Evidence map›Paper›PMID 29915175›Full record

ArticleScientific reports2018

Value of multilocus genetic risk score for atrial fibrillation in end-stage kidney disease patients in a Polish population.

Marek Saracyn, Bartłomiej Kisiel, Artur Bachta, Maria Franaszczyk, Dorota Brodowska-Kania, Wawrzyniec Żmudzki, Konrad Szymański, Antoni Sokalski, Wiesław Klatko, Marek Stopiński and 10 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.7field-weighted citation impact, top 27% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Review
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

20 authors at 6 institutions in 2 countries.

Marek SaracynDepartment of Internal Diseases, Nephrology and Dialysis; Military Institute of Medicine, Szaserów 128, 04-141, Warsaw, Poland. msaracyn@interia.pl.
Bartłomiej KisielDepartment of Internal Diseases and Rheumatology, Military Institute of Medicine, Szaserów 128, 04-141, Warsaw, Poland.
Artur BachtaDepartment of Internal Diseases and Rheumatology, Military Institute of Medicine, Szaserów 128, 04-141, Warsaw, Poland.
Maria FranaszczykDepartment of Medical Biology, Molecular Biology Laboratory, Institute of Cardiology, Alpejska 42, 04-628, Warsaw, Poland.
Dorota Brodowska-KaniaDepartment of Internal Diseases, Nephrology and Dialysis; Military Institute of Medicine, Szaserów 128, 04-141, Warsaw, Poland.
Wawrzyniec ŻmudzkiDepartment of Internal Diseases, Nephrology and Dialysis; Military Institute of Medicine, Szaserów 128, 04-141, Warsaw, Poland.
Konrad SzymańskiDepartment of Medical Genetics, Medical University of Warsaw, Pawińskiego 3c, 02-106, Warsaw, Poland.
Antoni SokalskiNephrology and Dialysis Unit, Hospital in Radom, Lekarska 4, 26-610, Radom, Poland.
Wiesław KlatkoDepartment of Nephrology, Public Hospital in Ciechanów, Powstańców Wielkopolskich 2, 06-400, Ciechanów, Poland.
Marek StopińskiWest Hospital, Daleka 11, 05-825, Grodzisk Mazowiecki, Poland.
Janusz GrochowskiHospital in Maków Mazowiecki, Witosa 2, 06-200, Maków Mazowiecki, Poland.
Marek PaplińskiHospital in Sokołów Podlaski, ks. Bosko 5, 08-300, Sokołów Podlaski, Poland.
Zdzisław GoździkHospital in Skierniewice, Rybickiego 1, 96-100, Skierniewice, Poland.
Longin NiemczykDepartment of Nephrology, Dialysis and Internal Diseases, Warsaw Medical University, Warsaw, Poland.ORCID 0000-0001-9698-9930
Barbara BoberDepartment of Endocrinology and Isotope Therapy, Military Institute of Medicine, Szaserów 128, 04-141, Warsaw, Poland.
Maciej KołodziejDepartment of Endocrinology and Isotope Therapy, Military Institute of Medicine, Szaserów 128, 04-141, Warsaw, Poland.
Witold TłustochowiczDepartment of Internal Diseases and Rheumatology, Military Institute of Medicine, Szaserów 128, 04-141, Warsaw, Poland.
Grzegorz KamińskiDepartment of Endocrinology and Isotope Therapy, Military Institute of Medicine, Szaserów 128, 04-141, Warsaw, Poland.
Rafał PłoskiDepartment of Medical Genetics, Medical University of Warsaw, Pawińskiego 3c, 02-106, Warsaw, Poland.ORCID 0000-0001-6286-5526
Stanisław NiemczykDepartment of Internal Diseases, Nephrology and Dialysis; Military Institute of Medicine, Szaserów 128, 04-141, Warsaw, Poland.
Wojskowy Instytut Medycyny Lotniczej · PLNational Academy of Medicine · USMedical University of Warsaw · PLInstitute of Cardiology · PLPaństwowa Wyższa Szkoła Zawodowa w Ciechanowie · PLRadom College · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genetic factors play a key role in the pathogenesis of atrial fibrillation (AF). We would like to establish an association between previously described single-nucleotide polymorphisms (SNPs) and AF in haemodialysed patients with end-stage kidney disease (ESKD-HD) as well as to assess the cumulative effect of all genotyped SNPs on AF risk. Sixteen SNPs were genotyped in 113 patients with AF-ESKD-HD and in 157 controls: without AF (NAF) and with ESKD-HD. The distribution of the risk alleles was compared in both groups and between different sub-phenotypes. The multilocus genetic risk score (GRS) was calculated to estimate the cumulative risk conferred by all SNPs. Several loci showed a trend toward an association with permanent AF (perm-AF): CAV1, Cx40 and PITX2. However, GRS was significantly higher in the AF and perm-AF groups, as compared to NAF. Three of the tested variables were independently associated with AF: male sex, history of myocardial infarction (MI) and GRS. The GRS, which combined 13 previously described SNPs, showed a significant and independent association with AF in a Polish population of patients with ESKD-HD and concomitant AF. Further studies on larger groups of patients are needed to confirm the associations.

Indexed as

Genetic Predisposition to DiseaseAgedAtrial FibrillationCase-Control StudiesFemaleGenetic LociHumansKidney Failure, ChronicMalePolandPolymorphism, Single NucleotideRisk Factors

Identifiers

PMID29915175
PMCPMC6006310
OpenAlexW2808092625

What OpenQuestion holds

Textmetadata
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.