Evidence map›Paper›PMID 32090249›Full record

ArticleBioscience reports2020

Promoter polymorphisms in the lncRNA-MIAT gene associated with acute myocardial infarction in Chinese Han population: a case-control study.

Ruchao Ma, Xiaohui He, Xiaoyun Zhu, Shuchao Pang, Bo Yan

Open access · goldAbstract read
In one paragraph

Article in Bioscience reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-weighted citation impact, top 37% 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

8 citing papers in PubMed, 13 citations in OpenAlex.

  1. Association ofInternational journal of medical sciences · 2026
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  2. Puzzling out the role ofNon-coding RNA research · 2024
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  8. The Long Non-coding Road to Atherosclerosis.Current atherosclerosis reports · 2020
    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

5 authors at 3 institutions in 1 country.

Ruchao MaShandong University Cheeloo College of Medicine, Jinan, Shandong 250012, China.
Xiaohui HeShandong University Cheeloo College of Medicine, Jinan, Shandong 250012, China.
Xiaoyun ZhuDivision of Gastroenterology and Hepatology, Gansu Provincial Hospital, Lanzhou, Gansu 730030, China.
Shuchao PangThe Center for Molecular Genetics of Cardiovascular Disease, Affiliated Hospital of Jining Medical University, Jining Medical University, Jining, Shandong 272029, China.
Bo YanThe Center for Molecular Genetics of Cardiovascular Disease, Affiliated Hospital of Jining Medical University, Jining Medical University, Jining, Shandong 272029, China.
Affiliated Hospital of Jining Medical University · CNShandong University · CNGansu Provincial Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCoronary atherosclerotic disease (CAD) is one of the greatest causes of death and disability around the world, and has emerged as a major public health problem. Acute myocardial infarction (AMI) is the most serious type of CAD. Myocardial infarction (MI) association transcript (MIAT) has demonstrated that it plays an important role in AMI. PURPOSE: To investigate the association between MIAT promoter polymorphisms and AMI in Chinese Han population.

methodsA total of 212 AMI patients and 218 healthy controls were recruited. The long non-coding RNA (lncRNA)-MIAT promoter polymorphisms (single nucleotide polymorphisms (SNPs)) were obtained using polymerase chain reaction (PCR) and sequencing techniques. Chi-square test was used to analyze the allele and genotype frequencies of each SNP in two groups. Logistic regression analysis was used to analyze the association of each SNP with AMI. Linkage disequilibrium (LD) and haplotype analysis were performed using SHEsis software. A JASPAR database search predicts transcription factors transition of linked polymorphism in MIAT promoter.

resultsTen SNPs were found, including rs56371714, rs55892869, rs151057042, rs2157598, rs150465374, rs5761664, rs8142890, rs5752375, rs9608515 and rs1055293700, whereas rs1055293700 was found only in the control group. Single and logistic regression analysis showed that there was a significant correlation between rs5752375 and rs9608515 polymorphisms and AMI, while other sites had no relationship with AMI. These MI association polymorphisms may change the binding sites with transcription factor.

conclusionsThe polymorphisms of lncRNA-MIAT promoter rs5752375 and rs9608515 were significantly associated with AMI in Chinese Han population. This result would be of clinical importance for the early diagnosis of AMI.

Indexed as

Polymorphism, Single NucleotidePromoter Regions, GeneticAdultAsian PeopleCase-Control StudiesChinaFemaleGenetic Association StudiesGenetic Predisposition to DiseaseHaplotypesHumansLinkage DisequilibriumMaleMiddle AgedMyocardial InfarctionPhenotypeMiat long non-coding RNARNA, Long NoncodingAcute myocardial infarctionCoronary atherosclerotic diseaseMyocardial infarction associated transcriptPolymorphism

Identifiers

PMID32090249
PMCPMC7040461
OpenAlexW3005769584

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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 OpenQuestion graph.