Evidence map›Paper›PMID 25583993›Full record

Trial reportCirculation. Cardiovascular genetics2015

DNA methylation of lipid-related genes affects blood lipid levels.

Liliane Pfeiffer, Simone Wahl, Luke C Pilling, Eva Reischl, Johanna K Sandling, Sonja Kunze, Lesca M Holdt, Anja Kretschmer, Katharina Schramm, Jerzy Adamski and 20 more

Open access · bronzeAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in Circulation. Cardiovascular genetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 123 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
123citing papers in PubMed, 6 pooled it
11.4field-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

123 citing papers in PubMed, 6 syntheses or guidelines pooled it, 200 citations in OpenAlex.

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63 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

30 authors at 5 institutions in 5 countries.

Liliane Pfeiffer
Simone Wahl
Luke C Pilling
Eva Reischl
Johanna K Sandling
Sonja Kunze
Lesca M Holdt
Anja Kretschmer
Katharina Schramm
Jerzy Adamski
Norman Klopp
Thomas Illig
Åsa K Hedman
Michael Roden
Dena G Hernandez
Andrew B Singleton
Wolfgang E Thasler
Harald Grallert
Christian Gieger
Christian Herder
Daniel Teupser
Christa Meisinger
Timothy D Spector
Florian Kronenberg
Holger Prokisch
David Melzer
Annette Peters
Panos Deloukas
Luigi Ferrucci
Melanie Waldenberger
Christ University · INDanieli (Italy) · ITPfeiffer University · USSingleton Hospital · GBUniversidad Dr. José Gregorio Hernández · VE

Funding

The Baltimore Longitudinal Study Of AgingZIAAG000015 · NIA · NATIONAL INSTITUTE ON AGING · PI SIMONSICK, ELEANOR MARIE · 2009 to 2025
$116.9M
THE BALTIMORE LONGITUDINAL STUDY OF HUMAN AGINGZ01AG000015 · NIA · NATIONAL INSTITUTE ON AGING · PI FERRUCCI, LUIGI · 1985 to 2008
$11.4M
British Heart Foundation RG/14/5/30893Intramural NIH HHS Z01 AG000015Wellcome TrustWellcome Trust 081917/Z/07/Z
6 · The paper itself

Abstract

backgroundEpigenetic mechanisms might be involved in the regulation of interindividual lipid level variability and thus may contribute to the cardiovascular risk profile. The aim of this study was to investigate the association between genome-wide DNA methylation and blood lipid levels high-density lipoprotein cholesterol, low-density lipoprotein cholesterol, triglycerides, and total cholesterol. Observed DNA methylation changes were also further analyzed to examine their relationship with previous hospitalized myocardial infarction. METHODS AND

resultsGenome-wide DNA methylation patterns were determined in whole blood samples of 1776 subjects of the Cooperative Health Research in the Region of Augsburg F4 cohort using the Infinium HumanMethylation450 BeadChip (Illumina). Ten novel lipid-related CpG sites annotated to various genes including ABCG1, MIR33B/SREBF1, and TNIP1 were identified. CpG cg06500161, located in ABCG1, was associated in opposite directions with both high-density lipoprotein cholesterol (β coefficient=-0.049; P=8.26E-17) and triglyceride levels (β=0.070; P=1.21E-27). Eight associations were confirmed by replication in the Cooperative Health Research in the Region of Augsburg F3 study (n=499) and in the Invecchiare in Chianti, Aging in the Chianti Area study (n=472). Associations between triglyceride levels and SREBF1 and ABCG1 were also found in adipose tissue of the Multiple Tissue Human Expression Resource cohort (n=634). Expression analysis revealed an association between ABCG1 methylation and lipid levels that might be partly mediated by ABCG1 expression. DNA methylation of ABCG1 might also play a role in previous hospitalized myocardial infarction (odds ratio, 1.15; 95% confidence interval=1.06-1.25).

conclusionsEpigenetic modifications of the newly identified loci might regulate disturbed blood lipid levels and thus contribute to the development of complex lipid-related diseases.

Indexed as

ATP-Binding Cassette TransportersEpigenesis, GeneticMyocardial InfarctionSterol Regulatory Element Binding Protein 1AdultAgedAged, 80 and overATP Binding Cassette Transporter, Subfamily G, Member 1Cohort StudiesDNA MethylationFemaleGenetic LociGermanyHumansLipidsMaleABCG1 protein, humanATP-Binding Cassette TransportersATP Binding Cassette Transporter, Subfamily G, Member 1LipidsSREBF1 protein, humanSterol Regulatory Element Binding Protein 1ABCG1DNA methylatioepidemiologygene expressionmyocardial infarction

Identifiers

PMID25583993
PMCPMC5012424
OpenAlexW2162198924

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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.