Evidence map›Paper›PMID 37176577›Full record

ArticleJournal of clinical medicine2023

sST2 and Heart Failure-Clinical Utility and Prognosis.

Magdalena Dudek, Marta Kałużna-Oleksy, Jacek Migaj, Filip Sawczak, Helena Krysztofiak, Maciej Lesiak, Ewa Straburzyńska-Migaj

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07029230 (Biomarker in Congenital Cardiac Surgery - sST2 Marker in Heart Failure in Congenital Heart Disease After Surgery Research and Translational Study), which is not on this map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
5.3field-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.

NCT07029230 recruitingnot on this mapstarted 2025, after this paper: background citation

Biomarker in Congenital Cardiac Surgery - sST2 Marker in Heart Failure in Congenital Heart Disease After Surgery Research and Translational Study

TypeobservationalSponsorMartin SchweigerRan2025 to 2029Enrolled225ConditionsCongenital Heart Surgery, Congenital Heart Disease in Children, Fontan Physiology
3 · Its place in the literature

Who cites it

19 citing papers in PubMed, 32 citations in OpenAlex.

  1. Review
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  11. Is soluble ST2 an useful biomarker for early diagnosis of coronary atherosclerosis?Hypertension research : official journal of the Japanese Society of Hypertension · 2025
    Article
  12. Article
  13. Article
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  15. Review
  16. Review
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  19. Soluble ST2 in Heart Failure: A Clinical Role beyond B-Type Natriuretic Peptide.Journal of cardiovascular development and disease · 2023
    Review
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 2 institutions in 1 country.

Magdalena Dudek1st Department of Cardiology, Poznań University of Medical Sciences, 61-848 Poznań, Poland.ORCID 0000-0001-6550-6182
Marta Kałużna-Oleksy1st Department of Cardiology, Poznań University of Medical Sciences, 61-848 Poznań, Poland.ORCID 0000-0003-4048-6247
Jacek Migaj1st Department of Cardiology, Poznań University of Medical Sciences, 61-848 Poznań, Poland.
Filip Sawczak1st Department of Cardiology, Poznań University of Medical Sciences, 61-848 Poznań, Poland.ORCID 0000-0003-3449-8751
Helena KrysztofiakDepartment of Cardiology, University Hospital in Opole, 45-401 Opole, Poland.
Maciej Lesiak1st Department of Cardiology, Poznań University of Medical Sciences, 61-848 Poznań, Poland.
Ewa Straburzyńska-Migaj1st Department of Cardiology, Poznań University of Medical Sciences, 61-848 Poznań, Poland.
Poznan University of Medical Sciences · PLUniversity of Opole · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

New parameters and markers are constantly being sought to help better assess patients with heart failure (HF). ST2 protein has gained interest as a potential biomarker in cardiovascular disease. It is known that the IL-33/ST2L system belongs to the cardioprotective pathway, which prevents the fibrosis, hypertrophy, and apoptosis of cardiomyocytes and also inhibits the inflammatory response. Soluble ST2 (sST2) is involved in the immune response and secreted in response to the mechanical overload of the myocardium, thus providing information on the processes of myocardial remodeling and fibrosis. A total of 110 hospitalized patients diagnosed with heart failure with reduced ejection fraction (HFrEF) were included in the study. Clinical and biochemical parameters were studied. During the follow-up, 30.9% patients died and 57.3% patients reached the composite endpoint. Using ROC curves, the reference cut-off point for sST2 was determined to be 45.818 pg/mL for all-cause deaths. Significantly higher concentrations of inflammatory parameters and natriuretic peptides were found in the group of patients with higher sST2 concentrations. sST2 protein is an independent risk factor for all-cause deaths of patients with HFrEF.

Indexed as

biomarkerheart failureHFrEFsST2

Identifiers

PMID37176577
PMCPMC10179304
OpenAlexW4367182379

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.