Evidence map›Paper›PMID 29927903›Full record

ArticleMedical science monitor : international medical journal of experimental and clinical research2018

Expression of the Marburg I Single Nucleotide Polymorphism (MI-SNP) and the Marburg II Single Nucleotide Polymorphism (MII-SNP) of the Factor VII-Activating Protease (FSAP) Gene and Risk of Coronary Artery Disease (CAD): A Pilot Study in a Single Population.

Mariana S Parahuleva, Bernhard Schieffer, Michael Klassen, Michael Worsch, Behnoush Parviz, Hans Hölschermann

Open access · hybridAbstract read
In one paragraph

Article in Medical science monitor : international medical journal of experimental and clinical research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.5field-weighted citation impact, top 33% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. 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

6 authors at 2 institutions in 1 country.

Mariana S ParahulevaDepartment of Internal Medicine/Cardiology and Angiology, University Hospital of Giessen and Marburg, Marburg, Germany.
Bernhard SchiefferDepartment of Internal Medicine/Cardiology and Angiology, University Hospital of Giessen and Marburg, Marburg, Germany.
Michael KlassenDepartment of Internal Medicine I, Cardiology and Angiology, University Hospital of Giessen and Marburg, Giessen, Germany.
Michael WorschDepartment of Internal Medicine I, Cardiology and Angiology, University Hospital of Giessen and Marburg, Giessen, Germany.
Behnoush ParvizDepartment of Internal Medicine I, Cardiology and Angiology, University Hospital of Giessen and Marburg, Giessen, Germany.
Hans HölschermannDepartment of Cardiology, Hospital Bad Homburg Internal Medicine I, Bad Homburg, Germany.
Universitätsklinikum Gießen und Marburg · DEAccadis Hochschule Bad Homburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND Factor VII-activating protease (FSAP) has a role in vascular inflammation and may have a role coronary artery disease (CAD). The aim of this study was to investigate the association between two naturally occurring single nucleotide polymorphisms (SNPs) in the FSAP gene and the risk of coronary artery disease (CAD). MATERIAL AND METHODS Of 733 patients, 173 patients had symptoms of angina, and 560 patients had CAD confirmed by coronary angiography. All patients were genotyped for SNPs of the FSAP gene, Marburg I (MI-SNP) and Marburg II (MII-SNP), using 5' exonuclease TaqMan assays. Logistic regression analysis was used to evaluate the association between two gene polymorphisms, metabolic and other cardiovascular risk factors in patients with CAD. RESULTS The presence of MI-SNP and MII-SNP FSAP gene polymorphisms were not associated with the presence of CAD. However, the MII-SNP polymorphism was significantly associated with a reduced risk of developing CAD (OR=0.422; 95% CI, 0.194-0.920; P=0.035); the MI-SNP polymorphism was associated with absence of hyperlipoproteinemia (OR=0.601; 95% CI, 0.344-1.051; P=0.074). There was no significant association between expression of the MI-SNP and MII-SNP FSAP gene polymorphisms and the incidence of myocardial infarction, or of a history of diabetes mellitus, arterial hypertension, obesity, or smoking. CONCLUSIONS The MI-SNP and MII-SNP FSAP gene polymorphisms were not predictive or prognostic biomarkers for CAD or its main risk factors. However, the presence of the MII-SNP polymorphism was associated with a reduced risk of developing CAD.

Indexed as

Genetic Predisposition to DiseaseCoronary Artery DiseaseGenetic Association StudiesHumansPilot ProjectsPolymorphism, Single NucleotideRisk FactorsSerine EndopeptidasesHABP2 protein, humanSerine Endopeptidases

Identifiers

PMID29927903
PMCPMC6044212
OpenAlexW2809124561

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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.