Evidence map›Paper›PMID 39614185›Full record

ArticleBMC cardiovascular disorders2024

Soluble suppression of tumorigenicity 2 associated with microvascular obstruction in patients with ST-segment elevation myocardial infarction.

Xinjia Du, Jiahua Liu, Jingfang Zhou, Yanfei Ren, Nauman Gul, Lei Chen, Yuan Lu

Abstract read
In one paragraph

Article in BMC cardiovascular disorders, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Trial
  2. Evaluating the role of montelukast on doxorubicin-induced cardiotoxicity in breast cancer patients.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2025
    Trial
  3. Review
  4. Review
  5. 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

7 authors.

Xinjia Du *Department of Cardiology, The Affiliated Hospital of Xuzhou Medical University, Xuzhou, China.
Jiahua Liu *Department of Cardiology, The Affiliated Hospital of Xuzhou Medical University, Xuzhou, China.
Jingfang ZhouDepartment of Cardiology, The Affiliated Hospital of Xuzhou Medical University, Xuzhou, China.
Yanfei RenDepartment of Cardiology, The Affiliated Hospital of Xuzhou Medical University, Xuzhou, China.
Nauman GulDepartment of Cardiology, The Affiliated Hospital of Xuzhou Medical University, Xuzhou, China.
Lei ChenDepartment of Cardiology, Shanghai Tenth People's Hospital, Tongji University School of Medicine, Shanghai, China. drleichen@tongji.edu.cn.
Yuan LuDepartment of Cardiology, The Affiliated Hospital of Xuzhou Medical University, Xuzhou, China. drluyuan329@163.com.

Funding

China Postdoctoral Science Foundation funded project, the 68th batch of surface projects No. M681738Jiangsu Provincial Health Commission Medical Research Project No. M2021046
6 · The paper itself

Abstract

backgroundMicrovascular obstruction (MVO) develops in approximately 50% of patients with ST-segment elevation myocardial infarction (STEMI) after undergoing percutaneous coronary intervention (PCI). MVO is strongly linked to inflammation, myocardial fibrosis, and adverse clinical outcomes. Soluble suppression of tumorigenicity 2 (sST2) serves as a biomarker for inflammation and myocardial fibrosis. Yet, the correlation between sST2 and MVO in STEMI patients has not been fully elucidated. This study attempts to evaluate the association between sST2 levels and MVO in STEMI patients following pPCI.

methodsIn this retrospective study, 315 STEMI patients who underwent pPCI at the Affiliated Hospital of Xuzhou Medical University between June 2018 and August 2023 were included. Cardiac magnetic resonance imaging (CMR) was used to assess the characteristics of myocardial infarction and microvascular obstruction (MVO), while sST2 levels were measured upon admission.

resultsThe median time for completion of CMR after hospitalization was 5 (4, 6) days. Multivariate regression analysis showed that sST2 (OR 1.01, 95% CI 1.01-1.02, p < 0.001), peak high-sensitivity troponin T (OR 2.40, 95% CI 1.66-3.47, p < 0.001), peak high-C-reactive protein (OR 1.01, 95% CI 1.01-1.02, p < 0.001), left ventricular ejection fraction (OR 0.93, 95% CI 0.89- 0.98, p = 0.009) and age (OR 1.03, 95% CI 1.01- 1.05, p = 0.042)were independently associated with MVO.

conclusionsST2 is associated with MVO after pPCI in STEMI patients. Incorporating soluble ST2 (sST2) into the risk model for MVO leads to significant improvement.

Indexed as

BiomarkersCoronary CirculationInterleukin-1 Receptor-Like 1 ProteinMicrocirculationPercutaneous Coronary InterventionST Elevation Myocardial InfarctionAgedFemaleHumansMagnetic Resonance Imaging, CineMaleMiddle AgedPredictive Value of TestsRetrospective StudiesRisk AssessmentRisk FactorsBiomarkersIL1RL1 protein, humanInterleukin-1 Receptor-Like 1 ProteinCardiovascular magnetic resonanceMicrovascular obstructionMyocardial infarctionSoluble suppression of tumorigenicity 2

Identifiers

PMID39614185
PMCPMC11607795

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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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.