Evidence map›Paper›PMID 30507953›Full record

ArticlePloS one2018

RNA-sequencing analysis of umbilical cord plasma microRNAs from healthy newborns.

Gary P Brennan, Dimitrios M Vitsios, Sophie Casey, Ann-Marie Looney, Boubou Hallberg, David C Henshall, Geraldine B Boylan, Deirdre M Murray, Catherine Mooney

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-weighted citation impact, top 38% 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

4 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
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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

9 authors at 5 institutions in 3 countries.

Gary P BrennanDepartment of Physiology & Medical Physics, Royal College of Surgeons in Ireland, Dublin, Ireland.ORCID 0000-0002-4262-0481
Dimitrios M VitsiosEuropean Molecular Biology Laboratory-European Bioinformatics Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge CB10 1SD, United Kingdom.ORCID 0000-0002-8939-5445
Sophie CaseyINFANT Research Centre, University College Cork, Cork, Ireland.
Ann-Marie LooneyINFANT Research Centre, University College Cork, Cork, Ireland.
Boubou HallbergNeonatology, Karolinska University Hospital, Stockholm, Sweden.
David C HenshallDepartment of Physiology & Medical Physics, Royal College of Surgeons in Ireland, Dublin, Ireland.
Geraldine B BoylanINFANT Research Centre, University College Cork, Cork, Ireland.
Deirdre M MurrayINFANT Research Centre, University College Cork, Cork, Ireland.
Catherine MooneyFutureNeuro Research Centre, Royal College of Surgeons in Ireland, Dublin, Ireland.ORCID 0000-0002-7696-1364
University College Cork · IERoyal College of Surgeons in Ireland · IEEuropean Bioinformatics Institute · GBKarolinska University Hospital · SEUniversity College Dublin · IE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNAs are a class of small non-coding RNA that regulate gene expression at a post-transcriptional level. MicroRNAs have been identified in various body fluids under normal conditions and their stability as well as their dysregulation in disease has led to ongoing interest in their diagnostic and prognostic potential. Circulating microRNAs may be valuable predictors of early-life complications such as birth asphyxia or neonatal seizures but there are relatively few data on microRNA content in plasma from healthy babies. Here we performed small RNA-sequencing analysis of plasma processed from umbilical cord blood in a set of healthy newborns. MicroRNA levels in umbilical cord plasma of four male and four female healthy babies, from two different centres were profiled. A total of 1,004 individual microRNAs were identified, which ranged from 426 to 659 per sample, of which 269 microRNAs were common to all eight samples. Many of these microRNAs are highly expressed and consistent with previous studies using other high throughput platforms. While overall microRNA expression did not differ between male and female cord blood plasma, we did detect differentially edited microRNAs in female plasma compared to male. Of note, and consistent with other studies of this type, adenylation and uridylation were the two most prominent forms of editing. Six microRNAs, miR-128-3p, miR-29a-3p, miR-9-5p, miR-218-5p, 204-5p and miR-132-3p were consistently both uridylated and adenylated in female cord blood plasma. These results provide a benchmark for microRNA profiling and biomarker discovery using umbilical cord plasma and can be used as comparative data for future biomarker profiles from complicated births or those with early-life developmental disorders.

Indexed as

Adenosine MonophosphateBiomarkersCirculating MicroRNAFemaleFetal BloodGene Expression ProfilingGene Expression Regulation, DevelopmentalHumansInfant, NewbornMaleRNA EditingSex FactorsUridine MonophosphateAdenosine MonophosphateBiomarkersCirculating MicroRNAUridine Monophosphate

Identifiers

PMID30507953
PMCPMC6277075
OpenAlexW2903424668

What OpenQuestion holds

Textmetadata
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.