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Is enoxaparin necessary to prevent adverse pregnancy outcomes in ethylenetetrahydrofolate reductase polymorphism positive recurrent pregnancy loss cases?

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dc.contributor.author ÇOŞKUN, Ebru İnci
dc.contributor.author SAGER, Hakan
dc.contributor.author SANCAK, Muhammed Emin
dc.contributor.author DİNÇGEZ ÇAKMAK, Burcu
dc.contributor.author ÖZTAŞ, Sonay
dc.contributor.author UZSEZER, Begüm
dc.date.accessioned 2022-11-10T13:02:46Z
dc.date.available 2022-11-10T13:02:46Z
dc.date.issued 2020
dc.identifier.citation SAGER H, SANCAK M, ÇAKMAK B, ÖZTAŞ S, UZSEZER B, ÇOŞKUN E (2020). Is enoxaparin necessary to prevent adverse pregnancy outcomes in ethylenetetrahydrofolate reductase polymorphism positive recurrent pregnancy loss cases?. Medicine Science, 9(3), 646 - 652. 10.5455/medscience.2020.06.117 en_US
dc.identifier.uri http://hdl.handle.net/11616/85262
dc.description.abstract The association between methylenetetrahydrofolate reductase polymorphism and recurrent pregnancy loss is still under debate. Moreover, the use of enoxaparin to preventadverse pregnancy outcomes is controversial in these patients. We aimed to analyse the effect of enoxaparin on pregnancy outcomes in recurrent pregnancy loss withonly methylenetetrahydrofolate reductase gene polymorphism. A total of 339 pregnant women with recurrent pregnancy loss and methylenetetrahydrofolate reductasegene polymorphism between June 2017 and March 2019 were included. Patients were divided into two groups: enoxaparin plus folic acid (n=165) and folic acid group(n=174). Then, these groups were divided into subgroups: MTHFR A1298C homozygous (n=52), MTHFR A1298C heterozygous (n=141), MTHFR C677T homozygous(n=56) and MTHFR C677T heterozygous (n=90). Pregnancy outcomes were recorded and compared between two main group, and also between subgroups. There wasno significant difference between enoxaparin plus folic acid group and only folic acid group according to delivery week (p=0.287), birthweight (p=0.677), miscarriage(p=0.372), stillbirth (p=0.585), live birth (p=0.246), preterm birth (p=0.700), anomaly (p=0.883), preeclampsia (p=0.656), intrauterine growth restriction (p=0.764), neonatal intensive care unit admission (p=0.820), APGAR 1st minutes<7 (p=0.729), APGAR 5th minutes<7 (p=1.000) and cesarean delivery (p=0.540). Furthermore therewas no statistically significant difference with regard to delivery week, birthweight, miscarriage, stillbirth, live birth, preterm birth, anomaly, preeclampsia, intrauterinegrowth restriction, neonatal intensive care unit admission, APGAR 1st minute <7, APGAR 5th minute <7 and cesarean delivery between each subgroups. Contrary to theincreasing trend of using empirical therapy with low molecular weight heparin in Turkey, we firstly demonstrated that there is no necessity to use enoxaparin to improvepregnancy outcomes both in homozygous and heterozygous methylenetetrahydrofolate reductase polymorphism related pregnancy loss cases. We suggest that only folicacid is enough for these cases. en_US
dc.language.iso eng en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.title Is enoxaparin necessary to prevent adverse pregnancy outcomes in ethylenetetrahydrofolate reductase polymorphism positive recurrent pregnancy loss cases? en_US
dc.type article en_US
dc.relation.journal Medicine Science en_US
dc.contributor.department İnönü Üniversitesi en_US


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