Evidence map›Paper›PMID 28685248›Full record

ArticleMolecular biology reports2017

Genetic risk factors for myocardial infarction more clearly manifest for early age of first onset.

Boris V Titov, German J Osmak, Natalia A Matveeva, Nino G Kukava, Roman M Shakhnovich, Alexander V Favorov, Mikhail Ya Ruda, Olga O Favorova

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular biology reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 26% 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

3 citing papers in PubMed, 14 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
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 3 institutions in 2 countries.

Boris V TitovInstitute of Experimental Cardiology, Russian Cardiology Scientific and Production Center, Moscow, Russia. titovborisvas@gmail.com.
German J OsmakInstitute of Experimental Cardiology, Russian Cardiology Scientific and Production Center, Moscow, Russia.
Natalia A MatveevaInstitute of Experimental Cardiology, Russian Cardiology Scientific and Production Center, Moscow, Russia.
Nino G KukavaInstitute of Experimental Cardiology, Russian Cardiology Scientific and Production Center, Moscow, Russia.
Roman M ShakhnovichDepartment of Emergency Cardiology, Russian Cardiology Scientific and Production Center, Moscow, Russia.
Alexander V FavorovDepartment of Computational Biology, Vavilov Institute of General Genetics, Russian Academy of Sciences, Moscow, Russia.
Mikhail Ya RudaDepartment of Emergency Cardiology, Russian Cardiology Scientific and Production Center, Moscow, Russia.
Olga O FavorovaInstitute of Experimental Cardiology, Russian Cardiology Scientific and Production Center, Moscow, Russia.
Institute of Experimental Cardiology · RUPirogov Russian National Research Medical University · RUJohns Hopkins Medicine · US

Funding

Russian Science Foundation 16-14-10251
6 · The paper itself

Abstract

Epidemiological genetics established that heritability in determining the risk of myocardial infarction (MI) is substantially greater when MI occurs early in life. However, the genetic architecture of early-onset and late-onset MI was not compared. We analyzed genotype frequencies of SNPs in/near 20 genes whose protein products are involved in the pathogenesis of atherosclerosis in two groups of Russian patients with MI: the first group included patients with age of first MI onset <60 years (N = 230) and the second group with onset ≥60 years (N = 174). The control group of corresponding ethnicity consisted of 193 unrelated volunteers without cardiovascular diseases (93 individuals were over 60 years). We found that in the group of patients with age of onset <60 years, SNPs FGB rs1800788*T, TGFB1 rs1982073*T/T, ENOS rs2070744*C and CRP rs1130864*T/T were associated with risk of MI, whereas in patients with age of onset ≥60 years, only TGFB1 rs1982073*T/T was associated with risk of MI. Using APSampler software, we found composite markers associated with MI only in patients with early onset: FGB rs1800788*T + TGFB1 rs1982073*T; FGB rs1800788*T + LPL rs328*C + IL4 rs2243250*C; FGB rs1800788*T + ENOS rs2070744*C (Fisher p values of 1.4 × 10

Indexed as

AdultAgedAged, 80 and overAge FactorsAllelesAtherosclerosisBiomarkersFemaleGene FrequencyGenetic Association StudiesGenetic Predisposition to DiseaseHumansMaleMiddle AgedMyocardial InfarctionPolymorphism, Single NucleotideBiomarkersAge of first onsetGenetic markersMyocardial infarctionRisk prediction

Identifiers

PMID28685248
OpenAlexW2730529023

What OpenQuestion holds

Textmetadata
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.