Literature DB >> 27026779

Inherited thrombophilia and reproductive disorders.

Spyros A Liatsikos1, Panagiotis Tsikouras1, Bachar Manav1, Roland Csorba2, Georg Friedrich von Tempelhoff2, Georgios Galazios1.   

Abstract

Apart from its established role in the pathogenesis of venous thromboembolism (VTE), inherited thrombophilia has been proposed as a possible cause of pregnancy loss and vascular gestational complications. There is a lot of controversy in the literature on the relationship between inherited prothrombotic defects and these obstetric complications. This is a review of the literature on inherited thrombophilia and reproductive disorders. Factor V Leiden, prothrombin G20210A mutation, and protein S deficiency seem to be associated with late and recurrent early pregnancy loss, while their impact on other pregnancy complications is conflicting. No definite association has been established between protein C and antithrombin deficiency and adverse pregnancy outcome, primarily due to their low prevalence. Screening is suggested only for women with early recurrent loss or late pregnancy loss. Anticoagulant treatment during pregnancy should be considered for women with complications who were tested positive for thrombophilia.

Entities:  

Keywords:  Inherited thrombophilia; recurrent pregnancy loss; reproductive disorders

Year:  2016        PMID: 27026779      PMCID: PMC4794292          DOI: 10.5152/jtgga.2016.15212

Source DB:  PubMed          Journal:  J Turk Ger Gynecol Assoc        ISSN: 1309-0380


  33 in total

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Review 7.  The association of factor V leiden and prothrombin gene mutation and placenta-mediated pregnancy complications: a systematic review and meta-analysis of prospective cohort studies.

Authors:  Marc A Rodger; Marisol T Betancourt; Peter Clark; Pelle G Lindqvist; Donna Dizon-Townson; Joanne Said; Uri Seligsohn; Marc Carrier; Ophira Salomon; Ian A Greer
Journal:  PLoS Med       Date:  2010-06-15       Impact factor: 11.069

8.  Inherited thrombophilia in infertile women: implication in unexplained infertility.

Authors:  Luisa Casadei; Francesco Puca; Laura Privitera; Valentina Zamaro; Emanuela Emidi
Journal:  Fertil Steril       Date:  2009-11-25       Impact factor: 7.329

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10.  Thrombophilic gene polymorphisms are risk factors for unexplained infertility.

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Journal:  Fertil Steril       Date:  2008-10-17       Impact factor: 7.329

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  3 in total

1.  Combined presence of coagulation factor XIII V34L and plasminogen activator inhibitor 1 4G/5G gene polymorphisms significantly contribute to recurrent pregnancy loss in Serbian population.

Authors:  Ivana Joksic; Zeljko Mikovic; Dejan Filimonovic; Jelena Munjas; Orlic Natasa Karadzov; Amira Egic; Gordana Joksic
Journal:  J Med Biochem       Date:  2020-01-23       Impact factor: 3.402

Review 2.  The obstetric complications in women with hereditary thrombophilia.

Authors:  Diana Mitriuc; Olga Popuşoi; Rodica Catrinici; Valentin Friptu
Journal:  Med Pharm Rep       Date:  2019-04-25

3.  [Clinical manifestations and gene analysis of 18 cases of hereditary protein S deficiency].

Authors:  D L Zhang; F Xue; R F Fu; Y F Chen; X F Liu; W Liu; Y J Jia; H Y Li; Y H Wang; Z J Xiao; L Zhang; R C Yang
Journal:  Zhonghua Xue Ye Xue Za Zhi       Date:  2022-01-14
  3 in total

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