Evidence map›Paper›PMID 30579356›Full record

ArticleLipids in health and disease2018

Association between MEG3/miR-181b polymorphisms and risk of ischemic stroke.

Xuemei Han, Zhaoshi Zheng, Chunhui Wang, Libo Wang

Open access · goldAbstract read
In one paragraph

Article in Lipids in health and disease, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.4field-weighted citation impact, top 22% 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

24 citing papers in PubMed, 39 citations in OpenAlex.

  1. Interaction of miR-181b andBioMed research international · 2020
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  4. Expert opinion on therapeutic targets · 2024
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  15. lncRNA MEG3 Downregulation Relieves Intracerebral Hemorrhage by Inhibiting Oxidative Stress and Inflammation in an miR-181b-Dependent Manner.Medical science monitor : international medical journal of experimental and clinical research · 2021
    Article
  16. Review
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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

4 authors at 3 institutions in 1 country.

Xuemei HanNo. 1 Department of Neurology, China-Japan Union Hospital of Jilin University, Changchun, Jilin, 130031, People's Republic of China.
Zhaoshi ZhengNo. 1 Department of Neurology, China-Japan Union Hospital of Jilin University, Changchun, Jilin, 130031, People's Republic of China.
Chunhui WangDepartment of Neurosurgery, the Hospital of Jilin Province, Changchun, Jilin, 130031, People's Republic of China.
Libo WangNo. 1 Department of Neurology, China-Japan Union Hospital of Jilin University, Changchun, Jilin, 130031, People's Republic of China. 935583975@qq.com.
Jilin University · CNPeople 's Hospital of Jilin Province · CNUnion Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRecent evidence suggests that long non-coding RNAs (lncRNAs) are key regulators in the pathological process of ischemic stroke (IS). Maternally expressed gene 3 (MEG3) was observed to be up-regulated in IS, acting as a competing endogenous RNA for miR-181b to regulate ischemic brain injury. The purpose of this study was to evaluate the association of tagSNPs in MEG3 (i.e., rs7158663 and rs4081134) and miR-181b rs322931 with IS risk.

methodsGenomic DNA was extracted from blood samples of 509 patients with IS and 668 healthy controls. Genotyping of MEG3 rs7158663, rs4081134, and miR-181b rs322931 was performed by TaqMan assay. The transcriptional activity was measured using the Dual-Luciferase Reporter Assay kit.

resultsSingle-site analysis revealed a significantly higher risk of IS being associated with miR-181b rs322931 CT and CT/TT genotypes (CT vs. CC: adjusted OR = 1.48, 95% CI: 1.13-1.95, P = 0.005; CT/TT vs. CC: adjusted OR = 1.52, 95% CI: 1.17-1.97, P = 0.002). Combined analyses revealed that combined genotypes (rs7158663 GG + rs322931 CT/TT and rs7158663 AG/AA + rs322931 CT/TT) increased IS risk compared to genotypes of rs7158663 GG + rs322931 CC. Stratification analyses showed that patients carrying miR-181b rs322931 CT/TT genotypes had higher levels of low-density lipoprotein cholesterol (LDL_C) (P = 0.01). Moreover, results from logistic regression analysis showed that rs322931 CT/TT genotypes were risk factors besides hypertension, total cholesterol, triglyceride, and LDL_C. Further dual-luciferase reporter assay showed that the rs322931 T allele had lower levels of luciferase activity than the rs322931 C allele.

conclusionThese findings indicate that miR-181b rs322931 may singly or jointly contribute to the risk of IS.

Indexed as

Brain IschemiaGenetic Predisposition to DiseasePolymorphism, Single NucleotideAgedAsian PeopleFemaleGene Expression RegulationHumansMaleMicroRNAsMiddle AgedRNA, Long NoncodingStrokeMEG3 non-coding RNA, humanMicroRNAsMIrn181 microRNA, humanRNA, Long NoncodingIschemic strokeLong non-coding RNAsMaternally expressed gene 3miR-181Polymorphism

Identifiers

PMID30579356
PMCPMC6303848
OpenAlexW2905724303

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.