Evidence map›Paper›PMID 31607954›Full record

ArticleFrontiers in physiology2019

Integrative Analysis of miRNA and mRNA Expression Profiles Associated With Human Atrial Aging.

Yan Yao, Chenxi Jiang, Fan Wang, Han Yan, Deyong Long, Jinghua Zhao, Jiangang Wang, Chunxiao Zhang, Yang Li, Xiaoli Tian and 3 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in physiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.8field-weighted citation impact, top 32% 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

10 citing papers in PubMed, 13 citations in OpenAlex.

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  7. Evaluating the Effect of 3'-UTR Variants inCurrent issues in molecular biology · 2021
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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

13 authors at 6 institutions in 2 countries.

Yan YaoDepartment of Cardiology, Beijing Anzhen Hospital, Capital Medical University, Beijing, China.
Chenxi JiangDepartment of Cardiology, Beijing Anzhen Hospital, Capital Medical University, Beijing, China.
Fan WangCenter for Cardiovascular Genetics, Department of Molecular Cardiology, Lerner Research Institute, Cleveland Clinic, Case Western Reserve University, Cleveland, OH, United States.
Han YanDepartment of Human Population Genetics and Beijing Key Laboratory of Cardiometabolic Molecular Medicine, Institute of Molecular Medicine, Peking University, Beijing, China.
Deyong LongDepartment of Cardiology, Beijing Anzhen Hospital, Capital Medical University, Beijing, China.
Jinghua ZhaoDepartment of Cardiology, Beijing Anzhen Hospital, Capital Medical University, Beijing, China.
Jiangang WangDepartment of Cardiac Surgery, Beijing Anzhen Hospital, Capital Medical University, Beijing, China.
Chunxiao ZhangDepartment of Cardiac Surgery, Beijing Anzhen Hospital, Capital Medical University, Beijing, China.
Yang LiDepartment of Human Population Genetics and Beijing Key Laboratory of Cardiometabolic Molecular Medicine, Institute of Molecular Medicine, Peking University, Beijing, China.
Xiaoli TianDepartment of Human Population Genetics and Beijing Key Laboratory of Cardiometabolic Molecular Medicine, Institute of Molecular Medicine, Peking University, Beijing, China.
Qing K WangCenter for Cardiovascular Genetics, Department of Molecular Cardiology, Lerner Research Institute, Cleveland Clinic, Case Western Reserve University, Cleveland, OH, United States.
Gang WuDepartment of Cardiology, Renmin Hospital of Wuhan University, Wuhan, China.
Zhihui ZhangDepartment of Cardiology, The Third Xiangya Hospital of Central South University, Changsha, China.
Beijing Anzhen Hospital · CNCapital Medical University · CNPeking University · CNCase Western Reserve University · USCentral South University · CNWuhan University · CN

Funding

GENES FOR VASCULAR MORPHOGENESIS: A GENETIC APPROACHR01HL065630 · NHLBI · CLEVELAND CLINIC FOUNDATION · PI WANG, QING KENNETH · 2000 to 2003
$1.4M
NHLBI NIH HHS R01 HL065630
6 · The paper itself

Abstract

backgroundLimited findings have been reported to systematically study miRNA and mRNA expression profiles in aged human atria. In this study, we aimed to identify miRNAs, genes, and miRNA-mRNA interaction networks for human atrial aging (AA).

methodsRight atrial appendages from twelve patients who received aortic valve replacement were subjected to miRNA-seq and RNA-seq. All the patients were in sinus rhythm (SR) and stratified by age into four groups. Differential expression analysis was carried out to identify miRNAs and genes for human AA. The miRNA-mRNA interactions for human AA were identified by Pearson correlation analysis and miRNA target prediction programs.

resultsSeven miRNAs (4 upregulation and 3 downregulation) and 42 genes (23 upregulation and 19 downregulation) were differentially expressed in human right atrial tissues between older samples and younger samples. Bioinformatic analysis identified 114 pairs of putative miRNA-mRNA interactions on AA and four types of correlation. Pathway enrichment analysis identified over 40 significant pathways and the top three pathways included rhythmic process (

conclusionOur study revealed novel miRNA-mRNA interaction networks and signaling pathways for AA, providing novel insights into the development of human AA. Future studies are needed to investigate the potential significance of these miRNA-mRNA interactions in human AA or AA-related cardiovascular diseases.

Indexed as

atrial aginginteractionmiRNAmRNAsignaling pathway

Identifiers

PMID31607954
PMCPMC6761282
OpenAlexW2974708160

What OpenQuestion holds

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LicenceCC BY
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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.