Evidence map›Paper›PMID 34215992›Full record

ArticleMolecular biology reports2021

Prevalence of rare F5 variants in general population from Bosnia and Herzegovina.

Adna Ašić, Ramona Salazar, Niels Storm, Serkan Doğan, Wolfgang Höppner, Damir Marjanović, Dragan Primorac

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular biology reports, 2021. 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
0.1field-weighted citation impact, top 55% 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, 1 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

7 authors at 5 institutions in 4 countries.

Adna AšićDepartment of Genetics and Bioengineering, International Burch University, Francuske revolucije bb, 71000, Sarajevo, Bosnia and Herzegovina. adna.asic@ibu.edu.ba.ORCID http://orcid.org/0000-0001-6197-9572
Ramona SalazarLabor Dr. Heidrich Und Kollegen MVZ GmbH, Stuvkamp 22, 22081, Hamburg, Germany.
Niels StormLabor Dr. Heidrich Und Kollegen MVZ GmbH, Stuvkamp 22, 22081, Hamburg, Germany.
Serkan DoğanDepartment of Genetics and Bioengineering, International Burch University, Francuske revolucije bb, 71000, Sarajevo, Bosnia and Herzegovina.
Wolfgang HöppnerLabor Dr. Heidrich Und Kollegen MVZ GmbH, Stuvkamp 22, 22081, Hamburg, Germany.
Damir MarjanovićDepartment of Genetics and Bioengineering, International Burch University, Francuske revolucije bb, 71000, Sarajevo, Bosnia and Herzegovina.
Dragan PrimoracSt. Catherine Specialty Hospital, Zagreb and Zabok, Croatia.
International Burch University · BAMedizinisches Versorgungszentrum Prof. Mathey, Prof. Schofer · DEBioglobe (Germany) · DELee College · USUniversity of Zagreb · HR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human gene F5, encoding coagulation factor V, was previously reported to be highly polymorphic. Apart from FV Leiden, several other rare variants have been detected in clinical practice and associated with thrombotic events, especially in cases when patient's phenotype and FV Leiden genotype were not in agreement. In this study, the prevalence of 17 rare F5 variants has been studied on a sample of 130 healthy adult individuals from the general Bosnian-Herzegovinian population. DNA was isolated from buccal swab samples, while genotyping was performed using MALDI-TOF MS method. The results have shown that Asp2194Gly and Met2120Thr are polymorphic in the study population with minor allele frequencies of 0.077 and 0.073, respectively. Additionally, these two variants were mutually exclusive with FV Leiden and none of them was positively associated with participants' family history of cardiovascular or cerebrovascular diseases. While the obtained results are in agreement with previously reported data for the general Caucasian populations, it is worth noting that only two rare F5 variants were detected in the study population, albeit at considerable frequencies. Still, scientific information on rare F5 variants is rather scarce and further studies aiming to assess functional importance of these variants, as well as their role as prothrombotic factors are necessary.

Indexed as

AdultBosnia and HerzegovinaDNAFactor VFemaleGenetic VariationGenotypeHealthy VolunteersHumansMaleMicrosatellite RepeatsPolymorphism, Single NucleotidePrevalenceDNAFactor Vfactor V LeidenBosnia and HerzegovinaFactor V Asp2194GlyFactor V LeidenFactor V Met2120ThrRare Factor V variantsThrombophilia

Identifiers

PMID34215992
OpenAlexW3162507035

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.