Literature DB >> 17572893

Factor V Leiden and G20210A prothrombin mutations in patients with recurrent pregnancy loss: data from the southeast of Turkey.

Abdullah Altintas1, Semir Pasa, Nurten Akdeniz, Timucin Cil, Murat Yurt, Orhan Ayyildiz, Sabri Batun, Hilmi Isi.   

Abstract

Factor V Leiden (FV-Leiden) and prothrombin gene mutations (FII G20210A) are well-established independent risk factors for thrombosis. In the recent years, many studies have suggested that these mutations are associated with an increased risk of recurrent pregnancy loss (RPL). We aimed to investigate the prevalence of these molecular defects in subjects with a history of early RPL. One hundred and fourteen women with three or more consecutive unexplained first-trimester miscarriages were compared to 185 parous women with uncomplicated pregnancies from the same ethnic origin. The presence of FV-Leiden and FII G20210A mutations was assessed by polymerase chain reaction analysis. Overall, 11 out of the 114 women with early RPL (9.6%) had either FV-Leiden or FII G20210A mutation, as compared with 16 out of the 185 women with normal pregnancies (8.6%; p = 0.756). The prevalence of FV-Leiden mutation was 7.9% (9/114) in patient group, compared with 7% (13/185) in control group (p = 0.780). One hundred and two patients were primary and 12 were secondary aborters. All FV-Leiden positive cases were primary aborters (8.8%; 9/102, p = 0.584). Concerning the FII G20210A, two out of 114 (1.7%) were first-trimester RPL (primary aborters) and three out of 185 (1.6%) controls were carriers of the FII G20210A mutation (1.7 vs 1.6%, p = 0.931). The results obtained from patients with first-trimester RPL and the control group have no statistical significant differences in the prevalence of FV-Leiden and FII G20210A mutations. These results suggest that mutations have no role in etiology of first-trimester recurrent abortions.

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Year:  2007        PMID: 17572893     DOI: 10.1007/s00277-007-0327-1

Source DB:  PubMed          Journal:  Ann Hematol        ISSN: 0939-5555            Impact factor:   3.673


  14 in total

1.  Evaluation of GenoFlow Thrombophilia Array Test Kit in its detection of mutations in Factor V Leiden (G1691A), prothrombin G20210A, MTHFR C677T and A1298C in blood samples from 113 Turkish female patients.

Authors:  Ebru Aytekin; Sezen Guntekin Ergun; Mehmet Ali Ergun; Ferda E Percin
Journal:  Genet Test Mol Biomarkers       Date:  2014-08-25

2.  The association between thrombophilic gene mutations and recurrent pregnancy loss.

Authors:  Ahmad Poursadegh Zonouzi; Nader Chaparzadeh; Saeid Ghorbian; Mahzad Mehrzad Sadaghiani; Laya Farzadi; Alieh Ghasemzadeh; Taiebeh Kafshdooz; Masoud Sakhinia; Ebrahim Sakhinia
Journal:  J Assist Reprod Genet       Date:  2013-08-29       Impact factor: 3.412

3.  Prevalence of 1691G>A FV mutation in females from Bosnia and Herzegovina--a preliminary report.

Authors:  Amina Valjevac; Bakir Mehić; Emina Kiseljaković; Slavka Ibrulj; Agnieszka Garstka; Grażyna Adler
Journal:  Bosn J Basic Med Sci       Date:  2013-02       Impact factor: 3.363

4.  Prevalence of F5 1691G>A, F2 20210G>A, and MTHFR 677C>T polymorphisms in Bosnian women with pregnancy loss.

Authors:  Emir Mahmutbegović; Damir Marjanović; Edin Medjedović; Nevena Mahmutbegović; Serkan Dogan; Amina Valjevac; Ewa Czerska; Anna Pawińska-Matecka; Agnieszka Madlani; Grażyna Adler
Journal:  Bosn J Basic Med Sci       Date:  2017-11-20       Impact factor: 3.363

5.  A Multiplex Allele Specific Polymerase Chain Reaction (MAS-PCR) for the Detection of Factor V Leiden and Prothrombin G20210A.

Authors:  Morteza Bagheri; Isa Abdi Rad
Journal:  Maedica (Buchar)       Date:  2011-01

6.  Thrombophilia screening in women with recurrent first trimester miscarriage: is it time to stop testing? - a cohort study and systematic review of the literature.

Authors:  Hassan Shehata; Amanda Ali; Mariane Silva-Edge; Shahla Haroon; Abdullatif Elfituri; Radhika Viswanatha; Haider Jan; Ranjit Akolekar
Journal:  BMJ Open       Date:  2022-07-13       Impact factor: 3.006

7.  Association between apolipoprotein E gene polymorphism and the risk of recurrent pregnancy loss: a meta-analysis.

Authors:  Hai-xia Meng; Mu-ge Qi; Yuan-yuan Yi; Ya-ping Liu
Journal:  J Assist Reprod Genet       Date:  2013-10-20       Impact factor: 3.412

8.  Evaluation of Factor V G1691A, prothrombin G20210A, Factor XIII V34L, MTHFR A1298C, MTHFR C677T and PAI-1 4G/5G genotype frequencies of patients subjected to cardiovascular disease (CVD) panel in south-east region of Turkey.

Authors:  Serdar Oztuzcu; Sercan Ergun; Mustafa Ulaşlı; Gülper Nacarkahya; Yusuf Ziya Iğci; Mehri Iğci; Recep Bayraktar; Ali Tamer; Ecir Ali Çakmak; Ahmet Arslan
Journal:  Mol Biol Rep       Date:  2014-02-15       Impact factor: 2.316

9.  Prothrombin gene G20210A mutation and obstetric complications.

Authors:  Robert M Silver; Yuan Zhao; Catherine Y Spong; Baha Sibai; George Wendel; Katharine Wenstrom; Philip Samuels; Steve N Caritis; Yoram Sorokin; Menachem Miodovnik; Mary J O'Sullivan; Deborah Conway; Ronald J Wapner
Journal:  Obstet Gynecol       Date:  2010-01       Impact factor: 7.623

10.  Inherited thrombophilia and recurrent pregnancy loss.

Authors:  Alireza Parand; Jale Zolghadri; Mozhgan Nezam; Abdolreza Afrasiabi; Sezaneh Haghpanah; Mehran Karimi
Journal:  Iran Red Crescent Med J       Date:  2013-12-05       Impact factor: 0.611

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