Evidence map›Paper›PMID 36683124›Full record

Observational studyJournal of applied genetics2023

Total impact of oxidative stress genes on cardiovascular events-a 7-year follow-up study.

Milena Racis, Anna Stanisławska-Sachadyn, Wojciech Sobiczewski, Marcin Wirtwein, Michał Krzemiński, Andrzej Rynkiewicz, Bartosz Wasąg, Miłosz Jaguszewski, Marcin Gruchała

Open access · hybridAbstract readObservational Study
In one paragraph

Observational study in Journal of applied genetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.4field-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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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

9 authors at 3 institutions in 1 country.

Milena RacisFirst Department of Cardiology, Medical University of Gdansk, Ul. Smoluchowskiego 17, 80-214, Gdańsk, Poland. milmil@gumed.edu.pl.ORCID http://orcid.org/0000-0003-0075-8666
Anna Stanisławska-SachadynDepartment of Molecular Biotechnology and Microbiology, Gdansk University of Technology, Ul. Narutowicza 11/12, 80-233, Gdańsk, Poland.
Wojciech SobiczewskiFirst Department of Cardiology, Medical University of Gdansk, Ul. Smoluchowskiego 17, 80-214, Gdańsk, Poland.
Marcin WirtweinDepartment of Pharmacology, Medical University of Gdansk, Ul. Dębowa 23, 80-204, Gdańsk, Poland.
Michał KrzemińskiInstitute of Applied Mathematics, Faculty of Applied Physics and Mathematics, Gdansk University of Technology, 80-233, Gdańsk, Poland.
Andrzej RynkiewiczDepartment of Cardiology and Cardiosurgery, University of Warmia and Mazury in Olsztyn, Al. Warszawska 30, 10-082, Olsztyn, Poland.
Bartosz WasągDepartment of Biology and Genetics, Medical University of Gdansk, Ul. Dębinki 1, 80-211, Gdańsk, Poland.
Miłosz JaguszewskiFirst Department of Cardiology, Medical University of Gdansk, Ul. Smoluchowskiego 17, 80-214, Gdańsk, Poland.
Marcin GruchałaFirst Department of Cardiology, Medical University of Gdansk, Ul. Smoluchowskiego 17, 80-214, Gdańsk, Poland.
Gdańsk Medical University · PLGdańsk University of Technology · PLUniversity of Warmia and Mazury in Olsztyn · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cardiovascular (CV) events are the number one cause of lifetime disability and deaths worldwide. It is well known that traditional risk factors do not fully correlate with clinical outcomes; therefore, searching for other markers that would explain CV events' occurrence seems essential. Of importance, one of the main factors at the origin of CV events is oxidative stress, causing inflammation and atherosclerotic plaque instability. Therefore, the present study was conducted to evaluate eight carefully selected genetic polymorphisms related to oxidative stress as risk modifiers for CV events. A cohort of 1020 patients with coronary atherosclerosis was analysed in a 7-year follow-up observational study. The following end points were assessed: CV death, myocardial infarction (MI) and a combined end point of CV death/MI/stroke. Our results show that single polymorphisms are not significant cardiovascular disease risk factors, but genetic risk score (GRS), defined as the accumulation of our eight studied polymorphisms, was significantly associated with the three. Specifically, low GRS was associated with a higher risk of CV death, MI and CV death/MI/stroke. In conclusion, when regarding CV events, GRS investigated here can become clinically meaningful and undoubtedly adds to the knowledge in stratifying the risk of CV events.

Indexed as

Myocardial InfarctionStrokeFollow-Up StudiesHumansPolymorphism, GeneticRisk FactorsCardiovascular diseaseCV eventsGene polymorphismGRSOxidative stressSNP

Identifiers

PMID36683124
PMCPMC10076362
OpenAlexW4317716383

What OpenQuestion holds

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LicenceCC BY
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.