Evidence map›Paper›PMID 34933965›Full record

Observational studyOpen heart2021

Soluble ST2 concentrations associate with in-hospital mortality and need for mechanical ventilation in unselected patients with COVID-19.

Torbjorn Omland, Christian Prebensen, Christine Jonassen, My Svensson, Jan Erik Berdal, Ingebjørg Seljeflot, Peder Langeland Myhre

Registry-linked trialOpen access · goldAbstract readObservational Study
In one paragraph

Observational study in Open heart, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04314232 (Changes in Organ Specific Biomarkers, Virus Expression and Prognosis of Covid-19), which is not on this map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.1field-weighted citation impact, top 23% 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.

NCT04314232 unknown statusnot on this map

Changes in Organ Specific Biomarkers, Virus Expression and Prognosis of Covid-19

TypeobservationalSponsorUniversity Hospital, AkershusRan2020 to 2021Enrolled200ConditionsCOVID, Coronavirus Infection
3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 20 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. A biomarker for bacteremia in pregnant women with acute pyelonephritis: soluble suppressor of tumorigenicity 2 or sST2.The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians · 2023
    Article
  7. Article
  8. 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

7 authors at 3 institutions in 1 country.

Torbjorn OmlandDepartment of Cardiology, Akershus University Hospital, Lorenskog, Norway.
Christian PrebensenInstitute of Clinical Medicine, Faculty of Medicine, University of Oslo, Oslo, Norway.
Christine JonassenCenter for Laboratory Medicine, Østfold Hospital Trust, Grålum, Norway.
My SvenssonInstitute of Clinical Medicine, Faculty of Medicine, University of Oslo, Oslo, Norway.
Jan Erik BerdalInstitute of Clinical Medicine, Faculty of Medicine, University of Oslo, Oslo, Norway.
Ingebjørg SeljeflotInstitute of Clinical Medicine, Faculty of Medicine, University of Oslo, Oslo, Norway.
Peder Langeland MyhreDepartment of Cardiology, Akershus University Hospital, Lorenskog, Norway p.l.myhre@medisin.uio.no.ORCID 0000-0002-5871-1804
University of Oslo · NOOslo University Hospital · NOØstfold Hospital Trust · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveSoluble ST2 (sST2) reflects inflammation, endothelial dysfunction and myocardial fibrosis, is produced in the lungs and is an established biomarker in heart failure. We sought to determine the role of sST2 in COVID-19 by assessing pathophysiological correlates and its association to in-hospital outcomes.

methodsWe enrolled 123 consecutive, hospitalised patients with COVID-19 in the prospective, observational COVID-19 MECH study. Biobank samples were collected at baseline, day 3 and day 9. The key exposure variable was sST2, and the outcome was ICU treatment with mechanical ventilation or in-hospital death.

resultsConcentrations of sST2 at baseline was median 48 (IQR 37-67) ng/mL, and 74% had elevated concentrations (>37.9 ng/mL). Higher baseline sST2 concentrations were associated with older age, male sex, white race, smoking, diabetes, hypertension and chronic kidney disease. Baseline sST2 also associated with the presence of SARS-CoV-2 viraemia, lower oxygen saturation, higher respiratory rate and increasing concentrations of biomarkers reflecting inflammation, thrombosis and cardiovascular disease. During the hospitalisation, 8 (7%) patients died and 27 (22%) survivors received intensive care unit (ICU) treatment. Baseline sST2 concentrations demonstrated a graded association with disease severity (median, IQR): medical ward 43 (36-59) ng/mL; ICU 67 (39-104) ng/mL and non-survivors 107 (72-116) ng/mL (p<0.001 for all comparisons). These associations persisted at day 3 and day 9 .

conclusionssST2 concentrations associate with SARS-CoV-2 viraemia, hypoxaemia and concentrations of inflammatory and cardiovascular biomarkers. There was a robust association between baseline sST2 and disease severity that was independent of, and superior to, established risk factors. sST2 reflects key pathophysiology and may be a promising biomarker in COVID-19. TRIAL REGISTRATION NUMBER: NCT04314232.

Indexed as

COVID-19HypoxiaViremiaAgedBiomarkersComorbidityCorrelation of DataFemaleHospital MortalityHumansIntensive Care UnitsInterleukin-1 Receptor-Like 1 ProteinMaleMiddle AgedNorwayPrognosisBiomarkersIL1RL1 protein, humanInterleukin-1 Receptor-Like 1 ProteinbiomarkersCOVID-19risk factors

Identifiers

PMID34933965
PMCPMC8692780
OpenAlexW4200573343

What Socratic holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

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.