Evidence map›Paper›PMID 22562116›Full record

Trial reportJournal of thrombosis and thrombolysis2012

The frequency of factor V Leiden and prothrombin G20210A mutations in Slovak and Roma (Gypsy) ethnic group of Eastern Slovakia.

Alexandra Bôžiková, Dana Gabriková, Adriana Sovičová, Regina Behulová, Soňa Mačeková, Iveta Boroňová, Eva Petrejčíková, Miroslav Soták, Jarmila Bernasovská, Ivan Bernasovský

Abstract readClinical TrialComparative Study
PubMed Publisher
In one paragraph

Trial report in Journal of thrombosis and thrombolysis, 2012. 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
0.5field-weighted citation impact, top 34% 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, 9 citations in OpenAlex.

  1. Neurology · 2017
    Article
  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

10 authors at 1 institution in 1 country.

Alexandra BôžikováExcellence Centre of Animal and Human Ecology, Faculty of Humanities and Natural Sciences, University of Prešov, 17 Novembra 1, 08116, Prešov, Slovakia. bozikova@unipo.sk
Dana Gabriková
Adriana Sovičová
Regina Behulová
Soňa Mačeková
Iveta Boroňová
Eva Petrejčíková
Miroslav Soták
Jarmila Bernasovská
Ivan Bernasovský
University of Prešov · SK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Factor V Leiden and prothrombin G20210A are the two most prevalent causes of inherited thrombophilia. The prevalence of these mutations varies widely in healthy Caucasian population. The aim of our study was to determine the frequency of factor V Leiden and prothrombin G20210A mutations in Slovak and Roma ethnic group from Eastern Slovakia. We analyzed 540 asymptomatic individuals (269 individuals of Slovak ethnicity and 271 individuals of Roma ethnicity) by real-time PCR method. The detected allele frequencies were 2.97 versus 6.64 % for factor V Leiden (p = 0.0049), and 0.74 versus 0.92 % for prothrombin mutation (p = 0.7463) in Slovak and Roma population, respectively. The Roma ethnic group had significantly higher prevalence of factor V Leiden mutation when compared to Slovak ethnic group. The allele frequency of factor V Leiden in ethnic Romanies from Eastern Slovakia was one of the highest in Europe. Our results confirm an uneven geographical and ethnic distribution of factor V Leiden.

Indexed as

Romani PeopleActivated Protein C ResistanceAdultAllelesAmino Acid SubstitutionFactor VFemaleGene FrequencyHumansMaleMutation, MissenseProthrombinSlovakiaThrombophiliaFactor Vfactor V LeidenProthrombin

Identifiers

PMID22562116
OpenAlexW1982282060

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.