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STOX1 gene Y153H polymorphism is associated with early-onset preeclampsia in Turkish population.
Pinarbasi, Ergun; Cekin, Nilgun; Bildirici, Aslihan Esra; Akin, Seyda; Yanik, Ali.
Afiliação
  • Pinarbasi E; Cumhuriyet University, Faculty of Medicine, Department of Medical Biology, Sivas, Turkey. Electronic address: epinar@cumhuriyet.edu.tr.
  • Cekin N; Cumhuriyet University, Faculty of Medicine, Department of Medical Biology, Sivas, Turkey.
  • Bildirici AE; Cumhuriyet University, Faculty of Medicine, Department of Medical Biology, Sivas, Turkey.
  • Akin S; Cumhuriyet University, Faculty of Medicine, Department of Medical Biology, Sivas, Turkey.
  • Yanik A; Cumhuriyet University, Faculty of Medicine, Department of Obstetrics and Gynecology, Sivas, Turkey.
Gene ; 754: 144894, 2020 Sep 05.
Article em En | MEDLINE | ID: mdl-32534058
Preeclampsia (PE) is a disease of pregnancy that causes of maternal and prenatal morbidity worldwide. Studies indicate that variations in STOX1 gene may be a direct risk factor to PE but controversial results regarding the relationship of Y153H variation in the second exon of STOX1 gene with PE have been ongoing since 2005. The aim of this study was to identify if there is any correlation between Y153H polymorphisms and PE in Turkish preeclampsia patients. We performed polymerase chain reaction- restriction fragment lengthpolymorphism(PCR-RFLP) analysis in 500 pregnant women, of whom 373 pregnant women with early onset PE (EOPE) and 500 normal pregnant women. The relationship between STOX1 Y153H polymorphism and EOPE/LOPE was evaluated by statistical analysis. We found that STOX1 Y153H polymorphism is a risk factor for EOPE (p = 0.03). The odds ratio was 1,45 (CI 95% = 1,03-2,05). No relationship between STOX1 Y153H polymorphisms and LOPE (p = 0.13) was found. STOX1 gene Y153H polymorphism is associated with the risk ofearly onset of pre-eclampsiain a Turkish population. The results provide further evidence of the role of STOX1 in the pathophysiology of this disease.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Polimorfismo Genético / Pré-Eclâmpsia / Proteínas de Transporte Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Polimorfismo Genético / Pré-Eclâmpsia / Proteínas de Transporte Idioma: En Ano de publicação: 2020 Tipo de documento: Article