Evidence mapPaperPMID 37697243Full record

ArticleBMC cardiovascular disorders2023

The role of miR1 and miR133a in new-onset atrial fibrillation after acute myocardial infarction.

Qingyi Zeng, Wei Li, Zhenghua Luo, Haiyan Zhou, Zhonggang Duan, Xin Lin Xiong

Open access · goldAbstract read
In one paragraph

Article in BMC cardiovascular disorders, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.9field-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.

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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. International journal of molecular sciences · 2025
    Article
  3. 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

6 authors at 3 institutions in 1 country.

Qingyi ZengGuizhou Medical University, 9 Beijing Road, Guiyang, 550000, Guizhou, China.
Wei LiGuizhou Medical University, 9 Beijing Road, Guiyang, 550000, Guizhou, China. liwei249188@sina.com.
Zhenghua LuoGuizhou Provincial People's Hospital, 83 Zhongshan East Road, Guiyang, 55000, Guizhou, China.
Haiyan ZhouGuizhou Medical University, 9 Beijing Road, Guiyang, 550000, Guizhou, China.
Zhonggang DuanGuizhou Medical University, 9 Beijing Road, Guiyang, 550000, Guizhou, China.
Xin Lin XiongGuizhou Medical University, 9 Beijing Road, Guiyang, 550000, Guizhou, China.
Guiyang Medical University · CNAffiliated Hospital of Guizhou Medical University · CNGuizhou Provincial People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe development of new-onset atrial fibrillation (NOAF) after acute myocardial infarction (AMI) is a clinical complication that requires a better understanding of the causative risk factors. This study aimed to explore the risk factors and the expression and function of miR-1 and miR-133a in new atrial fibrillation after AMI.

methodsWe collected clinical data from 172 patients with AMI treated with emergency percutaneous coronary intervention (PCI) between October 2021 and October 2022. Independent predictors of NOAF were determined using binary logistic univariate and multivariate regression analyses. The predictive value of NOAF was assessed using the area under the receiver operating characteristic (ROC) curve for related risk factors. In total, 172 venous blood samples were collected preoperatively and on the first day postoperatively; the expression levels of miR-1 and miR-133a were determined using the polymerase chain reaction. The clinical significance of miR-1 and miR-133a expression levels was determined by Spearman correlation analysis.

resultsThe Glasgow prognostic score, left atrial diameter, and infarct area were significant independent risk factors for NOAF after AMI. We observed that the expression levels of miR-1 and miR-133a were significantly higher in the NOAF group than in the non-NOAF group. On postoperative day 1, strong associations were found between miR-133a expression levels and the neutrophil ratio and between miR-1 expression levels and an increased left atrial diameter.

conclusionsOur findings indicate that the mechanism of NOAF after AMI may include an inflammatory response associated with an increased miR-1-related mechanism. Conversely, miR-133a could play a protective role in this clinical condition.

Indexed as

Atrial AppendageAtrial FibrillationMicroRNAsMyocardial InfarctionPercutaneous Coronary InterventionHumansMicroRNAsMIRN133 microRNA, humanMIRN1 microRNA, humanAcute myocardial infarctionBlood sedimentationGlasgow prognostic scoreInflammationLeft atrial diametermiR1miR133aNew-onset atrial fibrillation

Identifiers

PMID37697243
PMCPMC10496401
OpenAlexW4386599751

What Socratic holds

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LicenceCC BY
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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.