Evidence map›Paper›PMID 37147677›Full record

ArticleRespiratory research2023

IL-6 and cfDNA monitoring throughout COVID-19 hospitalization are accurate markers of its outcomes.

Salvador Bello, Ana Belén Lasierra, Lucía López-Vergara, Cristina de Diego, Laura Torralba, Pablo Ruiz de Gopegui, Raquel Lahoz, Claudia Abadía, Javier Godino, Alberto Cebollada and 4 more

Open access · goldAbstract read
In one paragraph

Article in Respiratory research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
4.7field-weighted citation impact, top 4% 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

12 citing papers in PubMed, 24 citations in OpenAlex.

  1. Cell-Free DNA-Based Theranostics for Inflammatory Disorders.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  2. Article
  3. Article
  4. Observational
  5. [Examination of the Thermal Stability and Swallowing Safety of a Self-Developed Enteral Nutrition Thickening Agent].Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition · 2024
    Article
  6. Article
  7. Hypobaric hypoxia modulated structural characteristics of circulating cell-free DNA in high-altitude pulmonary edema.American journal of physiology. Lung cellular and molecular physiology · 2024
    Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
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

14 authors at 5 institutions in 1 country.

Salvador BelloDepartment of Pulmonary Medicine, Miguel Servet University Hospital, CIBERES, Instituto de Investigación Sanitaria (ISS) Aragón, Avenida Isabel La Católica 1-9, 50009, Zaragoza, Spain. sbello@salud.aragon.es.
Ana Belén LasierraDepartment of Biochemistry, San Jorge Hospital, Huesca, Spain.
Lucía López-VergaraDepartment of Pulmonary Medicine, Miguel Servet University Hospital, CIBERES, Instituto de Investigación Sanitaria (ISS) Aragón, Avenida Isabel La Católica 1-9, 50009, Zaragoza, Spain.
Cristina de DiegoDepartment of Pulmonary Medicine, Miguel Servet University Hospital, CIBERES, Instituto de Investigación Sanitaria (ISS) Aragón, Avenida Isabel La Católica 1-9, 50009, Zaragoza, Spain.
Laura TorralbaDepartment of Pulmonary Medicine, Miguel Servet University Hospital, CIBERES, Instituto de Investigación Sanitaria (ISS) Aragón, Avenida Isabel La Católica 1-9, 50009, Zaragoza, Spain.
Pablo Ruiz de GopeguiIntensive Care Unit, Miguel Servet University Hospital, Zaragoza, Spain.
Raquel LahozDepartment of Biochemistry, Miguel Servet University Hospital, Zaragoza, Spain.
Claudia AbadíaDepartment of Biochemistry, Miguel Servet University Hospital, Zaragoza, Spain.
Javier GodinoDepartment of Cytometry and Cell Separation, Aragon Institute of Health Sciences (IACS), Zaragoza, Spain.
Alberto CebolladaBiocomputing Technical Scientific Service, Aragon Institute of Health Sciences (IACS), Zaragoza, Spain.
Beatriz JimenoDepartment of Cytometry and Cell Separation, Aragon Institute of Health Sciences (IACS), Zaragoza, Spain.
Carlota BelloDepartment of Radiology, Hospital Clínico Lozano Blesa, Zaragoza, Spain.
Antonio TejadaIntensive Care Unit, Miguel Servet University Hospital, Zaragoza, Spain.
Antoni TorresServei de Pneumologia, Hospital Clinic, Universitat de Barcelona, IDIBAPS, ICREA, CIBERESUCICOVID, Barcelona, Spain.
Hospital Universitario Miguel Servet · ESInstituto de Investigación Sanitaria Aragón · ESCentro de Investigación Biomédica en Red de Enfermedades Respiratorias · ESHospital Clínico Universitario Lozano Blesa · ESHospital General San Jorge · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSevere COVID-19 entails a dysregulated immune response, most likely inflammation related to a lack of virus control. A better understanding of immune toxicity, immunosuppression balance, and COVID-19 assessments could help determine whether different clinical presentations are driven by specific types of immune responses. The progression of the immune response and tissular damage could predict outcomes and may help in the management of patients.

methodsWe collected 201 serum samples from 93 hospitalised patients classified as moderately, severely, and critically ill. We differentiated the viral, early inflammatory, and late inflammatory phases and included 72 patients with 180 samples in separate stages for longitudinal study and 55 controls. We studied selected cytokines, P-selectin, and the tissue damage markers lactate dehydrogenase (LDH) and cell-free DNA (cfDNA).

resultsTNF-α, IL-6, IL-8, and G-CSF were associated with severity and mortality, but only IL-6 increased since admission in the critical patients and non-survivors, correlating with damage markers. The lack of a significant decrease in IL-6 levels in the critical patients and non-survivors in the early inflammatory phase (a decreased presence in the other patients) suggests that these patients did not achieve viral control on days 10-16. For all patients, lactate dehydrogenase and cfDNA levels increased with severity, and cfDNA levels increased in the non-survivors from the first sample (p = 0.002) to the late inflammatory phase (p = 0.031). In the multivariate study, cfDNA was an independent risk factor for mortality and ICU admission.

conclusionsThe distinct progression of IL-6 levels in the course of the disease, especially on days 10-16, was a good marker of progression to critical status and mortality and could guide the start of IL-6 blockade. cfDNA was an accurate marker of severity and mortality from admission and throughout COVID-19 progression.

Indexed as

Cell-Free Nucleic AcidsCOVID-19BiomarkersHospitalizationHumansInterleukin-6Lactate DehydrogenasesLongitudinal StudiesBiomarkersCell-Free Nucleic AcidsInterleukin-6Lactate DehydrogenasesCell free DNACOVID-19IL-6ImmunityLongitudinal studyMortalitySeverity

Identifiers

PMID37147677
PMCPMC10161166
OpenAlexW4372335313

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.