Evidence map›Paper›PMID 40656787›Full record

ArticleCardiovascular diagnosis and therapy2025

The value of miRNA-29b in the diagnosis of myocardial infarction and the evaluation of cardiac function after myocardial infarction.

Xiaoxi Wang, Xuexin Liu, Weihua Shao, Yawei Duan, Huiqing Hou

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Article in Cardiovascular diagnosis and therapy, 2025. 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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5 · Who and what money

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5 authors.

Xiaoxi WangDepartment of Physical Examination Center, Hebei General Hospital, Shijiazhuang, China.
Xuexin LiuDepartment of Physical Examination Center, Hebei General Hospital, Shijiazhuang, China.
Weihua ShaoDepartment of Geriatric Cardiology, Hebei General Hospital, Shijiazhuang, China.
Yawei DuanDepartment of Cardiovascular Medicine, Hebei General Hospital, Shijiazhuang, China.
Huiqing HouDepartment of Audit Office, Hebei General Hospital, Shijiazhuang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: miRNA-29b affects angiogenesis and cardiac fibrosis, processes relevant to the pathophysiology of myocardial infarction (MI). This study aimed to investigate the accuracy of miRNA-29b in diagnosing acute myocardial infarction (AMI) and its association with postinfarction cardiac function. Methods: A total of 106 patients with AMI admitted to the Department of Cardiology of Hebei General Hospital between January 2023 and July 2024 were prospectively enrolled within 24 hours of symptom onset. Indicators including circulating miRNA-29b levels [detected via real-time quantitative polymerase chain reaction (RT-qPCR)], myocardial enzymes, vascular endothelial growth factor (VEGF), and tumor necrosis factor-α (TNF-α) were assessed at baseline. Cardiac function was assessed by echocardiography. Left ventricular ejection fraction (LVEF), left ventricular fractional shortening (LVFS), left ventricular end-diastolic diameter (LVEDd), left ventricular end-systolic diameter (LVEDs), and left ventricular posterior wall thickness at end-diastole (LVPWd) and end-systole (LVPWs) were also measured. Based on echocardiography, patients with AMI (n=106) were divided into an abnormal cardiac function (ACF) group (LVEF <50%; n=50) or a normal cardiac function (NCF) group (LVEF ≥50%; n=56). Thirty healthy participants were selected as the control group. Variables were compared with independent samples t-tests. Correlation and receiver operating characteristic (ROC) curve analyses were also conducted. Results: There was no significant differences in baseline demographic or clinical characteristics between the AMI and control groups; however, the control group, compared with the AMI group, had lower levels of low-density lipoprotein cholesterol (2.72±0.58 Conclusions: Blood miRNA-29b is lower in patients with AMI, particularly in those with impaired cardiac function. miRNA-29b demonstrates potential value in the diagnosis of AMI and the assessment of postinfarction cardiac function.

Indexed as

cardiac function assessmentmiRNA-29bmyocardial infarction (MI)

Identifiers

PMID40656787
PMCPMC12246988

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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 OpenQuestion graph.