Thrombophilia and Recurrent Pregnancy Loss: The Enigma Continues
dc.contributor.author | Barut, Mert Ula | |
dc.contributor.author | Bozkurt, Murat | |
dc.contributor.author | Kahraman, Mehmet | |
dc.contributor.author | Yildirim, Engin | |
dc.contributor.author | Imirzatioglu, Necat | |
dc.contributor.author | Kubar, Ayhan | |
dc.contributor.author | Sak, Sibel | |
dc.date.accessioned | 2024-04-24T17:15:08Z | |
dc.date.available | 2024-04-24T17:15:08Z | |
dc.date.issued | 2018 | |
dc.department | Dicle Üniversitesi | en_US |
dc.description.abstract | Background: Thrombophilic gene polymorphism is known to be a risk factor for recurrent pregnancy loss (RPL), but few studies have confirmed a possible role of thrombophilic genes polymorphism in RPL risk. This study was conducted to understand the relationship of the mutations of some thrombophilia-associated gene polymorphism (heterozygous/homozygous) with RPL. We compared patients with 2 abortions to patients with 3 or more abortions among Turkish women. Material/Methods: In this study, patients previously diagnosed with habitual abortus at Obstetrics and Gynecology outpatient clinics in Turkey between 2012 and 2016 were included. In their peripheral blood, we detected factor V Leiden H1299R, prothrombin G20210A, MTHFR C677T, MTHFR A1298C, PAI-1 4G/5G, and PAI-1 4G/4G gene mutations. Results: In this study, we have observed statistically meaningful data (P<0.01) related to the relationship between RPL and thrombophilia-associated gene polymorphisms such as heterozygous factor V Leiden H1299R, heterozygous prothrombin G20210A, PAI-1 4G/5G, and PAI-1 4G/4G. Conclusions: We found that diagnosis of thrombophilic genes polymorphism is useful to determine the causes of RPL, recognizing that this multifactorial disease can also be influenced by various acquired factors, including reproduction-associated risk factors and prolonged immobilization. | en_US |
dc.identifier.doi | 10.12659/MSM.908832 | |
dc.identifier.endpage | 4294 | en_US |
dc.identifier.issn | 1643-3750 | |
dc.identifier.pmid | 29932168 | |
dc.identifier.scopus | 2-s2.0-85049663652 | |
dc.identifier.scopusquality | Q1 | |
dc.identifier.startpage | 4288 | en_US |
dc.identifier.uri | https://doi.org/10.12659/MSM.908832 | |
dc.identifier.uri | https://hdl.handle.net/11468/18347 | |
dc.identifier.volume | 24 | en_US |
dc.identifier.wos | WOS:000436366600002 | |
dc.identifier.wosquality | Q3 | |
dc.indekslendigikaynak | Web of Science | |
dc.indekslendigikaynak | Scopus | |
dc.indekslendigikaynak | PubMed | |
dc.language.iso | en | en_US |
dc.publisher | Int Scientific Information, Inc | en_US |
dc.relation.ispartof | Medical Science Monitor | |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.subject | Abortion, Habitual | en_US |
dc.subject | Polymorphism, Genetic | en_US |
dc.subject | Thrombophilia | en_US |
dc.title | Thrombophilia and Recurrent Pregnancy Loss: The Enigma Continues | en_US |
dc.title | Thrombophilia and Recurrent Pregnancy Loss: The Enigma Continues | |
dc.type | Article | en_US |