Literature DB >> 22562116

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

Alexandra Bôžiková1, Dana Gabriková, Adriana Sovičová, Regina Behulová, Soňa Mačeková, Iveta Boroňová, Eva Petrejčíková, Miroslav Soták, Jarmila Bernasovská, Ivan Bernasovský.   

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.

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Year:  2012        PMID: 22562116     DOI: 10.1007/s11239-012-0736-4

Source DB:  PubMed          Journal:  J Thromb Thrombolysis        ISSN: 0929-5305            Impact factor:   2.300


  26 in total

1.  High frequency of factor V Leiden mutation and prothrombin 20210A variant in Romanies of Eastern Hungary.

Authors:  I Balogh; R Póka; G Losonczy; L Muszbek
Journal:  Thromb Haemost       Date:  1999-11       Impact factor: 5.249

Review 2.  Risk factors for venous thrombotic disease.

Authors:  F R Rosendaal
Journal:  Thromb Haemost       Date:  1999-08       Impact factor: 5.249

3.  Born to clot: the European burden.

Authors:  D C Rees; N H Chapman; M T Webster; J F Guerreiro; J Rochette; J B Clegg
Journal:  Br J Haematol       Date:  1999-05       Impact factor: 6.998

4.  High frequency of factor V Leiden mutation in Parsis--a highly endogamous population in India.

Authors:  A Pawar; K Ghosh; S Shetty; R Colah; D Mohanty
Journal:  Thromb Haemost       Date:  2000-06       Impact factor: 5.249

5.  Geography too determines the causes of inherited thrombophilia.

Authors:  K Ghosh; A Khare; B Kulkarni; S Shetty; D Mohanty
Journal:  J Thromb Haemost       Date:  2004-02       Impact factor: 5.824

6.  A single genetic origin for the common prothrombotic G20210A polymorphism in the prothrombin gene.

Authors:  A Zivelin; N Rosenberg; S Faier; N Kornbrot; H Peretz; C Mannhalter; M H Horellou; U Seligsohn
Journal:  Blood       Date:  1998-08-15       Impact factor: 22.113

7.  [The factor V Leiden mutation in users of hormonal contraceptives].

Authors:  J Paseka; V Unzeitig; D Cibula; A Buliková; M Matýsková; K Chroust
Journal:  Ceska Gynekol       Date:  2000-05

8.  Matched case-control study on factor V Leiden and the prothrombin G20210A mutation in patients with ischemic stroke/transient ischemic attack up to the age of 60 years.

Authors:  Wolfgang Lalouschek; Martin Schillinger; Kety Hsieh; Georg Endler; Susanne Tentschert; Wilfried Lang; Suzanne Cheng; Christine Mannhalter
Journal:  Stroke       Date:  2005-06-09       Impact factor: 7.914

9.  World distribution of factor V Leiden.

Authors:  D C Rees; M Cox; J B Clegg
Journal:  Lancet       Date:  1995-10-28       Impact factor: 79.321

10.  The G1691A mutation of the factor V gene (factor V Leiden) and the G20210A mutation of the prothrombin gene as risk factors in thrombotic microangiopathies.

Authors:  Christoph Sucker; Christine Kurschat; Gerd R Hetzel; Bernd Grabensee; Beate Maruhn-Debowski; Robert Loncar; Ljerka Ostojic; Ruediger E Scharf; Rainer B Zotz
Journal:  Clin Appl Thromb Hemost       Date:  2009 May-Jun       Impact factor: 2.389

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  3 in total

1.  Ethnic differences in the association of thrombophilic polymorphisms with obstetric complications in Slovak and Roma (Gypsy) populations.

Authors:  Alexandra Bozikova; Dana Gabrikova; Jozef Pitonak; Jarmila Bernasovska; Sona Macekova; Regina Lohajova-Behulova
Journal:  Genet Test Mol Biomarkers       Date:  2014-12-30

2.  MARVELD2 (DFNB49) mutations in the hearing impaired Central European Roma population--prevalence, clinical impact and the common origin.

Authors:  Ivica Mašindová; Andrea Šoltýsová; Lukáš Varga; Petra Mátyás; Andrej Ficek; Miloslava Hučková; Martina Sůrová; Dana Šafka-Brožková; Saima Anwar; Judit Bene; Slavomír Straka; Ingrid Janicsek; Zubair M Ahmed; Pavel Seeman; Béla Melegh; Milan Profant; Iwar Klimeš; Saima Riazuddin; Ľudevít Kádasi; Daniela Gašperíková
Journal:  PLoS One       Date:  2015-04-17       Impact factor: 3.240

3.  UFM1 founder mutation in the Roma population causes recessive variant of H-ABC.

Authors:  Eline M C Hamilton; Enrico Bertini; Luba Kalaydjieva; Bharti Morar; Dana Dojčáková; Judy Liu; Adeline Vanderver; Julian Curiel; Claudia M Persoon; Daria Diodato; Lorenzo Pinelli; Nathalie L van der Meij; Barbara Plecko; Susan Blaser; Nicole I Wolf; Quinten Waisfisz; Truus E M Abbink; Marjo S van der Knaap
Journal:  Neurology       Date:  2017-09-20       Impact factor: 9.910

  3 in total

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