Evidence map›Paper›PMID 42495606›Full record

ArticleFrontiers in immunology2026

High levels of miR-146a-5p in COVID-19 patients are associated with

Gloria Pérez-Rubio, Ricardo A Herrera-Sicairos, Leslie Chavez-Galan, Samuel Campista-León, Luz Isela Peinado-Guevara, Ivette Buendia-Roldan, Lucero A Ramon-Luing, Ingrid Fricke-Galindo, Brandon Bautista-Becerril, Ramcés Falfán-Valencia

Abstract read
In one paragraph

Article in Frontiers in immunology, 2026. 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
–field-weighted citation impact
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.

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

10 authors.

Gloria Pérez-RubioPneumogenomics Laboratory, Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas, Mexico, Mexico.
Ricardo A Herrera-SicairosPneumogenomics Laboratory, Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas, Mexico, Mexico.
Leslie Chavez-GalanLaboratory of Integrative Immunology, Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas, Mexico, Mexico.
Samuel Campista-LeónLaboratory of Microbiology and Applied Biology, Faculty of Biology, Universidad Autónoma de Sinaloa, Culiacán Rosales, Sinaloa, Mexico.
Luz Isela Peinado-GuevaraLaboratory of Microbiology and Applied Biology, Faculty of Biology, Universidad Autónoma de Sinaloa, Culiacán Rosales, Sinaloa, Mexico.
Ivette Buendia-RoldanTranslational Research Laboratory on Aging and Pulmonary Fibrosis, Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas, Mexico, Mexico.
Lucero A Ramon-LuingLaboratory of Integrative Immunology, Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas, Mexico, Mexico.
Ingrid Fricke-GalindoPneumogenomics Laboratory, Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas, Mexico, Mexico.
Brandon Bautista-BecerrilPneumogenomics Laboratory, Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas, Mexico, Mexico.
Ramcés Falfán-ValenciaPneumogenomics Laboratory, Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas, Mexico, Mexico.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Bacterial coinfections in COVID-19 patients present significant clinical challenges, particularly in severe cases. Previous studies have highlighted the role of microRNAs (miRNAs) in regulating immune responses, with miR-146a-5p and miR-21-5p implicated in inflammation and immune modulation. This study examines the effect of bacterial coinfections on the expression levels of these miRNAs in patients with severe COVID-19. Methods: We conducted a cohort study involving Mexican mestizo patients ≥18 years hospitalized with severe COVID-19, confirmed via PCR testing. Patients were categorized based on the presence or absence of bacterial coinfection, determined through bronchial aspirate or sputum culture. Blood samples were collected at admission and after 15 days of hospitalization to measure the relative expression levels of miR-146a-5p and miR-21-5p. Additionally, an Results: Patients with bacterial coinfection were older (43 vs. 41 years, p = 0.046) and had a higher BMI than those without (29.40 vs. 27.51 kg/m2, p = 0.006). The PaO Conclusions: Patients with COVID-19 and bacterial coinfection exhibit worse clinical indicators and increased disease severity, demonstrated by older age, higher BMI, severe hypoxemia, greater need for IMV, and increased mortality. Patients with COVID-19 and coinfection with

Indexed as

CoinfectionCOVID-19Klebsiella InfectionsMicroRNAsAdultFemaleHumansMaleMexicoMiddle AgedSARS-CoV-2MicroRNAsMIRN146 microRNA, humanBacterial coinfectionCOVID-19IMVKlebsiellamiR-146a-5p

Identifiers

PMID42495606
PMCPMC13391917

What Socratic holds

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LicenceCC BY
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Registered trials

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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.