in severe disease patients compared to mild/moderate disease patients and healthy controls. A significant strong inverse relationship between oxemia and the level of expression of the 6 biomarkers (Spearman's correlation coefficient between -0.692 and -0.757; p < 0.001) was found.

conclusionsBiomarker gene expression determined in saliva samples still needs to be validated as a potentially valuable predictor of severe clinical outcomes early at the onset of COVID-19 symptoms.

Indexed as

COVID-19SalivaBiomarkersCOVID-19 TestingCross-Sectional StudiesHumansSARS-CoV-2BiomarkersACE2BiomarkersCOVID-19CytokinesIDO1SalivaSeverity

Identifiers

PMID37715121
PMCPMC10502992
OpenAlexW4386780086

What OpenQuestion holds

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LicenceCC BY
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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.