Evidence map›Paper›PMID 31656272›Full record

ArticleJournal of atherosclerosis and thrombosis2020

Long Non-Coding RNA MEG3 Promotes Apoptosis of Vascular Cells and is Associated with Poor Prognosis in Ischemic Stroke.

Meiping Wang, Wenjuan Chen, Yu Geng, Chenghua Xu, Xiaoxiao Tao, Yi Zhang

Open access · diamondAbstract read
In one paragraph

Article in Journal of atherosclerosis and thrombosis, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.3field-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

18 citing papers in PubMed, 33 citations in OpenAlex.

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  11. Epigenetic mechanisms and potential therapeutic targets in stroke.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2022
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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

6 authors at 2 institutions in 1 country.

Meiping WangDepartment of Neurology, Zhejiang Provincial People's Hospital, People's Hospital of Hangzhou Medical.
Wenjuan ChenDepartment of Neurology, Zhejiang Provincial People's Hospital, People's Hospital of Hangzhou Medical.
Yu GengDepartment of Neurology, Zhejiang Provincial People's Hospital, People's Hospital of Hangzhou Medical.
Chenghua XuDepartment of Neurology, Taizhou First People's Hospital, Huangyan Hospital of Wenzhou Medical University.
Xiaoxiao TaoDepartment of Neurology, Taizhou First People's Hospital, Huangyan Hospital of Wenzhou Medical University.
Yi ZhangDepartment of Neurology, Taizhou First People's Hospital, Huangyan Hospital of Wenzhou Medical University.
Wenzhou Medical University · CNZhejiang Provincial People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimThis study focused on the expression pattern of long non-coding RNA maternally expressed gene 3 (MEG3) and its value in ischemic stroke (IS).

methodsThe expression pattern and the roles of MEG3 in the development of IS were explored in mice IS model and human brain microvascular endothelial cells (hBMECs). A case-control study, including 215 IS patients and 153 controls, was also conducted to investigate its prognostic value.

resultsIn vivo study showed that MEG3 increased significantly in the IS group (P=0.004), and its level remained stable within 3 to 48h after the onset of IS. Besides, the survival time of the mouse in the high MEG3 group was significantly lower than that in the low MEG3 group (P=0.042). In vitro study showed that oxygen-glucose deprivation (OGD) treatment significantly up-regulated expressions of MEG3, Bax, and cleaved caspase-3, and further promoted apoptosis of hBMECs, while si-MEG3 blocked these effects. A human study showed that MEG3 increased markedly within 48h of IS onset and was positively associated with the National Institutes of Health Stroke Scale (r=0.347, P<0.001), modified Rankin Scale (r=0.385, P<0.001), high-sensitivity C-reactive protein (r=0.221, P=0.002) level, and infarct volume (r=0.201, P=0.006). Overall survival analysis showed that patients with higher MEG3 expression within 48h had a relatively poor prognosis (P<0.001). Meanwhile, multivariate analysis revealed that MEG3 was an independent prognostic marker for unfavorable functional outcome and death in IS patients.

conclusionsThis study suggested that MEG3 might be considered as an intervention point and potential prognostic indicator for IS.

Indexed as

Ischemic StrokeRNA, Long NoncodingAgedAnimalsApoptosisApoptosis Regulatory ProteinsCase-Control StudiesChinaDisease Models, AnimalFemaleFunctional StatusGene Expression ProfilingGene Expression RegulationHumansMalePredictive Value of TestsApoptosis Regulatory ProteinsMEG3 non-coding RNA, humanMEG3 non-coding RNA, mouseRNA, Long NoncodingIschemic strokeLong non-coding RNAMaternally expressed gene 3Prognosis

Identifiers

PMID31656272
PMCPMC7406404
OpenAlexW2982271392

What OpenQuestion holds

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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.