The role of two common FOXP3 gene promoter polymorphisms in preeclampsia in a Turkish population: a case-control study

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dc.contributor.authorCekin, Nilgun
dc.contributor.authorPinarbasi, Ergun
dc.contributor.authorBildirici, Aslihan Esra
dc.contributor.authorHatice
dc.contributor.authorYanik, Ali
dc.contributor.authorSonmez, Gamze
dc.date.accessioned2024-03-13T10:35:20Z
dc.date.available2024-03-13T10:35:20Z
dc.date.issued2020
dc.departmentİstanbul Beykent Üniversitesien_US
dc.description.abstractPreeclampsia (PE), which occurs in approximately 5% of pregnancies worldwide and constitutes clinically serious complications in 2-3%, is one of the leading causes of maternal and prenatal morbidity and mortality. Recent studies report that regulatory T (Treg) cells, which act as immunosuppressant, are associated with PE. It is clearly defined that FOXP3/Scurfin (Forkhead Box P3) is involved in the development and function of Tregs. However, there are different conclusions regarding the relationship between PE and FOXP3 gene polymorphisms for different populations. For this reason, in this study we investigate the association between FOXP3 gene promoter region polymorphisms and PE in a Turkish population 500 PE patients and 500 healthy pregnant women. Blood samples taken from pregnant women were studied by PCR-RFLP method. As a result, rs2232365 polymorphism was significantly associated with disease (p < .0001) while no significant association was found between rs3761548 polymorphism and the disease (p = .17). Based on these results, it is though that FOXP3 rs2232365 polymorphism may be predisposed to PE development in terms of Turkish population. However, further and functional studies are needed in terms of other polymorphisms and mutations.IMPACT STATEMENT What is already known on this subject? A number of recent publications suggest that Tregs may play a role in the pathogenesis of PE. It is known that a stable and high FOXP3 expression is required to maintain the suppressive T cell function of Tregs. Down regulation of FOXP3 in PE has been reported in many previous studies, but the mechanism is still uncertain. What do the results of this study add? Our study has examined two FOXP3 promoter region polymorphisms in terms of Turkish population for the first time. Rs2232365 polymorphism associated with the disease in heterozygous genotype.en_US
dc.identifier.doi10.1080/01443615.2019.1634017
dc.identifier.endpage499en_US
dc.identifier.issn0144-3615
dc.identifier.issn1364-6893
dc.identifier.issue4en_US
dc.identifier.pmid32401107en_US
dc.identifier.scopus2-s2.0-85073935807
dc.identifier.scopusqualityQ3en_US
dc.identifier.startpage495en_US
dc.identifier.urihttps://doi.org/10.1080/01443615.2019.1634017
dc.identifier.urihttps://hdl.handle.net/20.500.12662/4375
dc.identifier.volume40en_US
dc.identifier.wosWOS:000486763500001
dc.identifier.wosqualityQ4en_US
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoenen_US
dc.publisherTaylor & Francis Incen_US
dc.relation.ispartofJournal Of Obstetrics And Gynaecologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectPreeclampsiaen_US
dc.subjectFOXP3en_US
dc.subjectpolymorphismen_US
dc.subjectTregen_US
dc.subjectT cellen_US
dc.titleThe role of two common FOXP3 gene promoter polymorphisms in preeclampsia in a Turkish population: a case-control studyen_US
dc.typeArticleen_US

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