Evidence map›Paper›PMID 28515798›Full record

Trial reportClinical epigenetics2017

Epigenome-wide association of myocardial infarction with DNA methylation sites at loci related to cardiovascular disease.

Masahiro Nakatochi, Sahoko Ichihara, Ken Yamamoto, Keiko Naruse, Shigeki Yokota, Hiroyuki Asano, Tatsuaki Matsubara, Mitsuhiro Yokota

Open access · goldAbstract readClinical Trial
In one paragraph

Trial report in Clinical epigenetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed, 2 pooled it
4.9field-weighted citation impact, top 4% 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

55 citing papers in PubMed, 2 syntheses or guidelines pooled it, 126 citations in OpenAlex.

  1. Pooled it
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  15. Epigenetics in Precision Nutrition.Journal of personalized medicine · 2022
    Review
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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

8 authors at 5 institutions in 1 country.

Masahiro Nakatochi *Statistical Analysis Section, Center for Advanced Medicine and Clinical Research, Nagoya University Hospital, Nagoya, 466-8550 Japan.
Sahoko Ichihara *Department of Environmental and Preventive Medicine, Jichi Medical University School of Medicine, 3311-1 Yakushiji, Shimotsuke, 329-0498 Japan.
Ken YamamotoDepartment of Medical Biochemistry, Kurume University School of Medicine, Kurume, 830-0011 Japan.
Keiko NaruseDepartment of Internal Medicine, School of Dentistry, Aichi Gakuin University, 2-11 Suemori-dori, Chikusa-ku, Nagoya, 464-8651 Japan.
Shigeki YokotaDepartment of Internal Medicine, Iwakura Hospital, Iwakura, 482-0015 Japan.
Hiroyuki AsanoDepartment of Internal Medicine, Iwakura Hospital, Iwakura, 482-0015 Japan.
Tatsuaki MatsubaraDepartment of Internal Medicine, School of Dentistry, Aichi Gakuin University, 2-11 Suemori-dori, Chikusa-ku, Nagoya, 464-8651 Japan.
Mitsuhiro YokotaDepartment of Genome Science, School of Dentistry, Aichi Gakuin University, 2-11 Suemori-dori, Chikusa-ku, Nagoya, 464-8651 Japan.
Aichi Gakuin University · JPShinKokura Hospital · JPJichi Medical University · JPKurume University Medical Center · JPNagoya University Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDevelopment of cardiovascular disease (CVD), including coronary artery disease, arrhythmia, and ischemic stroke, depends on environmental and genetic factors. To investigate the epigenetic basis of myocardial infarction (MI), we performed an epigenome-wide association study for this condition in elderly Japanese subjects. A total of 192 case subjects with MI and 192 control subjects were recruited from hospital attendees and the general population, respectively. Genome-wide DNA methylation (DNAm) profiles for DNA isolated from whole blood were obtained by analysis with an Infinium HumanMethylation450 BeadChip. The relation of DNAm sites found to be significantly associated with MI to nearby single nucleotide polymorphisms (SNPs) previously shown to be associated with CVD was assessed in the control group.

findingsThree DNAm sites (cg06642177, cg07786668, cg17218495) showed genome-wide significant associations with MI (

conclusionsWe identified two DNAm sites-cg07786668 in

Indexed as

DNA MethylationAgedAsian PeopleCross-Sectional StudiesDNA HelicasesEpigenesis, GeneticEpigenomicsGenetic Predisposition to DiseaseGenome-Wide Association StudyHomeodomain ProteinsHumansJapanMaleMiddle AgedMyocardial InfarctionNuclear ProteinsDNA HelicasesHomeodomain ProteinsNuclear ProteinsSMARCA4 protein, humanTranscription FactorsZFHX3 protein, humanCardiovascular diseaseDNA methylationEpigenome-wide association studyMyocardial infarctionSingle nucleotide polymorphism

Identifiers

PMID28515798
PMCPMC5432989
OpenAlexW2613708736

What OpenQuestion holds

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LicenceCC BY
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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.