Evidence map›Paper›PMID 23029284›Full record

ArticlePloS one2012

Comprehensive exploration of the effects of miRNA SNPs on monocyte gene expression.

Nicolas Greliche, Tanja Zeller, Philipp S Wild, Maxime Rotival, Arne Schillert, Andreas Ziegler, Cardiogenics Consortium, Panos Deloukas, Jeanette Erdmann, Christian Hengstenberg and 10 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 28% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 10 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. miR-23 regulate the pathogenesis of patients with coronary artery disease.International journal of clinical and experimental medicine · 2015
    Article
  6. Article
4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

20 authors at 12 institutions in 3 countries.

Nicolas GrelicheINSERM UMR_S 937, Pierre and Marie Curie University (UPMC, Paris 6), Paris, France.
Tanja Zeller
Philipp S Wild
Maxime Rotival
Arne Schillert
Andreas Ziegler
Cardiogenics Consortium
Panos Deloukas
Jeanette Erdmann
Christian Hengstenberg
Willem H Ouwehand
Nilesh J Samani
Heribert Schunkert
Thomas Munzel
Karl J Lackner
François Cambien
Alison H Goodall
Laurence Tiret
Stefan Blankenberg
David-Alexandre Trégouët
University of Lübeck · DESorbonne Université · FRUniversität Hamburg · DEUniversity Medical Center of the Johannes Gutenberg University Mainz · DEInserm · FRJohannes Gutenberg University Mainz · DENational Health Service · GBNational Institute for Health Research · GBUniversité Paris-Sud · FRUniversity of Leicester · GBUniversity of Regensburg · DEWellcome Sanger Institute · GB

Funding

British Heart Foundation RG/09/012/28096Wellcome Trust
6 · The paper itself

Abstract

We aimed to assess whether pri-miRNA SNPs (miSNPs) could influence monocyte gene expression, either through marginal association or by interacting with polymorphisms located in 3'UTR regions (3utrSNPs). We then conducted a genome-wide search for marginal miSNPs effects and pairwise miSNPs × 3utrSNPs interactions in a sample of 1,467 individuals for which genome-wide monocyte expression and genotype data were available. Statistical associations that survived multiple testing correction were tested for replication in an independent sample of 758 individuals with both monocyte gene expression and genotype data. In both studies, the hsa-mir-1279 rs1463335 was found to modulate in cis the expression of LYZ and in trans the expression of CNTN6, CTRC, COPZ2, KRT9, LRRFIP1, NOD1, PCDHA6, ST5 and TRAF3IP2 genes, supporting the role of hsa-mir-1279 as a regulator of several genes in monocytes. In addition, we identified two robust miSNPs × 3utrSNPs interactions, one involving HLA-DPB1 rs1042448 and hsa-mir-219-1 rs107822, the second the H1F0 rs1894644 and hsa-mir-659 rs5750504, modulating the expression of the associated genes.As some of the aforementioned genes have previously been reported to reside at disease-associated loci, our findings provide novel arguments supporting the hypothesis that the genetic variability of miRNAs could also contribute to the susceptibility to human diseases.

Indexed as

Polymorphism, Single NucleotideRNA InterferenceTranscriptome3' Untranslated RegionsAdultAgedCase-Control StudiesCoronary Artery DiseaseFemaleGene ExpressionGenome-Wide Association StudyHumansLeukocytes, MononuclearLinear ModelsLinkage DisequilibriumMale3' Untranslated RegionsMicroRNAs

Identifiers

PMID23029284
PMCPMC3448685
OpenAlexW2044423310

What OpenQuestion 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 OpenQuestion graph.