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Activity of coagulation factor XI in patients with spontaneous miscarriage: the presence of risk alleles.
Sokol, J; Biringer, K; Skerenova, M; Stasko, J; Kubisz, P.
Afiliação
  • Sokol J; a Department of Haematology and Transfusiology , National Center of Haemostasis and Thrombosis, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava , Martin , Slovakia.
  • Biringer K; b Department of Obstetrics and Gynaecology , Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava , Martin , Slovakia.
  • Skerenova M; c Department of Biochemistry , Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava , Martin , Slovakia.
  • Stasko J; a Department of Haematology and Transfusiology , National Center of Haemostasis and Thrombosis, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava , Martin , Slovakia.
  • Kubisz P; a Department of Haematology and Transfusiology , National Center of Haemostasis and Thrombosis, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava , Martin , Slovakia.
J Obstet Gynaecol ; 35(6): 621-4, 2015.
Article em En | MEDLINE | ID: mdl-25517908
The aim of this study was to compare the activity of coagulation factor XI (FXI) between patients with spontaneous miscarriage versus control group with no history of miscarriage and thrombosis, and then we evaluated the occurrence of risk alleles in the relation to miscarriage. FXI activity was determined using a coagulometer (Sysmex, CA 1500, Japan). Single nucleotide polymorphisms (SNPs) of F11 and CYP4V2 genes were evaluated. We examined 55 patients versus 31 control subjects. We found significantly higher activity of FXI (p = 0.04) in patients versus control subjects. The occurrence of two SNPs (rs2289252 and rs2036914) of the F11 gene and SNP (rs13146272) of CYP4V2 gene was not significantly different between both groups. Increased activity of FXI may be a potential risk factor for miscarriage. High activity of FXI diagnosed in women with history of miscarriage is not probably caused by the presence of studied SNPs.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fator XI / Aborto Espontâneo / Polimorfismo de Nucleotídeo Único Tipo de estudo: Etiology_studies / Risk_factors_studies Limite: Adult / Female / Humans / Pregnancy Idioma: En Revista: J Obstet Gynaecol Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Eslováquia

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fator XI / Aborto Espontâneo / Polimorfismo de Nucleotídeo Único Tipo de estudo: Etiology_studies / Risk_factors_studies Limite: Adult / Female / Humans / Pregnancy Idioma: En Revista: J Obstet Gynaecol Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Eslováquia