Evidence map›Paper›PMID 32557866›Full record

ArticleJournal of clinical laboratory analysis2020

Association of genetic variants in lncRNA GAS5/miR-21/mTOR axis with risk and prognosis of coronary artery disease among a Chinese population.

Hu Li, Yingxue Liu, Jinyan Huang, Yu Liu, Yufeng Zhu

Abstract read
In one paragraph

Article in Journal of clinical laboratory analysis, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Article
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  4. Influence of rsHealth science reports · 2025
    Article
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  8. The effect of MicroRNAs variants on idiopathic recurrent pregnancy loss.Journal of assisted reproduction and genetics · 2023
    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

5 authors.

Hu LiDepartment of Cardiology, The First Naval Hospital of Southern Theater Command, Zhanjiang City, China.ORCID https://orcid.org/0000-0002-5926-4591
Yingxue LiuDepartment of Outpatient, The First Naval Hospital of Southern Theater Command, Zhanjiang City, China.
Jinyan HuangDepartment of Cardiology, The First Naval Hospital of Southern Theater Command, Zhanjiang City, China.
Yu LiuDepartment of Cardiology, The First Naval Hospital of Southern Theater Command, Zhanjiang City, China.
Yufeng ZhuDepartment of Cardiology, The First Naval Hospital of Southern Theater Command, Zhanjiang City, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAllowing for the significance of single nucleotide polymorphisms (SNPs) in reflecting disease risk, this investigation attempted to uncover whether SNPs situated in lncRNA GAS5/miR-21/mTOR axis were associated with risk and prognosis of coronary heart disease (CHD) among a Chinese Han population.

methodsAltogether 436 patients with CHD were recruited as cases, and meanwhile, 471 healthy volunteers were included into the control group. Besides, SNPs of GAS5/MIR-21/mTOR axis were genotyped utilizing mass spectrometry. Chi-square test was applied to figure out SNPs that were strongly associated with CHD risk and prognosis, and combined effects of SNPs and environmental parameters on CHD risk were evaluated through multifactor dimensionality reduction (MDR) model.

resultsSingle nucleotide polymorphisms of GAS5 (ie, rs2067079 and rs6790), MIR-21 (ie, rs1292037), and mTOR (rs2295080, rs2536, and rs1034528) were associated with susceptibility to CHD, and also Gensini score change of patients with CHD (P < .05). MDR results further demonstrated that rs2067079 and rs2536 were strongly interactive in elevating CHD risk (P < .05), while smoking, rs6790 and rs2295080 showed powerful reciprocity in predicting Gensini score change of patients with CHD (P < .05).

conclusionSingle nucleotide polymorphisms of lncRNA GAS5/miR-21/mTOR axis might interact with smoking to regulate CHD risk, which was conducive to diagnosis and prognostic anticipation of CHD.

Indexed as

Genetic Association StudiesGenetic Predisposition to DiseaseAsian PeopleCase-Control StudiesCoronary Artery DiseaseEnvironmental ExposureFemaleHaploidyHumansMaleMicroRNAsPolymorphism, Single NucleotidePrognosisRisk FactorsRNA, Long NoncodingTOR Serine-Threonine KinasesGAS5 long non-coding RNA, humanMicroRNAsMIRN21 microRNA, humanMTOR protein, humanRNA, Long NoncodingTOR Serine-Threonine Kinasescoronary heart diseaselncRNA GAS5miR-21mTORprognosissingle nucleotide polymorphism

Identifiers

PMID32557866
PMCPMC7595889

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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.