Evidence map›Paper›PMID 34668383›Full record

ArticleJournal of the American Heart Association2021

Genetic Profile of Endotoxemia Reveals an Association With Thromboembolism and Stroke.

Jaakko Leskelä, Iiro Toppila, Mari-Anne Härma, Teemu Palviainen, Aino Salminen, Niina Sandholm, Milla Pietiäinen, Elisa Kopra, Jean-Paul Pais de Barros, FinnGen and 14 more

Open access · goldAbstract read
In one paragraph

Article in Journal of the American Heart Association, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

14 citing papers in PubMed, 24 citations in OpenAlex.

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  9. Human serum proteomics reveals a molecular signature after one night of sleep deprivation.Sleep advances : a journal of the Sleep Research Society · 2024
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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

24 authors at 4 institutions in 3 countries.

Jaakko LeskeläOral and Maxillofacial Diseases University of Helsinki and Helsinki University Hospital Helsinki Finland.ORCID 0000-0001-9670-339X
Iiro ToppilaFolkhälsan Institute of GeneticsFolkhälsan Research Center Helsinki Finland.
Mari-Anne HärmaFolkhälsan Institute of GeneticsFolkhälsan Research Center Helsinki Finland.
Teemu PalviainenInstitute for Molecular Medicine Finland University of Helsinki Finland.ORCID 0000-0002-7847-8384
Aino SalminenOral and Maxillofacial Diseases University of Helsinki and Helsinki University Hospital Helsinki Finland.
Niina SandholmFolkhälsan Institute of GeneticsFolkhälsan Research Center Helsinki Finland.ORCID 0000-0003-4322-6942
Milla PietiäinenOral and Maxillofacial Diseases University of Helsinki and Helsinki University Hospital Helsinki Finland.ORCID 0000-0002-4875-0682
Elisa KopraOral and Maxillofacial Diseases University of Helsinki and Helsinki University Hospital Helsinki Finland.
Jean-Paul Pais de BarrosINSERM UMR1231 Dijon France.
FinnGen
Mariann I LasseniusFolkhälsan Institute of GeneticsFolkhälsan Research Center Helsinki Finland.
Anmol KumarFolkhälsan Institute of GeneticsFolkhälsan Research Center Helsinki Finland.ORCID 0000-0002-5626-4190
Valma HarjutsaloFolkhälsan Institute of GeneticsFolkhälsan Research Center Helsinki Finland.ORCID 0000-0003-3568-9779
Kajsa RoslundFolkhälsan Institute of GeneticsFolkhälsan Research Center Helsinki Finland.ORCID 0000-0002-2271-611X
Carol ForsblomFolkhälsan Institute of GeneticsFolkhälsan Research Center Helsinki Finland.ORCID 0000-0002-3354-7454
Anu LoukolaInstitute for Molecular Medicine Finland University of Helsinki Finland.
Aki S HavulinnaInstitute for Molecular Medicine Finland University of Helsinki Finland.ORCID 0000-0002-4787-8959
Laurent LagrostINSERM UMR1231 Dijon France.
Veikko SalomaaDepartment of Public Health Solutions Finnish Institute for Health and Welfare Helsinki Finland.ORCID 0000-0001-7563-5324
Per-Henrik GroopFolkhälsan Institute of GeneticsFolkhälsan Research Center Helsinki Finland.
Markus PerolaGenomics and Biomarkers Unit Department of Health Finnish Institute for Health and Welfare Helsinki Finland.ORCID 0000-0003-4842-1667
Jaakko KaprioInstitute for Molecular Medicine Finland University of Helsinki Finland.ORCID 0000-0002-3716-2455
Markku LehtoFolkhälsan Institute of GeneticsFolkhälsan Research Center Helsinki Finland.
Pirkko J PussinenOral and Maxillofacial Diseases University of Helsinki and Helsinki University Hospital Helsinki Finland.ORCID 0000-0003-3563-1876
University of Helsinki · FIInserm · FRFinnish Institute for Health and Welfare · FIFinnish Institute of Occupational Health · FI

Funding

The development of alcohol misuse and related problems from adolescence to early midlifeR01AA015416 · NIAAA · WASHINGTON UNIVERSITY · PI DICK, DANIELLE M, SALVATORE, JESSICA E · 2005 to 2024
$7.6M
A GENOME-WIDE METHYLATION STUDY ON ESSENTIAL HYPERTENSIONR01HL104125 · NHLBI · AUGUSTA UNIVERSITY · PI WANG, XIAOLING · 2011 to 2015
$2.9M
Twin, molecular, and developmental approaches to understanding alcohol misuseK02AA018755 · NIAAA · VIRGINIA COMMONWEALTH UNIVERSITY · PI DICK, DANIELLE M · 2010 to 2019
$1.3M
NHLBI NIH HHS R01 HL104125NIAAA NIH HHS K02 AA018755NIAAA NIH HHS R01 AA015416Wellcome Trust
6 · The paper itself

Abstract

Background Translocation of lipopolysaccharide from gram-negative bacteria into the systemic circulation results in endotoxemia. In addition to acute infections, endotoxemia is detected in cardiometabolic disorders, such as cardiovascular diseases and obesity. Methods and Results We performed a genome-wide association study of serum lipopolysaccharide activity in 11 296 individuals from 6 different Finnish study cohorts. Endotoxemia was measured by limulus amebocyte lysate assay in the whole population and by 2 other techniques (Endolisa and high-performance liquid chromatography/tandem mass spectrometry) in subpopulations. The associations of the composed genetic risk score of endotoxemia and thrombosis-related clinical end points for 195 170 participants were analyzed in FinnGen. Lipopolysaccharide activity had a genome-wide significant association with 741 single-nucleotide polymorphisms in 5 independent loci, which were mainly located at genes affecting the contact activation of the coagulation cascade and lipoprotein metabolism and explained 1.5% to 9.2% of the variability in lipopolysaccharide activity levels. The closest genes included

Indexed as

EndotoxemiaStrokeVenous ThromboembolismGenetic ProfileGenome-Wide Association StudyHumansLipopolysaccharidesLipoproteinsThrombosisLipopolysaccharidesLipoproteinscoagulationcontact activationendotoxingenegenome‐wide association studylipopolysaccharide

Identifiers

PMID34668383
PMCPMC8751832
OpenAlexW3193484779

What OpenQuestion holds

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LicenceCC BY-NC
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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.