Evidence map›Paper›PMID 25656948›Full record

ArticleExperimental & molecular medicine2015

MiR-34a, miR-21 and miR-23a as potential biomarkers for coronary artery disease: a pilot microarray study and confirmation in a 32 patient cohort.

Hui Han, Guangjin Qu, Chenghua Han, Yuhong Wang, Tingting Sun, Fengqing Li, Junxiao Wang, Shanshun Luo

Open access · goldAbstract read
In one paragraph

Article in Experimental & molecular medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 11% 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

58 citing papers in PubMed, 1 synthesis or guideline pooled it, 94 citations in OpenAlex.

  1. Pooled it
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  7. Observational
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  19. Genomic Variants and Multilevel Regulation ofJournal of cardiovascular development and disease · 2021
    Review
  20. MicroRNA-34a: the bad guy in age-related vascular diseases.Cellular and molecular life sciences : CMLS · 2021
    Review
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 2 institutions in 1 country.

Hui HanDepartment of Gerontology, the First Hospital of Harbin Medical University, Harbin, China.
Guangjin QuDepartment of Gerontology, the First Hospital of Harbin Medical University, Harbin, China.
Chenghua HanDepartment of Natural Product Chemistry, the Daqing Campus of Harbin Medical University, Daqing, China.
Yuhong WangDepartment of Gerontology, the First Hospital of Harbin Medical University, Harbin, China.
Tingting SunDepartment of Gerontology, the First Hospital of Harbin Medical University, Harbin, China.
Fengqing LiDepartment of Gerontology, the First Hospital of Harbin Medical University, Harbin, China.
Junxiao WangDepartment of Gerontology, the First Hospital of Harbin Medical University, Harbin, China.
Shanshun LuoDepartment of Gerontology, the First Hospital of Harbin Medical University, Harbin, China.
First Affiliated Hospital of Harbin Medical University · CNHarbin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this study was to investigate the expression of circulating microRNAs (miRNAs) in apolipoprotein E (apoE) knockout mice (apoE(-/-)) and to validate the role of these miRNAs in human coronary artery disease (CAD). Pooled plasma from 10 apoE(-/-) mice and 10 healthy C57BL/6 (B6) mice was used to perform the microarray analysis. The results showed that miR-34a, miR-21, miR-23a, miR-30a and miR-106b were differentially expressed in apoE(-/-) mice, and these expression changes were confirmed by real-time quantitative reverse-transcription PCR. Then, miR-34a, miR-21, miR-23a, miR-30a and miR-106b were detected in the plasma of 32 patients with CAD and of 20 healthy controls. Only miR-34a, miR-21 and miR-23a were significantly differentially expressed in the plasma of CAD patients (all P<0.01). In conclusion, miR-34a, miR-21 and miR-23a were elevated in CAD patients, which means that these miRNAs might serve as biomarkers of CAD development and progression.

Indexed as

AgedAnimalsApolipoproteins EBiomarkersCase-Control StudiesCoronary Artery DiseaseDisease Models, AnimalGene Expression ProfilingGene Expression RegulationHumansMaleMiceMice, KnockoutMicroRNAsMiddle AgedPilot ProjectsApolipoproteins EBiomarkersMicroRNAsMIRN21 microRNA, humanMIRN23a microRNA, humanMIRN34 microRNA, human

Identifiers

PMID25656948
PMCPMC4346489
OpenAlexW2073175477

What OpenQuestion holds

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LicenceCC BY-NC-SA
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 OpenQuestion graph.