Evidence map›Paper›PMID 41847510›Full record

ArticleFrontiers in cardiovascular medicine2026

Prognostic utility of Wnt/β-catenin signaling pathway biomarkers in predicting outcomes of patients with ST-segment elevation myocardial infarction.

Lei Wang, Chengmin Tao, Lingfei Yang

Abstract read
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Article in Frontiers in cardiovascular medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Lei WangDepartment of Cardiovascular Medicine, The Second Affiliated Hospital of Wannan Medical College, Wuhu, Anhui, China.
Chengmin TaoDepartment of Cardiovascular Medicine, Wuhu First People's Hospital, Wuhu, Anhui, China.
Lingfei YangDepartment of Cardiovascular Medicine, The Second Affiliated Hospital of Wannan Medical College, Wuhu, Anhui, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: To investigate the expression profiles of Wnt/β-catenin signaling pathway-related biomarkers in patients with ST-segment elevation myocardial infarction (STEMI) and to evaluate their predictive value for major adverse cardiovascular events (MACE). Methods: A total of 200 STEMI patients admitted to the emergency department between August 2021 and August 2024 were enrolled. Peripheral venous blood samples were collected immediately before emergency percutaneous coronary intervention (PCI) and serum levels of Wnt1, β-catenin, Wnt5a, secreted frizzled-related protein 5 (SFRP5), and Dickkopf-related protein 1 (DKK1) were measured using enzyme-linked immunosorbent assay. Based on the occurrence of MACE during hospitalization and within 1-year follow-up, patients were categorized into the MACE group ( Results: Serum levels of Wnt1, β-catenin, Wnt5a, and DKK1 were elevated, whereas SFRP5 was markedly reduced in the MACE group. Patients with high serum levels of Wnt1, β-catenin, Wnt5a, or DKK1 had significantly higher MACE incidence rates, while those with high SFRP5 levels had a lower incidence. β-catenin, DKK1, and cardiac troponin I (cTnI) were identified as independent risk factors for MACE in STEMI patients. The combined prediction model of β-catenin and DKK1 (AUC = 0.946; 95% CI = 0.910-0.981) showed superior predictive performance compared with single biomarkers. Conclusion: The combined detection of β-catenin and DKK1 may serve as a potential biomarker for risk stratification in STEMI patients.

Indexed as

biomarkermajor adverse cardiovascular eventsprognosisST-segment elevation myocardial infarctionWnt/β-catenin signaling

Identifiers

PMID41847510
PMCPMC12989540

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