Evidence map›Paper›PMID 31479479›Full record

ArticlePloS one2019

Analysis of potential roles of combinatorial microRNA regulation in occurrence of valvular heart disease with atrial fibrillation based on computational evidences.

Guangbin Wang, Nini Rao, Dingyun Liu, Hongxiu Jiang, Ke Liu, Feng Yang, Yangwei Chen, Keli Huang

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 50% 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

2 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Regulatory role of miRNAs in Wnt signaling pathway linked with cardiovascular diseases.Current research in pharmacology and drug discovery · 2022
    Article
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

8 authors at 1 institution in 1 country.

Guangbin WangCenter for Informational Biology, School of Life Science and Technology, University of Electronic Science and Technology of China, Chengdu, China.
Nini RaoCenter for Informational Biology, School of Life Science and Technology, University of Electronic Science and Technology of China, Chengdu, China.ORCID 0000-0001-7979-2917
Dingyun LiuCenter for Informational Biology, School of Life Science and Technology, University of Electronic Science and Technology of China, Chengdu, China.
Hongxiu JiangCenter for Informational Biology, School of Life Science and Technology, University of Electronic Science and Technology of China, Chengdu, China.
Ke LiuSubsidiary Hospital, University of Electronic Science and Technology of China, Chengdu, China.
Feng YangCenter for Informational Biology, School of Life Science and Technology, University of Electronic Science and Technology of China, Chengdu, China.
Yangwei ChenSchool of Life Science and Technology, University of Electronic Science and Technology of China, Chengdu, China.
Keli HuangSubsidiary Hospital, University of Electronic Science and Technology of China, Chengdu, China.
University of Electronic Science and Technology of China · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAtrial fibrillation (AF) is the most common arrhythmia. Patients with valvular heart disease (VHD) frequently have AF. Growing evidence demonstrates that a specifically altered pattern of microRNA (miRNA) expression is related to valvular heart disease with atrial fibrillation (AF-VHD) processes. However, the combinatorial regulation by multiple miRNAs in inducing AF-VHD remains largely unknown.

methodsThe work identified AF-VHD-specific miRNAs and their combinations through mapping miRNA expression profile into differential co-expression network. The expressions of some dysregulated miRNAs were measured by quantitative reverse transcription polymerase chain reaction (qRT-PCR). The regulations of signaling pathways by the combinatorial miRNAs were predicted by enrichment analysis tools.

resultsThirty-two differentially expressed (DE) miRNAs were identified to be AF-VHD-specific, some of which were new findings. These miRNAs interacted to form 5 combinations. qRT-PCR confirmed the different expression of several identified miRNAs, which illustrated the reliability and biomarker potentials of 32 dysregulation miRNAs. The biological characteristics of combinatorial miRNAs related to AF-VHD were highlighted. Twelve signaling pathways regulated by combinatorial miRNAs were predicted to be possibly associated with AF-VHD.

conclusionsThe AF-VHD-related signaling pathways regulated by combinatorial miRNAs may play an important role in the occurrence of AF-VHD. The work brings new insights into biomarkers and miRNA combination regulation mechanism in AF-VHD as well as further biological experiments.

Indexed as

AdultAgedAtrial FibrillationCase-Control StudiesFemaleHeart Valve DiseasesHumansMaleMicroRNAsMiddle AgedMitral ValveReverse Transcriptase Polymerase Chain ReactionSignal TransductionTranscriptomeMicroRNAs

Identifiers

PMID31479479
PMCPMC6719876
OpenAlexW2971894819

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.