Evidence map›Paper›PMID 37685970›Full record

ArticleInternational journal of molecular sciences2023

Serum High-Mobility Group Box 1 and Heme Oxygenase-1 as Biomarkers in COVID-19 Patients at Hospital Admission.

Ilijana Grigorov, Snežana Pejić, Ana Todorović, Dunja Drakulić, Filip Veljković, Jadranka Miletić Vukajlović, Katarina Bobić, Ivan Soldatović, Siniša Đurašević, Nebojša Jasnić and 4 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 30% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. 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

14 authors at 1 institution in 1 country.

Ilijana GrigorovInstitute for Biological Research "Siniša Stanković"-National Institute of the Republic of Serbia, University of Belgrade, 11000 Belgrade, Serbia.ORCID 0000-0001-9540-4961
Snežana PejićVinča Institute of Nuclear Sciences-National Institute of the Republic of Serbia, University of Belgrade, 11000 Belgrade, Serbia.ORCID 0000-0003-4573-2371
Ana TodorovićVinča Institute of Nuclear Sciences-National Institute of the Republic of Serbia, University of Belgrade, 11000 Belgrade, Serbia.ORCID 0000-0002-2074-1637
Dunja DrakulićVinča Institute of Nuclear Sciences-National Institute of the Republic of Serbia, University of Belgrade, 11000 Belgrade, Serbia.
Filip VeljkovićVinča Institute of Nuclear Sciences-National Institute of the Republic of Serbia, University of Belgrade, 11000 Belgrade, Serbia.
Jadranka Miletić VukajlovićVinča Institute of Nuclear Sciences-National Institute of the Republic of Serbia, University of Belgrade, 11000 Belgrade, Serbia.
Katarina BobićVinča Institute of Nuclear Sciences-National Institute of the Republic of Serbia, University of Belgrade, 11000 Belgrade, Serbia.ORCID 0000-0001-9575-0960
Ivan SoldatovićInstitute of Medical Statistics and Informatic, Faculty of Medicine, University of Belgrade, 11000 Belgrade, Serbia.ORCID 0000-0003-4893-1683
Siniša ĐuraševićFaculty of Biology, University of Belgrade, 11000 Belgrade, Serbia.ORCID 0000-0003-4406-8376
Nebojša JasnićFaculty of Biology, University of Belgrade, 11000 Belgrade, Serbia.ORCID 0000-0003-0333-333X
Sanja StankovićCenter for Medical Biochemistry, University Clinical Center of Serbia, 11000 Belgrade, Serbia.ORCID 0000-0003-0890-535X
Sofija GlumacInstitute of Pathology, School of Medicine, University of Belgrade, 11000 Belgrade, Serbia.
Violeta Mihailović-VučinićInstitute of Pathology, School of Medicine, University of Belgrade, 11000 Belgrade, Serbia.
Branislava MilenkovićInstitute of Pathology, School of Medicine, University of Belgrade, 11000 Belgrade, Serbia.ORCID 0000-0002-0767-6869
University of Belgrade · RS

Funding

Science Fund of the Republic of Serbia 7551587
6 · The paper itself

Abstract

The careful monitoring of patients with mild/moderate COVID-19 is of particular importance because of the rapid progression of complications associated with COVID-19. For prognostic reasons and for the economic management of health care resources, additional biomarkers need to be identified, and their monitoring can conceivably be performed in the early stages of the disease. In this retrospective cross-sectional study, we found that serum concentrations of high-mobility group box 1 (HMGB1) and heme oxygenase-1 (HO-1), at the time of hospital admission, could be useful biomarkers for COVID-19 management. The study included 160 randomly selected recovered patients with mild to moderate COVID-19 on admission. Compared with healthy controls, serum HMGB1 and HO-1 levels increased by 487.6 pg/mL versus 43.1 pg/mL and 1497.7 pg/mL versus 756.1 pg/mL, respectively. Serum HO-1 correlated significantly with serum HMGB1, oxidative stress parameters (malondialdehyde (MDA), the phosphatidylcholine/lysophosphatidylcholine ratio (PC/LPC), the ratio of reduced and oxidative glutathione (GSH/GSSG)), and anti-inflammatory acute phase proteins (ferritin, haptoglobin). Increased heme catabolism/hemolysis were not detected. We hypothesize that the increase in HO-1 in the early phase of COVID-19 disease is likely to have a survival benefit by providing protection against oxidative stress and inflammation, whereas the level of HMGB1 increase reflects the activity of the innate immune system and represents levels within which the disease can be kept under control.

Indexed as

COVID-19HMGB1 ProteinBiomarkersCross-Sectional StudiesGlutathioneHeme Oxygenase-1HospitalsHumansRetrospective StudiesBiomarkersGlutathioneHeme Oxygenase-1HMGB1 ProteinCOVID-19heme oxygenase-1 (HO-1)high-mobility group box 1(HMGB1)predictive biomarkerSARS-CoV-2

Identifiers

PMID37685970
PMCPMC10488018
OpenAlexW4386137828

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.