Evidence map›Paper›PMID 28871283›Full record

ArticleFrontiers in cardiovascular medicine2017

GPla Polymorphisms Are Associated with Outcomes in Patients at High Cardiovascular Risk.

Dominik Rath, Elke Schaeffeler, Stefan Winter, Semjon Levertov, Karin Müller, Michal Droppa, Fabian Stimpfle, Harald F Langer, Meinrad Gawaz, Matthias Schwab and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cardiovascular medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.2field-weighted citation impact, top 42% 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

5 citing papers in PubMed, 13 citations in OpenAlex.

  1. Platelet versus plasma CXCL14, coronary artery disease, and clinical outcomes.Research and practice in thrombosis and haemostasis · 2023
    Article
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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

11 authors at 2 institutions in 1 country.

Dominik RathDepartment of Cardiology, University Hospital Tuebingen, Tuebingen, Germany.
Elke SchaeffelerDr. Margarete-Fischer-Bosch Institute of Clinical Pharmacology, Stuttgart, Germany.
Stefan WinterDr. Margarete-Fischer-Bosch Institute of Clinical Pharmacology, Stuttgart, Germany.
Semjon LevertovDepartment of Cardiology, University Hospital Tuebingen, Tuebingen, Germany.
Karin MüllerDepartment of Cardiology, University Hospital Tuebingen, Tuebingen, Germany.
Michal DroppaDepartment of Cardiology, University Hospital Tuebingen, Tuebingen, Germany.
Fabian StimpfleDepartment of Cardiology, University Hospital Tuebingen, Tuebingen, Germany.
Harald F LangerDepartment of Cardiology, University Hospital Tuebingen, Tuebingen, Germany.
Meinrad GawazDepartment of Cardiology, University Hospital Tuebingen, Tuebingen, Germany.
Matthias SchwabDr. Margarete-Fischer-Bosch Institute of Clinical Pharmacology, Stuttgart, Germany.
Tobias GeislerDepartment of Cardiology, University Hospital Tuebingen, Tuebingen, Germany.
University of Tübingen · DEDr. Margarete Fischer-Bosch-Institute of Clinical Pharmacology · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPlatelet membrane glycoprotein receptors mediate thrombus formation. GP Ia/IIa is an essential platelet integrin receptor. Single-nucleotide polymorphisms (SNPs) of the GP Ia/IIa gene alter GP Ia/IIa expression; however, their influence on cardiovascular disease remains unclear. This study aimed to investigate the effect of the GP Ia/IIa SNPs rs1126643 and rs1062535 on clinical outcomes in a large collective including high-risk patients with cardiovascular disease. METHODS AND

resultsGP Ia SNP analysis was performed in 943 patients with symptomatic coronary artery disease. All patients were tracked for all-cause death, myocardial infarction, and ischemic stroke for 360 days. Homozygous carriers of the minor allele showed significantly worse event-free survival when compared with major allele carriers in the complete collective as well as in the subset of high-risk patients (carrying all of the following three risk factors: diabetes type II, hypertension, and hyperlipidemia). There was no significant difference in the subset of low-risk patients (carrying none of the three risk factors).

conclusionsGPla SNPs are associated with cardiovascular prognosis especially in high-risk patients. Identification of GPIa SNPs is of importance to tailor therapies in patients at already high cardiovascular risk.

Indexed as

clinical studycoronary artery diseaseintegrin alpha2polymorphismsingle nucleotidethromboembolism

Identifiers

PMID28871283
PMCPMC5566565
OpenAlexW2746176447

What OpenQuestion holds

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LicenceCC BY
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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.