Evidence map›Paper›PMID 20502693›Full record

ArticlePloS one2010

Genetics and beyond--the transcriptome of human monocytes and disease susceptibility.

Tanja Zeller, Philipp Wild, Silke Szymczak, Maxime Rotival, Arne Schillert, Raphaele Castagne, Seraya Maouche, Marine Germain, Karl Lackner, Heidi Rossmann and 17 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 400 papers, 19 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
400citing papers in PubMed, 19 pooled it
22.2field-weighted citation impact, top 1% 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

400 citing papers in PubMed, 19 syntheses or guidelines pooled it, 599 citations in OpenAlex.

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  14. Interaction between variants in CLU and MS4A4E modulates Alzheimer's disease risk.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2016
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  20. Genetic Variants inDiabetes · 2018
    Trial

340 more citing papers are in PubMed but not listed here.

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

27 authors at 11 institutions in 3 countries.

Tanja ZellerMedizinische Klinik und Poliklinik, Johannes-Gutenberg Universität Mainz, Mainz, Germany.
Philipp Wild
Silke Szymczak
Maxime Rotival
Arne Schillert
Raphaele Castagne
Seraya Maouche
Marine Germain
Karl Lackner
Heidi Rossmann
Medea Eleftheriadis
Christoph R Sinning
Renate B Schnabel
Edith Lubos
Detlev Mennerich
Werner Rust
Claire Perret
Carole Proust
Viviane Nicaud
Joseph Loscalzo
Norbert Hübner
David Tregouet
Thomas Münzel
Andreas Ziegler
Laurence Tiret
Stefan Blankenberg
François Cambien
Inserm · FRJohannes Gutenberg University Mainz · DEKlinik und Poliklinik für Psychosomatische Medizin und Psychotherapie · DESorbonne Université · FRBoehringer Ingelheim (Germany) · DEUniversity Medical Center of the Johannes Gutenberg University Mainz · DEBrigham and Women's Hospital · USInstitut für Medizinische Informatik, Biometrie und Epidemiologie · DEMax Delbrück Center · DEUniversity Hospital Schleswig-Holstein · DEUniversity of Lübeck · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundVariability of gene expression in human may link gene sequence variability and phenotypes; however, non-genetic variations, alone or in combination with genetics, may also influence expression traits and have a critical role in physiological and disease processes. METHODOLOGY/PRINCIPAL

findingsTo get better insight into the overall variability of gene expression, we assessed the transcriptome of circulating monocytes, a key cell involved in immunity-related diseases and atherosclerosis, in 1,490 unrelated individuals and investigated its association with >675,000 SNPs and 10 common cardiovascular risk factors. Out of 12,808 expressed genes, 2,745 expression quantitative trait loci were detected (P<5.78x10(-12)), most of them (90%) being cis-modulated. Extensive analyses showed that associations identified by genome-wide association studies of lipids, body mass index or blood pressure were rarely compatible with a mediation by monocyte expression level at the locus. At a study-wide level (P<3.9x10(-7)), 1,662 expression traits (13.0%) were significantly associated with at least one risk factor. Genome-wide interaction analyses suggested that genetic variability and risk factors mostly acted additively on gene expression. Because of the structure of correlation among expression traits, the variability of risk factors could be characterized by a limited set of independent gene expressions which may have biological and clinical relevance. For example expression traits associated with cigarette smoking were more strongly associated with carotid atherosclerosis than smoking itself. CONCLUSIONS/SIGNIFICANCE: This study demonstrates that the monocyte transcriptome is a potent integrator of genetic and non-genetic influences of relevance for disease pathophysiology and risk assessment.

Indexed as

Gene Expression ProfilingGenetic Predisposition to DiseaseAdultAgedAtherosclerosisBase SequenceCell MovementChromosomes, Human, Pair 21DNA ProbesFemaleGene Expression RegulationGenetic VariationGenome, HumanGenome-Wide Association StudyHumansImmunityDNA Probes

Identifiers

PMID20502693
PMCPMC2872668
OpenAlexW1984939442

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.